JPH0247464B2 - - Google Patents

Info

Publication number: JPH0247464B2
Authority: JP; Japan
Prior art keywords: carbon atoms; compound; group; chloro; weight
Prior art date: 1981-09-01
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 - Lifetime

Application number

JP56138044A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5838256A (ja

Inventor

Hideyoshi Nagano

Shunichi Hashimoto

Akira Yoshida

Keiji Matsumoto

Katsuzo Kamoshita

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.)

Sumitomo Chemical Co Ltd

Original Assignee

Sumitomo Chemical Co Ltd

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.)

1981-09-01

Filing date

1981-09-01

Publication date

1990-10-19

1981-09-01 Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd

1981-09-01 Priority to JP13804481A priority Critical patent/JPS5838256A/ja

1982-03-23 Priority to US06/360,997 priority patent/US4484940A/en

1982-03-23 Priority to US06/360,999 priority patent/US4484941A/en

1982-03-25 Priority to AU81930/82A priority patent/AU550845B2/en

1982-03-26 Priority to DK140382A priority patent/DK154212C/da

1982-03-26 Priority to EP82102565A priority patent/EP0061741B1/en

1982-03-26 Priority to DE8282102565T priority patent/DE3266288D1/de

1982-03-29 Priority to HU95382A priority patent/HU187451B/hu

1982-03-29 Priority to ES510917A priority patent/ES510917A0/es

1982-03-29 Priority to KR8201345A priority patent/KR890000766B1/ko

1982-03-29 Priority to CA000399608A priority patent/CA1164467A/en

1982-03-29 Priority to AR28891182A priority patent/AR230424A1/es

1982-03-29 Priority to SU823415050A priority patent/SU1611206A3/ru

1982-03-29 Priority to CA000399595A priority patent/CA1164002A/en

1982-03-30 Priority to BG056020A priority patent/BG40644A3/xx

1982-03-30 Priority to BR8201807A priority patent/BR8201807A/pt

1982-03-30 Priority to MX793482A priority patent/MX155119A/es

1982-03-30 Priority to PL23570882A priority patent/PL133782B1/pl

1983-03-05 Publication of JPS5838256A publication Critical patent/JPS5838256A/ja

1983-05-24 Priority to CA000428781A priority patent/CA1186337A/en

1983-05-30 Priority to CA000429249A priority patent/CA1186338A/en

1984-09-18 Priority to US06/651,877 priority patent/US5030760A/en

1986-09-03 Priority to US06/903,830 priority patent/US4736068A/en

1987-02-10 Priority to MX922587A priority patent/MX9225A/es

1987-11-11 Priority to DK591387A priority patent/DK159845C/da

1987-12-09 Priority to US07/130,522 priority patent/US4835324A/en

1988-12-30 Priority to MY8800096A priority patent/MY8800096A/xx

1990-06-11 Priority to DK143090A priority patent/DK160487C/da

1990-06-11 Priority to DK142990A priority patent/DK163818C/da

1990-10-19 Publication of JPH0247464B2 publication Critical patent/JPH0247464B2/ja

1991-02-05 Priority to US07/650,943 priority patent/US5191105A/en

Status Granted legal-status Critical Current

Links

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239000004009 herbicide Substances 0.000 claims description 18
125000004432 carbon atom Chemical group C* 0.000 claims description 12
240000008042 Zea mays Species 0.000 claims description 9
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 9
235000002017 Zea mays subsp mays Nutrition 0.000 claims description 9
235000005822 corn Nutrition 0.000 claims description 9
CCFNMXDJVOYPEY-UHFFFAOYSA-N 2-phenyl-3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical class O=C1C2CCC=CC2C(=O)N1C1=CC=CC=C1 CCFNMXDJVOYPEY-UHFFFAOYSA-N 0.000 claims description 5
239000004480 active ingredient Substances 0.000 claims description 5
125000003342 alkenyl group Chemical group 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
125000000304 alkynyl group Chemical group 0.000 claims description 4
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BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
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244000058871 Echinochloa crus-galli Species 0.000 description 3
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240000001549 Ipomoea eriocarpa Species 0.000 description 3
235000005146 Ipomoea eriocarpa Nutrition 0.000 description 3
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235000011684 Sorghum saccharatum Nutrition 0.000 description 3
244000062793 Sorghum vulgare Species 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000004927 clay Substances 0.000 description 3
235000019441 ethanol Nutrition 0.000 description 3
239000008187 granular material Substances 0.000 description 3
239000002994 raw material Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
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QAWLSTWQUFLACC-UHFFFAOYSA-N 2-(4-chloro-2-fluoro-5-prop-2-ynoxyphenyl)-4,5,6,7-tetrahydroisoindole-1,3-dione Chemical compound FC1=CC(Cl)=C(OCC#C)C=C1N1C(=O)C(CCCC2)=C2C1=O QAWLSTWQUFLACC-UHFFFAOYSA-N 0.000 description 2
MFUPLJQNEXUUDW-UHFFFAOYSA-N 2-phenylisoindole-1,3-dione Chemical class O=C1C2=CC=CC=C2C(=O)N1C1=CC=CC=C1 MFUPLJQNEXUUDW-UHFFFAOYSA-N 0.000 description 2
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
240000001592 Amaranthus caudatus Species 0.000 description 2
235000009328 Amaranthus caudatus Nutrition 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
240000008955 Dioscorea japonica Species 0.000 description 2
235000005251 Dioscorea japonica Nutrition 0.000 description 2
235000008247 Echinochloa frumentacea Nutrition 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
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229920001732 Lignosulfonate Polymers 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
231100000674 Phytotoxicity Toxicity 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
229920002472 Starch Polymers 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 description 2
150000001346 alkyl aryl ethers Chemical class 0.000 description 2
239000000440 bentonite Substances 0.000 description 2
229910000278 bentonite Inorganic materials 0.000 description 2
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
239000000969 carrier Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
230000000887 hydrating effect Effects 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
238000002156 mixing Methods 0.000 description 2
NVGOPFQZYCNLDU-UHFFFAOYSA-N norflurazon Chemical compound O=C1C(Cl)=C(NC)C=NN1C1=CC=CC(C(F)(F)F)=C1 NVGOPFQZYCNLDU-UHFFFAOYSA-N 0.000 description 2
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238000012545 processing Methods 0.000 description 2
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239000004094 surface-active agent Substances 0.000 description 2
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239000004563 wettable powder Substances 0.000 description 2
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RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
FLTFAXYVWNGCHY-UHFFFAOYSA-N 1-[(6,6-dimethylcyclohexa-2,4-dien-1-yl)methyl]-3-(4-methylphenyl)urea Chemical compound C1=CC(C)=CC=C1NC(=O)NCC1C(C)(C)C=CC=C1 FLTFAXYVWNGCHY-UHFFFAOYSA-N 0.000 description 1
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150000008052 alkyl sulfonates Chemical class 0.000 description 1
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235000012211 aluminium silicate Nutrition 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000003931 anilides Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
229910052586 apatite Inorganic materials 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 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
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
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125000002091 cationic group Chemical group 0.000 description 1
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MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
CWJSHJJYOPWUGX-UHFFFAOYSA-N chlorpropham Chemical compound CC(C)OC(=O)NC1=CC=CC(Cl)=C1 CWJSHJJYOPWUGX-UHFFFAOYSA-N 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
UHJMECPUUCQFRL-UHFFFAOYSA-N ethyl 2-(2,6-diethylanilino)acetate Chemical compound CCOC(=O)CNC1=C(CC)C=CC=C1CC UHJMECPUUCQFRL-UHFFFAOYSA-N 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
OXHDYFKENBXUEM-UHFFFAOYSA-N glyphosine Chemical compound OC(=O)CN(CP(O)(O)=O)CP(O)(O)=O OXHDYFKENBXUEM-UHFFFAOYSA-N 0.000 description 1
238000000227 grinding Methods 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 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
238000004898 kneading Methods 0.000 description 1
ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000011707 mineral Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
VSIIXMUUUJUKCM-UHFFFAOYSA-D pentacalcium;fluoride;triphosphate Chemical compound [F-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O VSIIXMUUUJUKCM-UHFFFAOYSA-D 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000000825 pharmaceutical preparation Substances 0.000 description 1
229940127557 pharmaceutical product Drugs 0.000 description 1
239000013459 phenoxy herbicide Substances 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
239000003880 polar aprotic solvent Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
YORCIIVHUBAYBQ-UHFFFAOYSA-N propargyl bromide Chemical compound BrCC#C YORCIIVHUBAYBQ-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000010898 silica gel chromatography Methods 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
229940005550 sodium alginate Drugs 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000007787 solid Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
229940035893 uracil Drugs 0.000 description 1
235000013311 vegetables Nutrition 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
239000001993 wax Substances 0.000 description 1
238000009333 weeding Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)
Indole Compounds (AREA)

JP13804481A 1981-03-30 1981-09-01 Ｎ―フェニルテトラヒドロフタルイミド誘導体、その製造法およびこれらを有効成分として含有する除草剤 Granted JPS5838256A (ja)

Priority Applications (29)

Application Number	Priority Date	Filing Date	Title
JP13804481A JPS5838256A (ja)	1981-09-01	1981-09-01	Ｎ―フェニルテトラヒドロフタルイミド誘導体、その製造法およびこれらを有効成分として含有する除草剤
US06/360,997 US4484940A (en)	1981-09-01	1982-03-23	Tetrahydrophthalimides, and their production and use as herbicides
US06/360,999 US4484941A (en)	1981-09-01	1982-03-23	Tetrahydrophthalimides, and their production and use as herbicides
AU81930/82A AU550845B2 (en)	1981-03-30	1982-03-25	Tetrahydrophthalimides and their starting compounds
DK140382A DK154212C (da)	1981-03-30	1982-03-26	Tetrahydrophthalimider, et herbicidt praeparat indeholdende disse samt deres anvendelse til ukrudtsbekaempelse
EP82102565A EP0061741B1 (en)	1981-03-30	1982-03-26	Tetrahydrophthalimides, and their production and use
DE8282102565T DE3266288D1 (en)	1981-03-30	1982-03-26	Tetrahydrophthalimides, and their production and use
HU95382A HU187451B (en)	1981-03-30	1982-03-29	Herbicide compositions containing tetrahydro-phtalimide derivatives as active agents, and process for producing the active agents
ES510917A ES510917A0 (es)	1981-03-30	1982-03-29	Un procedimiento para la preparacion de tetrahidroftalimidas.
KR8201345A KR890000766B1 (ko)	1981-03-30	1982-03-29	테트라히드로프탈이미드의 제조방법
CA000399608A CA1164467A (en)	1981-09-01	1982-03-29	Tetrahydrophthalimides, and their production and use
AR28891182A AR230424A1 (es)	1981-03-30	1982-03-29	Nuevos derivados de 2-fluor-4-cloro o bromo 5-hidroxi anilino nitrobenceno procedimiento para prepararlos;n-(2-fluor-halo-5-fenil)3,4,5,6-tetrahidroftalimidas obtenidas a partir de dichos derivados y procedimientos para su preparacion
SU823415050A SU1611206A3 (ru)	1981-03-30	1982-03-29	Способ борьбы с нежелательной растительностью
CA000399595A CA1164002A (en)	1981-09-01	1982-03-29	Tetrahydrophthalimides, and their production and use
PL23570882A PL133782B1 (en)	1981-03-30	1982-03-30	Herbicide and process for preparing n-/4-halo-2-fluoro-5-substituted phenyl/-3,4,5,6-tetrahydrophtalimide
BG056020A BG40644A3 (en)	1981-03-30	1982-03-30	Herbicide means and method for protection from weeds
BR8201807A BR8201807A (pt)	1981-03-30	1982-03-30	Composto compostos intermediarios para o mesmo processos para sua respectiva preparacao composicao herbicida processo para controlar ervas daninhas e uso de um composto
MX793482A MX155119A (es)	1981-03-30	1982-03-30	Procedimiento para la preparacion de n-(2-fluoro-4-halo-5-fenil-substituidos)-3,4,5,6-tetra-hidroftalimidas
CA000428781A CA1186337A (en)	1981-09-01	1983-05-24	Intermediates for producing tetrahydrophthalimides
CA000429249A CA1186338A (en)	1981-09-01	1983-05-30	Starting materials for producing tetrahydrophthalimides
US06/651,877 US5030760A (en)	1981-09-01	1984-09-18	Tetrahydrophthalimides, and their production and use
US06/903,830 US4736068A (en)	1981-09-01	1986-09-03	Tetrahydrophthalimides and their production and use as herbicides
MX922587A MX9225A (es)	1981-09-01	1987-02-10	Procedimiento para preparar n-(2-fluoro-4-halo-5-fenil substituidos)-3,4,5,6 tetrahidroftalimidas y compuesto obtenido.
DK591387A DK159845C (da)	1981-03-30	1987-11-11	1-amino-2-fluor-4-halogenbenzenderivater og en fremgangsmaade til fremstilling deraf
US07/130,522 US4835324A (en)	1981-09-01	1987-12-09	Tetrahydrophthalimides, and their production and use
MY8800096A MY8800096A (en)	1981-03-30	1988-12-30	Tetrahydro phthalimides and their production and use
DK143090A DK160487C (da)	1981-03-30	1990-06-11	N-(2-fluor-4-halogen-5-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimidforbindelser og en fremgangsmaade til fremstilling deraf
DK142990A DK163818C (da)	1981-03-30	1990-06-11	4-fluor-2-halogen-5-nitrophenoler og en fremgangsmaade til fremstilling deraf
US07/650,943 US5191105A (en)	1981-09-01	1991-02-05	Tetrahydrophthalimides, and their production and use as herbicides

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP13804481A JPS5838256A (ja)	1981-09-01	1981-09-01	Ｎ―フェニルテトラヒドロフタルイミド誘導体、その製造法およびこれらを有効成分として含有する除草剤

Publications (2)

Publication Number	Publication Date
JPS5838256A JPS5838256A (ja)	1983-03-05
JPH0247464B2 true JPH0247464B2 (xx)	1990-10-19

Family

ID=15212693

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP13804481A Granted JPS5838256A (ja)	1981-03-30	1981-09-01	Ｎ―フェニルテトラヒドロフタルイミド誘導体、その製造法およびこれらを有効成分として含有する除草剤

Country Status (2)

Country	Link
JP (1)	JPS5838256A (xx)
MX (1)	MX9225A (xx)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5373557A (en) *	1976-12-13	1978-06-30	Mitsubishi Chem Ind Ltd	3,4,5,6,-tetrahydrophthalimide and herbicide containing the same
JPS5419965A (en) *	1977-07-12	1979-02-15	Mitsubishi Chem Ind Ltd	Preparation of n-substituted phenyl-3,4,5,6-tetrahydro-phthalimide
JPS55139359A (en) *	1979-04-13	1980-10-31	Mitsubishi Chem Ind Ltd	Tetrahydrophthalimides, and herbicide containing compound as effective component
JPS55139305A (en) *	1979-04-13	1980-10-31	Mitsubishi Chem Ind Ltd	Herbicide

1981
- 1981-09-01 JP JP13804481A patent/JPS5838256A/ja active Granted
1987
- 1987-02-10 MX MX922587A patent/MX9225A/es unknown

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5373557A (en) *	1976-12-13	1978-06-30	Mitsubishi Chem Ind Ltd	3,4,5,6,-tetrahydrophthalimide and herbicide containing the same
JPS5419965A (en) *	1977-07-12	1979-02-15	Mitsubishi Chem Ind Ltd	Preparation of n-substituted phenyl-3,4,5,6-tetrahydro-phthalimide
JPS55139359A (en) *	1979-04-13	1980-10-31	Mitsubishi Chem Ind Ltd	Tetrahydrophthalimides, and herbicide containing compound as effective component
JPS55139305A (en) *	1979-04-13	1980-10-31	Mitsubishi Chem Ind Ltd	Herbicide

Also Published As

Publication number	Publication date
JPS5838256A (ja)	1983-03-05
MX9225A (es)	1993-09-01

Publication	Publication Date	Title
JP2913214B2 (ja)	1999-06-28	植物の生長を調節するための相乗作用組成物
JPH02233602A (ja)	1990-09-17	除草剤
JPH0247464B2 (xx)	1990-10-19
JPH045012B2 (xx)	1992-01-30
JPH0331706B2 (xx)	1991-05-08
JP2516384B2 (ja)	1996-07-24	ペンズアミド誘導体
JPH0240673B2 (xx)	1990-09-12
JPS5936896B2 (ja)	1984-09-06	α−アセチル桂皮酸エステル誘導体、その製造法および該化合物よりなる除草剤
JPS62267274A (ja)	1987-11-19	１，２，４−オキサジアゾ−ル誘導体
JPS6320428B2 (xx)	1988-04-27
JPH0372635B2 (xx)	1991-11-19
JPS6258359B2 (xx)	1987-12-05
JPS6232192B2 (xx)	1987-07-13
JPS6248673A (ja)	1987-03-03	ベンゾチアジン誘導体およびその製法
JP2634068B2 (ja)	1997-07-23	ベンズアミド誘導体
JPS6113704B2 (xx)	1986-04-15
JPS6131106B2 (xx)	1986-07-17
JPS6316389B2 (xx)	1988-04-08
JPS6055502B2 (ja)	1985-12-05	メタフエノキシ安息香酸アミド誘導体、その製造法およびそれらを有効成分とする除草剤
JPS6030307B2 (ja)	1985-07-16	置換フエニル尿素誘導体、その製造法および該化合物からなる除草剤
JPS6250444B2 (xx)	1987-10-24
JPS59175407A (ja)	1984-10-04	除草剤
JPH10231221A (ja)	1998-09-02	除草剤組成物
JPH0517910B2 (xx)	1993-03-10
JPH0247465B2 (xx)	1990-10-19