JPS637534B2 - - Google Patents

Info

Publication number: JPS637534B2
Authority: JP; Japan
Prior art keywords: hydrogen; chlorine; compound according; iodine; bromine
Prior art date: 1982-03-25
Legal status (The legal status 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 status listed.): Expired

Application number

JP4807383A

Other languages

English (en)

Japanese (ja)

Other versions

JPS58180451A (ja

Inventor

Jeemusu Michaerii Uiriamu

Uein Kuraatsu Gaarii

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Stauffer Chemical Co

Original Assignee

Stauffer Chemical Co

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.)

1982-03-25

Filing date

1983-03-24

Publication date

1988-02-17

1983-03-24 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1983-10-21 Publication of JPS58180451A publication Critical patent/JPS58180451A/ja

1988-02-17 Publication of JPS637534B2 publication Critical patent/JPS637534B2/ja

Status Granted legal-status Critical Current

Links

229910052739 hydrogen Inorganic materials 0.000 claims description 62
239000001257 hydrogen Substances 0.000 claims description 62
229910052801 chlorine Inorganic materials 0.000 claims description 52
239000000460 chlorine Substances 0.000 claims description 52
150000001875 compounds Chemical class 0.000 claims description 39
150000002431 hydrogen Chemical class 0.000 claims description 39
238000000034 method Methods 0.000 claims description 23
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 21
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 14
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 11
229910052740 iodine Inorganic materials 0.000 claims description 11
239000011630 iodine Substances 0.000 claims description 11
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 10
229910052794 bromium Inorganic materials 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
125000001424 substituent group Chemical group 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
230000001629 suppression Effects 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims 1
239000000203 mixture Substances 0.000 description 24
230000002363 herbicidal effect Effects 0.000 description 17
241000196324 Embryophyta Species 0.000 description 15
239000000843 powder Substances 0.000 description 14
239000002689 soil Substances 0.000 description 12
239000004480 active ingredient Substances 0.000 description 11
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
239000004009 herbicide Substances 0.000 description 8
239000007788 liquid Substances 0.000 description 8
238000009472 formulation Methods 0.000 description 7
238000012360 testing method Methods 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
231100000614 poison Toxicity 0.000 description 6
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
-1 2-(2-substituted benzoyl)-cyclohexane-1,3-dione Chemical class 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 5
239000004927 clay Substances 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
239000000243 solution Substances 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000002270 dispersing agent Substances 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
239000007921 spray Substances 0.000 description 4
240000006995 Abutilon theophrasti Species 0.000 description 3
241000209764 Avena fatua Species 0.000 description 3
235000007320 Avena fatua Nutrition 0.000 description 3
244000058871 Echinochloa crus-galli Species 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000002612 dispersion medium Substances 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
239000002574 poison Substances 0.000 description 3
230000007096 poisonous effect Effects 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
239000011592 zinc chloride Substances 0.000 description 3
235000005074 zinc chloride Nutrition 0.000 description 3
235000004535 Avena sterilis Nutrition 0.000 description 2
244000178993 Brassica juncea Species 0.000 description 2
235000005853 Cyperus esculentus Nutrition 0.000 description 2
240000001505 Cyperus odoratus Species 0.000 description 2
235000003403 Limnocharis flava Nutrition 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
235000015225 Panicum colonum Nutrition 0.000 description 2
240000003461 Setaria viridis Species 0.000 description 2
235000002248 Setaria viridis Nutrition 0.000 description 2
239000000654 additive Substances 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
150000001448 anilines Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
GJQBHOAJJGIPRH-UHFFFAOYSA-N benzoyl cyanide Chemical class N#CC(=O)C1=CC=CC=C1 GJQBHOAJJGIPRH-UHFFFAOYSA-N 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000012043 crude product Substances 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
230000035784 germination Effects 0.000 description 2
239000008187 granular material Substances 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
229930000184 phytotoxin Natural products 0.000 description 2
239000003123 plant toxin Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000004576 sand Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
238000009333 weeding Methods 0.000 description 2
239000008096 xylene Substances 0.000 description 2
SMYMJHWAQXWPDB-UHFFFAOYSA-N (2,4,5-trichlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl SMYMJHWAQXWPDB-UHFFFAOYSA-N 0.000 description 1
239000003559 2,4,5-trichlorophenoxyacetic acid Substances 0.000 description 1
MJJCNUBDKYFMHM-UHFFFAOYSA-N 2,4-dichlorobenzoyl cyanide Chemical compound ClC1=CC=C(C(=O)C#N)C(Cl)=C1 MJJCNUBDKYFMHM-UHFFFAOYSA-N 0.000 description 1
OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-N 0.000 description 1
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
FBMDQVBGIYSDTI-UHFFFAOYSA-N 2-n,4-n-bis(3-methoxypropyl)-6-methylsulfanyl-1,3,5-triazine-2,4-diamine Chemical compound COCCCNC1=NC(NCCCOC)=NC(SC)=N1 FBMDQVBGIYSDTI-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
NAOCHJCREOAPOF-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-1,1-dimethylurea Chemical compound CN(C)C(=O)NC1=CC(Cl)=CC(Cl)=C1 NAOCHJCREOAPOF-UHFFFAOYSA-N 0.000 description 1
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
240000001592 Amaranthus caudatus Species 0.000 description 1
235000009328 Amaranthus caudatus Nutrition 0.000 description 1
241000219198 Brassica Species 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
235000011332 Brassica juncea Nutrition 0.000 description 1
235000014698 Brassica juncea var multisecta Nutrition 0.000 description 1
235000014700 Brassica juncea var napiformis Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
JGLMVXWAHNTPRF-CMDGGOBGSA-N CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O Chemical compound CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O JGLMVXWAHNTPRF-CMDGGOBGSA-N 0.000 description 1
HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 1
240000001549 Ipomoea eriocarpa Species 0.000 description 1
235000005146 Ipomoea eriocarpa Nutrition 0.000 description 1
239000005574 MCPA Substances 0.000 description 1
PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 1
235000010086 Setaria viridis var. viridis Nutrition 0.000 description 1
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
150000003869 acetamides Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
125000000304 alkynyl group Chemical group 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
UGFSSCKCYPZCAO-UHFFFAOYSA-N azepane-1-carbothioic s-acid Chemical compound SC(=O)N1CCCCCC1 UGFSSCKCYPZCAO-UHFFFAOYSA-N 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical class [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000011362 coarse particle Substances 0.000 description 1
239000002361 compost Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
230000001276 controlling effect Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
150000001879 copper Chemical class 0.000 description 1
OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
235000019425 dextrin Nutrition 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000284 extract Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
238000007429 general method Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000003292 glue Substances 0.000 description 1
239000003864 humus Substances 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
239000011147 inorganic material Substances 0.000 description 1
229910003480 inorganic solid Inorganic materials 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
239000003621 irrigation water 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
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000002362 mulch Substances 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
239000010451 perlite Substances 0.000 description 1
235000019362 perlite Nutrition 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003209 petroleum derivative Substances 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
238000012545 processing Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
YRNIQASZWVFCJP-UHFFFAOYSA-N s-ethyl carbamothioate Chemical class CCSC(N)=O YRNIQASZWVFCJP-UHFFFAOYSA-N 0.000 description 1
238000012216 screening Methods 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
230000007226 seed germination Effects 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
229940035044 sorbitan monolaurate Drugs 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000003419 tautomerization reaction Methods 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
231100000167 toxic agent Toxicity 0.000 description 1
239000003440 toxic substance Substances 0.000 description 1
238000012546 transfer Methods 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000005303 weighing Methods 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP4807383A 1982-03-25 1983-03-24 ２−（２−置換ベンゾイル）−１，３−シクロヘキサンジオン類 Granted JPS58180451A (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date
US36165882A	1982-03-25	1982-03-25
US361658		1982-03-25
US464251		1983-02-09

Publications (2)

Publication Number	Publication Date
JPS58180451A JPS58180451A (ja)	1983-10-21
JPS637534B2 true JPS637534B2 (de)	1988-02-17

Family

ID=23422955

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP4807383A Granted JPS58180451A (ja)	1982-03-25	1983-03-24	２−（２−置換ベンゾイル）−１，３−シクロヘキサンジオン類

Country Status (3)

Country	Link
JP (1)	JPS58180451A (de)
HU (1)	HU191288B (de)
ZA (1)	ZA832094B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4938796A (en) *	1987-07-06	1990-07-03	Ici Americas Inc.	Herbicidal compositions of acylated 1,3-dicarbonyl herbicides and antidotes therefor
AUPR484201A0 (en) *	2001-05-08	2001-05-31	Bioprospect Limited	Pesticidal compositions
CN105766944B (zh) *	2014-12-22	2018-12-14	沈阳中化农药化工研发有限公司	一种除草剂及其应用

1983
- 1983-03-24 JP JP4807383A patent/JPS58180451A/ja active Granted
- 1983-03-24 ZA ZA832094A patent/ZA832094B/xx unknown
- 1983-03-24 HU HU99883A patent/HU191288B/hu not_active IP Right Cessation

Also Published As

Publication number	Publication date
JPS58180451A (ja)	1983-10-21
ZA832094B (en)	1984-03-28
HU191288B (en)	1987-02-27

Publication	Publication Date	Title
EP0090262B1 (de)	1992-08-05	2-(2-Substituierte Benzoyl)-1,3 cyclohexandione
EP0137963B1 (de)	1988-09-28	Bestimmte 2-(2-substituierte Benzoyl)-1,3-cyclohexandione
KR890000193B1 (ko)	1989-03-10	2-(2-치환 벤조일)-1, 3-시클로헥산디온
US4681621A (en)	1987-07-21	Herbicidal 2-(2-substituted benzoyl)-1,3-cyclopentanediones
US4083867A (en)	1978-04-11	N-dimethylpropynyl-α-methoxy-α-(3,5-dimethylphenoxy)acetamide and its use as herbicides
EP0162336B1 (de)	1989-03-22	Bestimmte 2-[2-(substituierte Phenyl)acetyl]-1,3-cyclohexandione
US4482727A (en)	1984-11-13	Certain 1,3-cyclohexanedione adducts of substituted phenoxyphenoxypropionic acids and their use as an herbicide
US4052432A (en)	1977-10-04	N-(1,1 Substituted acetonitrilo)-α-(3,5-substituted phenoxy) alkyl amides
JPH0130818B2 (de)	1989-06-22
US4050923A (en)	1977-09-27	N-benzyl-2-(3,5-dimethyl phenoxy)-2-alkoxy amide herbicides
JPS637534B2 (de)	1988-02-17
EP0180787B1 (de)	1988-04-20	2-Bromo-4-methylimidazol-5-carbonsäureester
US3953507A (en)	1976-04-27	N-t-butyl-α-(3,5-substituted phenoxy) alkyl amides and their use as herbicides
US4049424A (en)	1977-09-20	N-t-butyl-2-(3,5-dichloro or dimethyl phenoxy)-2-alkoxy amide herbicides
US4082800A (en)	1978-04-04	N-t-butyl-2-(3,5-dichloro or dimethyl phenoxy)-2-alkoxy amides and their use as herbicides
US4170463A (en)	1979-10-09	2,6-Dialkyl-N-dialkylphosphonomethyl chloroacetanilides as herbicides
US4087277A (en)	1978-05-02	N-(1,1-substituted acetonitrilo)-α-(3,5-substituted phenoxy) alkyl amides and their use as herbicides
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