NL7906019A - Carbaminezuurfenylesters, werkwijze voor het bereiden daarvan alsmede herbiciden, die deze verbindingen bevatten. - Google Patents

Carbaminezuurfenylesters, werkwijze voor het bereiden daarvan alsmede herbiciden, die deze verbindingen bevatten. Download PDF

Info

Publication number: NL7906019A
Authority: NL; Netherlands
Prior art keywords: phenyl; ester; acid; carbanilic; cyanoethyl
Prior art date: 1978-10-12

Application number

NL7906019A

Other languages

English (en)

Dutch (nl)

Original Assignee

Schering 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.)

1978-10-12

Filing date

1979-08-06

Publication date

1980-04-15

1979-08-06 Application filed by Schering Ag filed Critical Schering Ag

1980-04-15 Publication of NL7906019A publication Critical patent/NL7906019A/nl

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-1 CARBAMIC ACID PHENYL ESTERS Chemical class 0.000 title claims description 81
150000001875 compounds Chemical class 0.000 title claims description 35
238000000034 method Methods 0.000 title claims description 11
239000004009 herbicide Substances 0.000 title claims description 10
KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 title description 2
150000002148 esters Chemical class 0.000 claims description 64
239000002253 acid Substances 0.000 claims description 19
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 15
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 11
230000002363 herbicidal effect Effects 0.000 claims description 9
125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims description 6
238000002360 preparation method Methods 0.000 claims description 6
AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
150000007530 organic bases Chemical class 0.000 claims description 4
BSCCSDNZEIHXOK-UHFFFAOYSA-N phenyl carbamate Chemical class NC(=O)OC1=CC=CC=C1 BSCCSDNZEIHXOK-UHFFFAOYSA-N 0.000 claims description 4
PZJFPNCBZDYKMJ-UHFFFAOYSA-N 2-cyanoethyl-(3-methylphenyl)carbamic acid Chemical compound C(#N)CCN(C(O)=O)C1=CC(=CC=C1)C PZJFPNCBZDYKMJ-UHFFFAOYSA-N 0.000 claims description 2
150000001447 alkali salts Chemical class 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
239000002585 base Substances 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
150000007529 inorganic bases Chemical class 0.000 claims description 2
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims description 2
PWXJULSLLONQHY-UHFFFAOYSA-N phenylcarbamic acid Chemical compound OC(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-N 0.000 claims 3
DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 claims 2
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 1
BRTXEENUBBKSBG-UHFFFAOYSA-N [3-(propanoylamino)phenyl] n-(2-bromoethyl)-n-phenylcarbamate Chemical compound CCC(=O)NC1=CC=CC(OC(=O)N(CCBr)C=2C=CC=CC=2)=C1 BRTXEENUBBKSBG-UHFFFAOYSA-N 0.000 claims 1
QIRBEJLUPCBQPI-UHFFFAOYSA-N [3-(propanoylamino)phenyl] n-(2-cyanoethyl)-n-phenylcarbamate Chemical compound CCC(=O)NC1=CC=CC(OC(=O)N(CCC#N)C=2C=CC=CC=2)=C1 QIRBEJLUPCBQPI-UHFFFAOYSA-N 0.000 claims 1
RRUKKXYUYBMUOJ-UHFFFAOYSA-N [3-(propanoylamino)phenyl] n-(2-ethoxyethyl)-n-phenylcarbamate Chemical compound C=1C=CC=CC=1N(CCOCC)C(=O)OC1=CC=CC(NC(=O)CC)=C1 RRUKKXYUYBMUOJ-UHFFFAOYSA-N 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
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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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WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
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XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
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239000008187 granular material Substances 0.000 description 2
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238000001228 spectrum Methods 0.000 description 2
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VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
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ONPGFTVBLFAILH-DUXPYHPUSA-N (e)-n-(3-hydroxyphenyl)but-2-enamide Chemical compound C\C=C\C(=O)NC1=CC=CC(O)=C1 ONPGFTVBLFAILH-DUXPYHPUSA-N 0.000 description 1
PYJOSHDBCVEHSA-UHFFFAOYSA-N 2,2-dimethoxyethyl(phenyl)carbamic acid Chemical compound COC(OC)CN(C(O)=O)C1=CC=CC=C1 PYJOSHDBCVEHSA-UHFFFAOYSA-N 0.000 description 1
NUBKYCCXDNYHLQ-UHFFFAOYSA-N 2,2-dimethylpentanoyl chloride Chemical compound CCCC(C)(C)C(Cl)=O NUBKYCCXDNYHLQ-UHFFFAOYSA-N 0.000 description 1
NVAYCFVXLGWWCD-UHFFFAOYSA-N 2-hydroxyethyl(phenyl)carbamic acid Chemical compound OCCN(C(O)=O)C1=CC=CC=C1 NVAYCFVXLGWWCD-UHFFFAOYSA-N 0.000 description 1
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YXSKGOCVSTWEJU-UHFFFAOYSA-N n-(3-hydroxyphenyl)propanamide Chemical compound CCC(=O)NC1=CC=CC(O)=C1 YXSKGOCVSTWEJU-UHFFFAOYSA-N 0.000 description 1
YTCACQVZWKHHJO-UHFFFAOYSA-N n-(cyanomethyl)-n-(3-methylphenyl)carbamoyl chloride Chemical compound CC1=CC=CC(N(CC#N)C(Cl)=O)=C1 YTCACQVZWKHHJO-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
231100001184 nonphytotoxic Toxicity 0.000 description 1
230000009965 odorless effect Effects 0.000 description 1
210000002741 palatine tonsil Anatomy 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000012071 phase Substances 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
235000009736 ragweed Nutrition 0.000 description 1
244000165825 ragweed Species 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 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
150000003560 thiocarbamic acids Chemical class 0.000 description 1
KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/28—Radicals substituted by nitrogen atoms
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
Plural Heterocyclic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

NL7906019A 1978-10-12 1979-08-06 Carbaminezuurfenylesters, werkwijze voor het bereiden daarvan alsmede herbiciden, die deze verbindingen bevatten. NL7906019A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19782844811 DE2844811A1 (de)	1978-10-12	1978-10-12	Carbaminsaeurephenylester, verfahren zur herstellung dieser verbindungen sowie diese enthaltendes herbizides mittel
DE2844811		1978-10-12

Publications (1)

Publication Number	Publication Date
NL7906019A true NL7906019A (nl)	1980-04-15

Family

ID=6052188

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL7906019A NL7906019A (nl)	1978-10-12	1979-08-06	Carbaminezuurfenylesters, werkwijze voor het bereiden daarvan alsmede herbiciden, die deze verbindingen bevatten.

Country Status (33)

Country	Link
JP (1)	JPS5817744B2 (fr)
AR (1)	AR223188A1 (fr)
AT (1)	AT368360B (fr)
AU (1)	AU522297B2 (fr)
BE (1)	BE879388A (fr)
BR (1)	BR7906612A (fr)
CA (1)	CA1124251A (fr)
CH (1)	CH641768A5 (fr)
CS (1)	CS208137B2 (fr)
DD (1)	DD146540A5 (fr)
DE (1)	DE2844811A1 (fr)
EG (1)	EG13844A (fr)
ES (1)	ES484478A1 (fr)
FI (1)	FI792941A7 (fr)
FR (1)	FR2438648A1 (fr)
GB (1)	GB2033383B (fr)
GR (1)	GR74033B (fr)
HU (1)	HU185779B (fr)
IL (1)	IL58420A (fr)
IN (1)	IN153182B (fr)
IT (1)	IT1162589B (fr)
MA (1)	MA18607A1 (fr)
MX (1)	MX5735E (fr)
NL (1)	NL7906019A (fr)
PH (1)	PH15549A (fr)
PL (1)	PL119533B1 (fr)
PT (1)	PT70232A (fr)
RO (1)	RO79322A (fr)
SE (1)	SE7908273L (fr)
SU (1)	SU1083906A3 (fr)
TR (1)	TR20602A (fr)
YU (1)	YU204979A (fr)
ZA (1)	ZA795472B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2844806A1 (de) *	1978-10-11	1980-04-24	Schering Ag	Carbanilsaeure- eckige klammer auf 3-(alkylcarbonylamino)-phenyl eckige klammer zu -ester, verfahren zur herstellung dieser verbindungen sowie diese enthaltendes herbizides mittel
EP0051564A1 (fr) *	1980-10-31	1982-05-12	Ciba-Geigy Ag	Carbamates
AU7645298A (en) *	1997-04-21	1998-11-13	Novartis Ag	Novel herbicides

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3865867A (en) *	1967-06-19	1975-02-11	Monsanto Co	Meta-bifunctional benzenes
CA975775A (en) *	1969-03-12	1975-10-07	Eugene G. Teach	Bromoacetanilides and their utility as biocides
FR2210186A5 (en) *	1972-12-13	1974-07-05	Rhone Progil	Halogenated ureidophenyl carbamates - herbicides, by reacting corresp. halophenols and isocyanates

1978
- 1978-10-12 DE DE19782844811 patent/DE2844811A1/de not_active Withdrawn
1979
- 1979-08-06 NL NL7906019A patent/NL7906019A/nl not_active Application Discontinuation
- 1979-08-21 YU YU02049/79A patent/YU204979A/xx unknown
- 1979-09-14 IN IN644/DEL/79A patent/IN153182B/en unknown
- 1979-09-21 FI FI792941A patent/FI792941A7/fi not_active Application Discontinuation
- 1979-09-26 ES ES484478A patent/ES484478A1/es not_active Expired
- 1979-09-26 PT PT70232A patent/PT70232A/pt unknown
- 1979-09-27 MX MX798406U patent/MX5735E/es unknown
- 1979-09-28 TR TR20602A patent/TR20602A/xx unknown
- 1979-10-01 GB GB7933946A patent/GB2033383B/en not_active Expired
- 1979-10-02 MA MA18807A patent/MA18607A1/fr unknown
- 1979-10-05 SE SE7908273A patent/SE7908273L/xx not_active Application Discontinuation
- 1979-10-08 DD DD79216084A patent/DD146540A5/de unknown
- 1979-10-09 IL IL58420A patent/IL58420A/xx unknown
- 1979-10-10 CH CH911579A patent/CH641768A5/de not_active IP Right Cessation
- 1979-10-10 EG EG593/79A patent/EG13844A/xx active
- 1979-10-10 PL PL1979218851A patent/PL119533B1/pl unknown
- 1979-10-10 GR GR60230A patent/GR74033B/el unknown
- 1979-10-11 CA CA337,402A patent/CA1124251A/fr not_active Expired
- 1979-10-11 AT AT0664579A patent/AT368360B/de not_active IP Right Cessation
- 1979-10-11 IT IT26401/79A patent/IT1162589B/it active
- 1979-10-11 SU SU792824354A patent/SU1083906A3/ru active
- 1979-10-11 HU HU79SCHE696A patent/HU185779B/hu unknown
- 1979-10-11 RO RO7998910A patent/RO79322A/fr unknown
- 1979-10-11 FR FR7925313A patent/FR2438648A1/fr active Granted
- 1979-10-11 BR BR7906612A patent/BR7906612A/pt unknown
- 1979-10-11 AU AU51684/79A patent/AU522297B2/en not_active Ceased
- 1979-10-12 JP JP54130948A patent/JPS5817744B2/ja not_active Expired
- 1979-10-12 AR AR278479A patent/AR223188A1/es active
- 1979-10-12 CS CS796953A patent/CS208137B2/cs unknown
- 1979-10-12 ZA ZA00795472A patent/ZA795472B/xx unknown
- 1979-10-12 PH PH23165A patent/PH15549A/en unknown
- 1979-10-12 BE BE0/197628A patent/BE879388A/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
AU522297B2 (en)	1982-05-27
IT1162589B (it)	1987-04-01
FI792941A7 (fi)	1981-01-01
PL119533B1 (en)	1982-01-30
GR74033B (fr)	1984-06-06
CA1124251A (fr)	1982-05-25
AU5168479A (en)	1980-04-17
SU1083906A3 (ru)	1984-03-30
MA18607A1 (fr)	1980-07-01
AR223188A1 (es)	1981-07-31
DD146540A5 (de)	1981-02-18
ZA795472B (en)	1980-09-24
PT70232A (de)	1979-10-01
FR2438648A1 (fr)	1980-05-09
FR2438648B1 (fr)	1983-09-16
YU204979A (en)	1983-04-30
ES484478A1 (es)	1980-05-16
DE2844811A1 (de)	1980-09-04
ATA664579A (de)	1982-02-15
IL58420A (en)	1984-05-31
HU185779B (en)	1985-03-28
JPS5559158A (en)	1980-05-02
BR7906612A (pt)	1980-06-17
JPS5817744B2 (ja)	1983-04-09
IT7926401A0 (it)	1979-10-11
IL58420A0 (en)	1980-01-31
IN153182B (fr)	1984-06-09
PL218851A1 (fr)	1980-07-28
CS208137B2 (en)	1981-08-31
EG13844A (en)	1982-09-30
BE879388A (fr)	1980-04-14
SE7908273L (sv)	1980-04-13
CH641768A5 (de)	1984-03-15
GB2033383A (en)	1980-05-21
AT368360B (de)	1982-10-11
PH15549A (en)	1983-02-09
MX5735E (es)	1984-01-25
RO79322A (fr)	1982-08-17
TR20602A (tr)	1982-01-01
GB2033383B (en)	1983-05-11

Legal Events

Date	Code	Title
1980-04-25	A1A	A request for search or an international-type search has been filed
1981-09-01	BB	A search report has been drawn up
1985-01-01	A85	Still pending on 85-01-01
1986-10-01	BV	The patent application has lapsed

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WO2008050233A1 (fr)	2008-05-02	Combinaison herbicide
DK2091332T3 (en)	2016-08-29	HERBICID COMBINATIONS CONTAINING AMIDOSULFURON AND A PYRIDINE HERBICID
JP2008542313A (ja)	2008-11-27	油性懸濁製剤
EP0798960B1 (fr)	2006-04-26	Compositions herbicides comprenant un dérivé de sulfonylurée et d'urée
NL7906019A (nl)	1980-04-15	Carbaminezuurfenylesters, werkwijze voor het bereiden daarvan alsmede herbiciden, die deze verbindingen bevatten.
KR20220155358A (ko)	2022-11-22	메틸 (2r＊,4r＊)-4-[[(5s)-3-(3,5-디플루오로페닐)-5-비닐-4h-이속사졸-5-카르보닐]아미노]테트라히드로푸란-2-카르복실레이트의 결정 형태 및 이들의 제초적 상승 효과
US4344790A (en)	1982-08-17	Carbaminic acid esters with herbicidal properties
EP0000051A1 (fr)	1978-12-20	N-acylméthyl-chloroacétanilides, procédé pour leur préparation et leur utilisation comme herbicides.
CH640518A5 (de)	1984-01-13	1,2,3-triazolcarbonsaeureamide sowie diese enthaltende biozide mittel.
EP0013429B1 (fr)	1983-07-20	Herbicides préémergents et postémergents dont la structure active est une N-(triméthyle-cyclohexène-1-yl)-N-isopropyle-alpha-chloracétamide
CA1120942A (fr)	1982-03-30	.sup.m-anilide-urethanes
US10149474B2 (en)	2018-12-11	Herbicidal compositions comprising isoxaflutole and diflufenican
DE3724467A1 (de)	1989-02-02	6-chlorbenzoxazolyl-oxyacetanilide
NO126458B (fr)	1973-02-12
WO1994018177A1 (fr)	1994-08-18	Urees arylaminosulfonyliques
DE3315601A1 (de)	1984-10-31	N-cyclohexadienyl-chloracetamide
DE2828331A1 (de)	1980-01-10	Mittel zur selektiven unkrautbekaempfung
CH583509A5 (fr)	1977-01-14
JP2014097947A (ja)	2014-05-29	スルホキシイミノピラゾール誘導体およびこれを有効成分とする殺虫剤
EP0529292A2 (fr)	1993-03-03	Aralkylsulfonyl-aminoguanidinoazines substitués comme herbizides
EP2486797A1 (fr)	2012-08-15	Utilisation de matières actives de traitement de semences issues du groupe des insecticides à base de carbamates en tant que phytoprotecteur pour des herbicides oxadiazolones
DE3334421A1 (de)	1985-04-18	Herbizide mittel enthaltend metribuzin in kombination mit cyclohexancarbonsaeure-morpholid
BG61491B2 (bg)	1997-09-30	Флуороалкоксиамино триазини за контрол върху плевелите при захарното цвекло
UA111319C2 (uk)	2016-04-25	Застосування агрохімічних сумішей для збільшення життєздатності рослини