DK141202B - Thiadiazolylimidazolidinoner med herbicid virkning. - Google Patents

Thiadiazolylimidazolidinoner med herbicid virkning. Download PDF

Info

Publication number: DK141202B
Authority: DK; Denmark
Prior art keywords: ooo; approx; thiadiazol; compounds; thiadiazolylimidazolidinones
Prior art date: 1973-06-29

Application number

DK258074AA

Other languages

Danish (da)

English (en)

Other versions

DK141202C (de

DK258074A (de

Inventor

John Krenzer

Original Assignee

Velsicol Chemical Corp

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.)

1973-06-29

Filing date

1974-05-09

Publication date

1980-02-04

1974-05-09 Application filed by Velsicol Chemical Corp filed Critical Velsicol Chemical Corp

1975-02-17 Publication of DK258074A publication Critical patent/DK258074A/da

1980-02-04 Publication of DK141202B publication Critical patent/DK141202B/da

1980-07-21 Application granted granted Critical

1980-07-21 Publication of DK141202C publication Critical patent/DK141202C/da

Links

230000002363 herbicidal effect Effects 0.000 title description 16
150000001875 compounds Chemical class 0.000 description 32
241000196324 Embryophyta Species 0.000 description 30
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 24
239000000203 mixture Substances 0.000 description 23
239000000047 product Substances 0.000 description 20
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
239000011541 reaction mixture Substances 0.000 description 15
238000010992 reflux Methods 0.000 description 13
SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 12
238000002360 preparation method Methods 0.000 description 11
-1 hydrochloric acid Chemical class 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
239000000843 powder Substances 0.000 description 8
239000002244 precipitate Substances 0.000 description 8
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 7
239000011521 glass Substances 0.000 description 7
239000002689 soil Substances 0.000 description 7
239000000243 solution Substances 0.000 description 7
238000002474 experimental method Methods 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
239000007787 solid Substances 0.000 description 6
239000000539 dimer Substances 0.000 description 5
238000000034 method Methods 0.000 description 5
238000005507 spraying Methods 0.000 description 5
108010093488 His-His-His-His-His-His Proteins 0.000 description 4
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-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
229910001873 dinitrogen Inorganic materials 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
239000000706 filtrate Substances 0.000 description 3
238000001914 filtration Methods 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000004009 herbicide Substances 0.000 description 3
239000012948 isocyanate Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000012429 reaction media Substances 0.000 description 3
239000012047 saturated solution Substances 0.000 description 3
239000002002 slurry Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
KZMQZFPRPILIHO-UHFFFAOYSA-N 2-(methylamino)acetaldehyde Chemical compound CNCC=O KZMQZFPRPILIHO-UHFFFAOYSA-N 0.000 description 2
TWAUUVMXSRYMPA-UHFFFAOYSA-N 2-tert-butyl-5-isocyanato-1,3,4-thiadiazole Chemical class CC(C)(C)C1=NN=C(N=C=O)S1 TWAUUVMXSRYMPA-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 2
241000209117 Panicum Species 0.000 description 2
235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 2
235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
239000000443 aerosol Substances 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000004821 distillation Methods 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
239000008187 granular material Substances 0.000 description 2
238000000227 grinding Methods 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
210000001699 lower leg Anatomy 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000002245 particle Substances 0.000 description 2
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical class O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 2
238000009331 sowing Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
231100000331 toxic Toxicity 0.000 description 2
230000002588 toxic effect Effects 0.000 description 2
125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 description 1
WUCYDSVAAKJISH-UHFFFAOYSA-N 1-methyl-1-(2-oxoethyl)-3-(5-propan-2-yl-1,3,4-thiadiazol-2-yl)urea Chemical compound CN(C(=O)NC1=NN=C(S1)C(C)C)CC=O WUCYDSVAAKJISH-UHFFFAOYSA-N 0.000 description 1
AWFYPPSBLUWMFQ-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(1,4,6,7-tetrahydropyrazolo[4,3-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=C2 AWFYPPSBLUWMFQ-UHFFFAOYSA-N 0.000 description 1
LJGUQVJJWFWIBA-UHFFFAOYSA-N 2-isocyanato-5-(trifluoromethyl)-1,3,4-thiadiazole Chemical class FC(F)(F)C1=NN=C(N=C=O)S1 LJGUQVJJWFWIBA-UHFFFAOYSA-N 0.000 description 1
LTEUXHSAYOSFGQ-UHFFFAOYSA-N 5-(trifluoromethyl)-1,3,4-thiadiazol-2-amine Chemical compound NC1=NN=C(C(F)(F)F)S1 LTEUXHSAYOSFGQ-UHFFFAOYSA-N 0.000 description 1
ICXDPEFCLDSXLI-UHFFFAOYSA-N 5-tert-butyl-1,3,4-thiadiazol-2-amine Chemical compound CC(C)(C)C1=NN=C(N)S1 ICXDPEFCLDSXLI-UHFFFAOYSA-N 0.000 description 1
241000209761 Avena Species 0.000 description 1
235000007319 Avena orientalis Nutrition 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000012190 activator Substances 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
244000144972 livestock Species 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000003020 moisturizing effect Effects 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
239000012430 organic reaction media Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/135—Nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Plural Heterocyclic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
Cosmetics (AREA)
Medicines Containing Plant Substances (AREA)

DK258074AA 1973-06-29 1974-05-09 Thiadiazolylimidazolidinoner med herbicid virkning. DK141202B (da)

Applications Claiming Priority (6)

Application Number	Priority Date	Filing Date
US37520373A	1973-06-29	1973-06-29
US37520373		1973-06-29
US38341773A	1973-07-27	1973-07-27
US38341773		1973-07-27
US38800573A	1973-08-13	1973-08-13
US38800573		1973-08-13

Publications (3)

Publication Number	Publication Date
DK258074A DK258074A (de)	1975-02-17
DK141202B true DK141202B (da)	1980-02-04
DK141202C DK141202C (de)	1980-07-21

Family

ID=27409234

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK258074AA DK141202B (da)	1973-06-29	1974-05-09	Thiadiazolylimidazolidinoner med herbicid virkning.

Country Status (22)

Country	Link
AR (1)	AR216038A1 (de)
AT (1)	AT335449B (de)
AU (1)	AU473700B2 (de)
BE (1)	BE813958A (de)
BR (1)	BR7405280A (de)
CA (1)	CA1017747A (de)
CH (1)	CH589409A5 (de)
DE (1)	DE2430467C2 (de)
DK (1)	DK141202B (de)
EG (1)	EG11069A (de)
ES (1)	ES424486A1 (de)
FR (1)	FR2235127B1 (de)
GB (1)	GB1450289A (de)
IL (1)	IL44428A (de)
IT (1)	IT1049287B (de)
MY (1)	MY7900229A (de)
NL (1)	NL7405880A (de)
NO (1)	NO140382C (de)
PH (1)	PH10348A (de)
SE (1)	SE401922B (de)
SU (1)	SU554814A3 (de)
YU (1)	YU36520B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1150271A (en) *	1979-08-10	1983-07-19	Jerome M. Lavanish	3-¬5-¬1-(alkyloxy or alkylthio)alkyl, alkynyl, alkenyl, or haloalkyl\|-1,3,4- thiadiazol-2-yl\|-4-hydroxy-1-methyl-2- imidazolidinones
AU581763B2 (en) *	1985-06-14	1989-03-02	Ppg Industries, Inc.	Herbicidal imidazolidinone derivatives
GB201419829D0 (en) *	2014-11-07	2014-12-24	Syngenta Participations Ag	Herbicidal compounds

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2013418A1 (de) *	1970-03-20	1971-10-07		I (1,3,4 Thiadiazol 2 yl) lmidazohdi non (2) Derivate, Verfahren zu ihrer Her stellung und ihre Verwendung als herbizide
DE2013406A1 (de) *	1970-03-20	1971-10-07		1(13 4 Thiadiazol 2 yl) lmidazohdi non (2) Derivate, Verfahren zu ihrer Her stellung und ihre Verwendung als herbizide

1974
- 1974-02-08 AR AR252264A patent/AR216038A1/es active
- 1974-03-15 IL IL44428A patent/IL44428A/en unknown
- 1974-03-19 CA CA195,374A patent/CA1017747A/en not_active Expired
- 1974-03-21 ES ES424486A patent/ES424486A1/es not_active Expired
- 1974-03-26 PH PH15660*A patent/PH10348A/en unknown
- 1974-03-29 YU YU00885/74A patent/YU36520B/xx unknown
- 1974-04-19 BE BE143416A patent/BE813958A/xx not_active IP Right Cessation
- 1974-04-30 NO NO741560A patent/NO140382C/no unknown
- 1974-05-02 NL NL7405880A patent/NL7405880A/xx not_active Application Discontinuation
- 1974-05-06 CH CH613574A patent/CH589409A5/xx not_active IP Right Cessation
- 1974-05-09 DK DK258074AA patent/DK141202B/da not_active IP Right Cessation
- 1974-05-13 SE SE7406371A patent/SE401922B/xx unknown
- 1974-05-29 IT IT51279/74A patent/IT1049287B/it active
- 1974-06-18 AU AU70162/74A patent/AU473700B2/en not_active Expired
- 1974-06-19 EG EG232/74A patent/EG11069A/xx active
- 1974-06-25 DE DE2430467A patent/DE2430467C2/de not_active Expired
- 1974-06-25 FR FR7422142A patent/FR2235127B1/fr not_active Expired
- 1974-06-27 BR BR5280/74A patent/BR7405280A/pt unknown
- 1974-06-28 AT AT538074A patent/AT335449B/de not_active IP Right Cessation
- 1974-06-28 SU SU2049687A patent/SU554814A3/ru active
- 1974-06-28 GB GB2871674A patent/GB1450289A/en not_active Expired
1979
- 1979-12-30 MY MY229/79A patent/MY7900229A/xx unknown

Also Published As

Publication number	Publication date
AU7016274A (en)	1975-12-18
DK141202C (de)	1980-07-21
GB1450289A (en)	1976-09-22
NO741560L (de)	1975-01-27
DE2430467C2 (de)	1983-07-21
PH10348A (en)	1976-12-20
AT335449B (de)	1977-03-10
AU473700B2 (en)	1976-07-01
CH589409A5 (de)	1977-07-15
FR2235127A1 (de)	1975-01-24
ATA538074A (de)	1976-07-15
AR216038A1 (es)	1979-11-30
NO140382B (no)	1979-05-14
BR7405280D0 (pt)	1975-01-21
ES424486A1 (es)	1976-06-01
NO140382C (no)	1979-08-22
YU88574A (en)	1982-02-25
BR7405280A (pt)	1976-02-24
SE401922B (sv)	1978-06-05
IL44428A0 (en)	1974-06-30
NL7405880A (de)	1974-12-31
BE813958A (fr)	1974-08-16
EG11069A (en)	1976-11-30
DK258074A (de)	1975-02-17
FR2235127B1 (de)	1980-02-08
SU554814A3 (ru)	1977-04-15
DE2430467A1 (de)	1975-01-23
YU36520B (en)	1984-02-29
SE7406371L (de)	1974-12-30
IL44428A (en)	1977-08-31
IT1049287B (it)	1981-01-20
MY7900229A (en)	1979-12-31
CA1017747A (en)	1977-09-20

Legal Events

Date	Code	Title	Description
1987-01-26	PBP	Patent lapsed

Publication	Publication Date	Title
AU600434B2 (en)	1990-08-16	Use of quinoline derivatives for the protection of cultivated plants
PL144046B1 (en)	1988-04-30	Process for preparing novel 2-/2-substituted-benzoyl/-cyclohexanodiones-1,3 and herbicide
JPH059432B2 (de)	1993-02-04
NO162663B (no)	1989-10-23	Nye 2-(2'-nitrobenzoyl)-1,2-cykloheksandioner, herbicide preparater inneholdende disse og fremgangsmaate for deres fremstilling.
RS49899B (sr)	2008-08-07	Derivati 4-benzoilizoksazola, postupak za njihovo dobijanje, herbicidni preparati koji ih sadrže i njihova primena za kontrolu rasta korova
PL149280B1 (en)	1990-01-31	Process for preparing novel 2-/2-substituted-benzoyl/-cyclohexanodi-1,3-ones and herbicide
HRP920255A2 (en)	1995-08-31	Herbicides
KR870001088B1 (ko)	1987-06-04	2-[1-(옥시아미노)-알킬리덴]사이클로핵산-1,3-디온 유도체의 제조방법
KR910001130B1 (ko)	1991-02-25	벤조트리아졸의 제조방법
JP2004002324A (ja)	2004-01-08	除草剤組成物
US3454392A (en)	1969-07-08	Dihalophenyl-p-nitrophenyl ethers as herbicides
JPH0331266A (ja)	1991-02-12	ピリミジン誘導体及び除草剤
CA1075697A (en)	1980-04-15	3-phenyl-5-substituted-4(1h)-pyridones(thiones)
DK141202B (da)	1980-02-04	Thiadiazolylimidazolidinoner med herbicid virkning.
KR920001468B1 (ko)	1992-02-14	2-페닐-4,5,6,7-테트라히드로-2h-인다졸류의 제조방법
US4290798A (en)	1981-09-22	Herbicidal compound and method of use
RU1811362C (ru)	1993-04-23	Производные 1,5-дифенил-1,2,4-триазол-3-карбоновой кислоты, обладающие антидотной активностью и гербицидно-антидотна композици
US3932458A (en)	1976-01-13	Antimicrobial and plant-active 4,5-dihalopyrrole-2-carbonitriles
JPH0130818B2 (de)	1989-06-22
EP0064353B1 (de)	1986-05-21	Verwendung von 2,4-disubstituierten 5-Thiazolcarbonsäuren und deren Derivaten, um die von Acetamidherbiziden verursachten Saatpflanzenschäden zu vermindern
US3985539A (en)	1976-10-12	4,5-Dihalopyrrole-2-carbonitrile-containing terrestrial and aquatic hebicidal composition
JPH0339501B2 (de)	1991-06-14
KR840000699B1 (ko)	1984-05-21	1-알킬-3-페닐피리디늄 염의 제조방법
GB2103610A (en)	1983-02-23	Herbicidal compounds derived from N-sulphonyl-aryloxybenamides and the processes for their preparation and use
CS242891B2 (en)	1986-05-15	Herbicide