IL34314A - O-alkyl(or cycloalkyl)-s-(n,n-dialkylaminocarbamylmethyl)esters of alkyl-and aryl-thiolphosphonic and-thionothiolphosphonic acids,their preparation and use as insecticides and acaricides - Google Patents

O-alkyl(or cycloalkyl)-s-(n,n-dialkylaminocarbamylmethyl)esters of alkyl-and aryl-thiolphosphonic and-thionothiolphosphonic acids,their preparation and use as insecticides and acaricides

Info

Publication number: IL34314A
Authority: IL; Israel
Prior art keywords: alkyl; stands; compound; formula; compound according
Prior art date: 1969-04-23

Application number

IL7034314A

Other languages

English (en)

Other versions

IL34314A0 (en

Original Assignee

Bayer Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1969-04-23

Filing date

1970-04-14

Publication date

1972-12-29

1970-04-14 Application filed by Bayer Ag filed Critical Bayer Ag

1970-06-17 Publication of IL34314A0 publication Critical patent/IL34314A0/xx

1972-12-29 Publication of IL34314A publication Critical patent/IL34314A/en

Links

239000002253 acid Substances 0.000 title claims description 9
125000000753 cycloalkyl group Chemical group 0.000 title claims description 5
150000002148 esters Chemical class 0.000 title claims 2
238000002360 preparation method Methods 0.000 title description 18
230000000895 acaricidal effect Effects 0.000 title description 6
239000002917 insecticide Substances 0.000 title description 5
239000000642 acaricide Substances 0.000 title description 3
150000007513 acids Chemical class 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims description 64
239000002904 solvent Substances 0.000 claims description 20
-1 alkali metal salt Chemical class 0.000 claims description 13
125000000217 alkyl group Chemical group 0.000 claims description 12
239000003085 diluting agent Substances 0.000 claims description 11
241000238631 Hexapoda Species 0.000 claims description 10
241000607479 Yersinia pestis Species 0.000 claims description 10
238000000034 method Methods 0.000 claims description 10
239000000203 mixture Substances 0.000 claims description 10
239000007788 liquid Substances 0.000 claims description 9
239000007787 solid Substances 0.000 claims description 9
238000006243 chemical reaction Methods 0.000 claims description 8
230000006378 damage Effects 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 6
239000004480 active ingredient Substances 0.000 claims description 4
229910052783 alkali metal Inorganic materials 0.000 claims description 4
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
230000000749 insecticidal effect Effects 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
239000005864 Sulphur Substances 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
150000001342 alkaline earth metals Chemical class 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
150000003863 ammonium salts Chemical class 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
IFQMTQSXPWHEEG-UHFFFAOYSA-N thiophen-2-ylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CS1 IFQMTQSXPWHEEG-UHFFFAOYSA-N 0.000 claims description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
241000238876 Acari Species 0.000 description 13
239000003995 emulsifying agent Substances 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
241000255925 Diptera Species 0.000 description 11
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
244000046052 Phaseolus vulgaris Species 0.000 description 10
241001454295 Tetranychidae Species 0.000 description 10
241001454293 Tetranychus urticae Species 0.000 description 10
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
239000000047 product Substances 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
240000007124 Brassica oleracea Species 0.000 description 6
241000254173 Coleoptera Species 0.000 description 6
239000012141 concentrate Substances 0.000 description 6
241000257159 Musca domestica Species 0.000 description 5
241000488583 Panonychus ulmi Species 0.000 description 5
241001414989 Thysanoptera Species 0.000 description 5
239000000969 carrier Substances 0.000 description 5
238000011156 evaluation Methods 0.000 description 5
238000009472 formulation Methods 0.000 description 5
241000256118 Aedes aegypti Species 0.000 description 4
241001124076 Aphididae Species 0.000 description 4
241000257163 Calliphora vicina Species 0.000 description 4
241000254137 Cicadidae Species 0.000 description 4
241000256059 Culex pipiens Species 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
239000004606 Fillers/Extenders Substances 0.000 description 4
241000721621 Myzus persicae Species 0.000 description 4
241001608567 Phaedon cochleariae Species 0.000 description 4
241001396980 Phytonemus pallidus Species 0.000 description 4
241000952063 Polyphagotarsonemus latus Species 0.000 description 4
241001494115 Stomoxys calcitrans Species 0.000 description 4
125000002877 alkyl aryl group Chemical group 0.000 description 4
229920000151 polyglycol Polymers 0.000 description 4
239000010695 polyglycol Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
235000011303 Brassica alboglabra Nutrition 0.000 description 3
235000011302 Brassica oleracea Nutrition 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
241000500437 Plutella xylostella Species 0.000 description 3
235000001537 Ribes X gardonianum Nutrition 0.000 description 3
235000001535 Ribes X utile Nutrition 0.000 description 3
235000016919 Ribes petraeum Nutrition 0.000 description 3
244000281247 Ribes rubrum Species 0.000 description 3
235000002355 Ribes spicatum Nutrition 0.000 description 3
241000254179 Sitophilus granarius Species 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000003513 alkali Substances 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 3
239000008187 granular material Substances 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
239000006072 paste Substances 0.000 description 3
239000002689 soil Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
241001143309 Acanthoscelides obtectus Species 0.000 description 2
241000238818 Acheta domesticus Species 0.000 description 2
241000426834 Aegina Species 0.000 description 2
241001414900 Anopheles stephensi Species 0.000 description 2
241001425390 Aphis fabae Species 0.000 description 2
241000387321 Aspidiotus nerii Species 0.000 description 2
241001510109 Blaberus giganteus Species 0.000 description 2
241000238657 Blattella germanica Species 0.000 description 2
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
241001444260 Brassicogethes aeneus Species 0.000 description 2
241001221118 Cecidophyopsis ribis Species 0.000 description 2
241000255579 Ceratitis capitata Species 0.000 description 2
241001327638 Cimex lectularius Species 0.000 description 2
241001581006 Dysaphis plantaginea Species 0.000 description 2
241000239245 Euscelis Species 0.000 description 2
241000255896 Galleria mellonella Species 0.000 description 2
241001659688 Hercinothrips femoralis Species 0.000 description 2
241001251909 Hyalopterus pruni Species 0.000 description 2
241000257303 Hymenoptera Species 0.000 description 2
241000256602 Isoptera Species 0.000 description 2
241000810465 Myzus cerasi cerasi Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
241000238887 Ornithodoros Species 0.000 description 2
241001481099 Ornithodoros turicata Species 0.000 description 2
241000257149 Phormia Species 0.000 description 2
241000257186 Phormia regina Species 0.000 description 2
241000255969 Pieris brassicae Species 0.000 description 2
241000500439 Plutella Species 0.000 description 2
241000722238 Pseudococcus maritimus Species 0.000 description 2
241000125167 Rhopalosiphum padi Species 0.000 description 2
241001510241 Rhyparobia Species 0.000 description 2
241000254154 Sitophilus zeamais Species 0.000 description 2
241000256251 Spodoptera frugiperda Species 0.000 description 2
241001177161 Stegobium paniceum Species 0.000 description 2
241001238451 Tortrix viridana Species 0.000 description 2
241000267822 Trogoderma granarium Species 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
238000007098 aminolysis reaction Methods 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
239000004927 clay Substances 0.000 description 2
238000010410 dusting Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
230000002045 lasting effect Effects 0.000 description 2
201000004792 malaria Diseases 0.000 description 2
239000011707 mineral Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000758 substrate Substances 0.000 description 2
230000009885 systemic effect Effects 0.000 description 2
239000002023 wood Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
150000003738 xylenes Chemical class 0.000 description 2
RXXCIBALSKQCAE-UHFFFAOYSA-N 3-methylbutoxymethylbenzene Chemical compound CC(C)CCOCC1=CC=CC=C1 RXXCIBALSKQCAE-UHFFFAOYSA-N 0.000 description 1
241000253994 Acyrthosiphon pisum Species 0.000 description 1
241001136265 Agriotes Species 0.000 description 1
241001136249 Agriotes lineatus Species 0.000 description 1
241000449794 Alabama argillacea Species 0.000 description 1
241000238805 Blaberus Species 0.000 description 1
241000238788 Blaberus craniifer Species 0.000 description 1
241000238659 Blatta Species 0.000 description 1
241000238662 Blatta orientalis Species 0.000 description 1
241001674044 Blattodea Species 0.000 description 1
241000256593 Brachycaudus schwartzi Species 0.000 description 1
241000907225 Bruchidius Species 0.000 description 1
241000042459 Byturus aestivus Species 0.000 description 1
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 1
241001415288 Coccidae Species 0.000 description 1
241001465977 Coccoidea Species 0.000 description 1
241001479447 Coccus hesperidum Species 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241001094913 Cryptomyzus Species 0.000 description 1
241001641895 Dermestes Species 0.000 description 1
241001513837 Dermestes maculatus Species 0.000 description 1
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
241001425477 Dysdercus Species 0.000 description 1
241000630736 Ephestia Species 0.000 description 1
241000122098 Ephestia kuehniella Species 0.000 description 1
241001331999 Euproctis Species 0.000 description 1
241000483001 Euproctis chrysorrhoea Species 0.000 description 1
241000953886 Fannia canicularis Species 0.000 description 1
241000258937 Hemiptera Species 0.000 description 1
241001659689 Hercinothrips Species 0.000 description 1
241000256686 Lasius <genus> Species 0.000 description 1
241000255777 Lepidoptera Species 0.000 description 1
241000258916 Leptinotarsa decemlineata Species 0.000 description 1
241000012186 Litura Species 0.000 description 1
241000721703 Lymantria dispar Species 0.000 description 1
241000721715 Macrosiphum Species 0.000 description 1
241000721714 Macrosiphum euphorbiae Species 0.000 description 1
241000254071 Melolontha Species 0.000 description 1
241000254099 Melolontha melolontha Species 0.000 description 1
241001508687 Mustela erminea Species 0.000 description 1
241000721623 Myzus Species 0.000 description 1
241000359016 Nephotettix Species 0.000 description 1
241001491877 Operophtera brumata Species 0.000 description 1
241000238814 Orthoptera Species 0.000 description 1
241000131102 Oryzaephilus Species 0.000 description 1
241000131101 Oryzaephilus surinamensis Species 0.000 description 1
241001548358 Parapiesma quadratum Species 0.000 description 1
241000238675 Periplaneta americana Species 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
241000690748 Piesma Species 0.000 description 1
235000005805 Prunus cerasus Nutrition 0.000 description 1
241001097374 Pselliopus cinctus Species 0.000 description 1
241000722249 Rhodnius prolixus Species 0.000 description 1
241001510236 Rhyparobia maderae Species 0.000 description 1
241000254105 Tenebrio Species 0.000 description 1
241000254109 Tenebrio molitor Species 0.000 description 1
241001454294 Tetranychus Species 0.000 description 1
241001414831 Triatoma infestans Species 0.000 description 1
241000254113 Tribolium castaneum Species 0.000 description 1
240000006677 Vicia faba Species 0.000 description 1
235000010749 Vicia faba Nutrition 0.000 description 1
241000289690 Xenarthra Species 0.000 description 1
241001466337 Yponomeuta Species 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229960001701 chloroform Drugs 0.000 description 1
239000002274 desiccant Substances 0.000 description 1
229960001760 dimethyl sulfoxide Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
238000003958 fumigation Methods 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
238000002955 isolation Methods 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
230000005923 long-lasting effect Effects 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
230000001473 noxious effect Effects 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
UEWYUCGVQMZMGY-UHFFFAOYSA-N phenyl 2-bromoacetate Chemical compound BrCC(=O)OC1=CC=CC=C1 UEWYUCGVQMZMGY-UHFFFAOYSA-N 0.000 description 1
AGUWUIVKDXDKBT-UHFFFAOYSA-N phenyl 2-chloroacetate Chemical compound ClCC(=O)OC1=CC=CC=C1 AGUWUIVKDXDKBT-UHFFFAOYSA-N 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000001119 rodenticidal effect Effects 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000009834 vaporization Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000002699 waste material Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4075—Esters with hydroxyalkyl compounds

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Molecular Biology (AREA)
Agronomy & Crop Science (AREA)
Biochemistry (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

IL7034314A 1969-04-23 1970-04-14 O-alkyl(or cycloalkyl)-s-(n,n-dialkylaminocarbamylmethyl)esters of alkyl-and aryl-thiolphosphonic and-thionothiolphosphonic acids,their preparation and use as insecticides and acaricides IL34314A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19691920504 DE1920504A1 (de)	1969-04-23	1969-04-23	Alkyl- und Aryl-(thiono)-thiolphosphon-saeure-O-alkyl-S-(N,N-dialkylamino-carbamyl)-methylester und Verfahren zu ihrer Herstellung

Publications (2)

Publication Number	Publication Date
IL34314A0 IL34314A0 (en)	1970-06-17
IL34314A true IL34314A (en)	1972-12-29

Family

ID=5731988

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL7034314A IL34314A (en)	1969-04-23	1970-04-14	O-alkyl(or cycloalkyl)-s-(n,n-dialkylaminocarbamylmethyl)esters of alkyl-and aryl-thiolphosphonic and-thionothiolphosphonic acids,their preparation and use as insecticides and acaricides

Country Status (13)

Country	Link
US (1)	US3705927A (de)
AT (1)	AT299616B (de)
AU (1)	AU1402270A (de)
BE (1)	BE749408A (de)
CH (1)	CH530165A (de)
DE (1)	DE1920504A1 (de)
DK (1)	DK125329B (de)
ES (1)	ES378901A1 (de)
FR (1)	FR2039415A1 (de)
GB (1)	GB1302782A (de)
IL (1)	IL34314A (de)
NL (1)	NL7005858A (de)
ZA (1)	ZA702653B (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1920506A1 (de) *	1969-04-23	1970-11-05	Bayer Ag	Phosphorylierte bzw. phosphonylierte Derivate von in 2-Stellung alkyl-und/oder aryl-substituierten 2-Mercaptoessigsaeure-N',N' -dialkylhydraziden und Verfahren zu ihrer Herstellung

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3518327A (en) *	1967-04-10	1970-06-30	Stauffer Chemical Co	Phosphoro and phosphono acetylhydrazides

1969
- 1969-04-23 DE DE19691920504 patent/DE1920504A1/de active Pending
1970
- 1970-04-14 IL IL7034314A patent/IL34314A/en unknown
- 1970-04-15 CH CH561870A patent/CH530165A/de not_active IP Right Cessation
- 1970-04-17 AU AU14022/70A patent/AU1402270A/en not_active Expired
- 1970-04-20 US US30311A patent/US3705927A/en not_active Expired - Lifetime
- 1970-04-21 ZA ZA702653A patent/ZA702653B/xx unknown
- 1970-04-22 ES ES378901A patent/ES378901A1/es not_active Expired
- 1970-04-22 NL NL7005858A patent/NL7005858A/xx unknown
- 1970-04-22 GB GB1932470A patent/GB1302782A/en not_active Expired
- 1970-04-22 AT AT366570A patent/AT299616B/de not_active IP Right Cessation
- 1970-04-22 DK DK203870AA patent/DK125329B/da unknown
- 1970-04-23 FR FR7014918A patent/FR2039415A1/fr not_active Withdrawn
- 1970-04-23 BE BE749408D patent/BE749408A/xx unknown

Also Published As

Publication number	Publication date
DK125329B (da)	1973-02-05
CH530165A (de)	1972-11-15
ZA702653B (en)	1971-01-27
US3705927A (en)	1972-12-12
BE749408A (fr)	1970-10-23
AT299616B (de)	1972-06-26
FR2039415A1 (de)	1971-01-15
ES378901A1 (es)	1972-08-01
NL7005858A (de)	1970-10-27
GB1302782A (de)	1973-01-10
IL34314A0 (en)	1970-06-17
DE1920504A1 (de)	1970-11-05
AU1402270A (en)	1971-10-21

Publication	Publication Date	Title
IL46172A (en)	1977-12-30	Pyrimidine Acid Esters - Olephosphoric Theones, Their Preparation and Use as Insecticides and Mites
IL47958A (en)	1977-08-31	Pyrimidinylthionophosphonic acid esters process for their preparation and insecticidal acaricidal and nematicidal compositions containing them
IL34985A (en)	1972-11-28	Triazolothiazole esters of phosphoric, phosphonic and phosphonic acids and of the appropriate tionic acids, their preparation and use as insecticides and acaricides
IL34950A (en)	1973-01-30	Esters of thiazolo-phosphoric and -phosphonic,thiazolo-thionophosphoric and -thionophosphonic acid,their preparation and use as insecticides and acaricides
US4001404A (en)	1977-01-04	N-dithiophosphoryl-carbamic acid esters
IL31318A (en)	1972-04-27	Phosphoric,phosphonic or thionophosphoric(-phosphonic)acid esters of pyridazinediol,their preparation and pest control compositions containing them
US3862268A (en)	1975-01-21	O-alkyl-s-(carbamoyloxy-methyl)-(thiono) thiolphosphoric (phosphonic) acid esters
IL31640A (en)	1972-12-29	Thionophosphonic acid esters,their preparation and use for pest control
US3980783A (en)	1976-09-14	O-Alkyl-S-[3-oxo-triazolo-(4,3-α-pyridin(2)yl-methyl]-(thiono)thiol-phosphoric(phosphonic) acid esters and ester-amides
IL34101A (en)	1972-12-29	O-alkyl-s-(n,n-dialkylaminocarbamyl)-methyl-n-monoalkylamido-thiolphosphoric and thionothiolphosphoric acid esters,their preparation and use as insecticides and acaricides
US3974171A (en)	1976-08-10	O-[3-methyl-1,3,4-triazole-(2,3,-b)-thiazol(6)yl]-(thiono)-phosphoric(phosphonic) acid esters
US3706820A (en)	1972-12-19	S-alkylmercaptomethylthiophosphoric or phosphonic acid esters
US3966920A (en)	1976-06-29	O,S-Dialkyl-O-(2-cyanophenyl)-thionothiolphosphoric acid esters and insecticidal and acaricidal compositions and method
IL34314A (en)	1972-12-29	O-alkyl(or cycloalkyl)-s-(n,n-dialkylaminocarbamylmethyl)esters of alkyl-and aryl-thiolphosphonic and-thionothiolphosphonic acids,their preparation and use as insecticides and acaricides
US4002744A (en)	1977-01-11	O-Ethyl-O-iso-butyl-O-(2,2-dichlorovinyl)-thiono-phosphoric acid ester
IL32650A (en)	1972-12-29	Thionophosphonic acid esters,their preparation and use for combatting insects
US4000268A (en)	1976-12-28	N,N-dimethyl-N'-[O-phenyl-(thiono)-alkane-phosphonyl]-formamidines
US3752871A (en)	1973-08-14	O - alkyl - n-monoalkyl-s-(n'-acyl-carbamylmethyl) - thionothiolphosphoric acid ester amides
IL38701A (en)	1974-12-31	Substituted pyrazol(3)yl-carbamic acid esters,their preparation and their use as insecticides or acaricides
US3940457A (en)	1976-02-24	N-(N,N-disubstituted-aminomethylidene)-(thiono)thiol-phosphoric acid esters amides
IL33731A (en)	1972-11-28	O,o-dialkyl-s-(1,2,2-trichloroethyl)-thionothiolphosphoric acid esters and o-alkyl-s-(1,2,2-trichloroethyl)-alkane-thionothiolphosphonic acid esters,their preparation and use as insecticides
IL47240A (en)	1977-11-30	O-triazolyl-(thiono)-phosphoric(phosphonic phosphinic) acid esters and ester-amides their preparation and their use as insecticides acaricides or nematicides
US3733378A (en)	1973-05-15	Amido-o-lower alkyl-s-allylmercapto-methylthiolphosphoric acid esters
IL41933A (en)	1977-10-31	Disubstituted n-(aminomethylene)-thiolphosphoric and thiono-phosphoric acid ester amides their production and their use as insecticides and acaricides
US3957979A (en)	1976-05-18	Pesticidal N-(O-S-dialkyl(thionol)-thiolPhosphoryl)-iminoformic acid alkyl esters