DD201968A5 - Carbamatderivate enthaltende insektizide, antimilben- oder nematozide zusammensetzungen - Google Patents

Carbamatderivate enthaltende insektizide, antimilben- oder nematozide zusammensetzungen Download PDF

Info

Publication number: DD201968A5
Authority: DD; German Democratic Republic
Prior art keywords: ppm; group; carbon atoms; cooc; mol
Prior art date: 1981-06-02

Application number

DD81235784A

Other languages

German (de)

English (en)

Inventor

Takeshi Goto

Akira Tanaka

Nobuyoshi Asai

Hisashi Takao

Takashi Soeda

Sadahiko Iida

Norio Yasudomi

Norio Osaki

Tadateru Murata

Mitsuyasu Kawada

Hiroyuki Yatako

Original Assignee

Otsuka 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.)

1981-06-02

Filing date

1981-12-15

Publication date

1983-08-24

1981-06-02 Priority claimed from JP8509481A external-priority patent/JPS6049638B2/ja

1981-06-02 Priority claimed from JP8509381A external-priority patent/JPS6049637B2/ja

1981-12-15 Application filed by Otsuka Chemical Co Ltd filed Critical Otsuka Chemical Co Ltd

1983-08-24 Publication of DD201968A5 publication Critical patent/DD201968A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 47
150000004657 carbamic acid derivatives Chemical class 0.000 title claims abstract description 11
230000001069 nematicidal effect Effects 0.000 title claims abstract description 4
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239000005645 nematicide Substances 0.000 title 1
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125000004432 carbon atom Chemical group C* 0.000 claims description 37
125000000217 alkyl group Chemical group 0.000 claims description 19
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125000002947 alkylene group Chemical group 0.000 claims description 6
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125000000753 cycloalkyl group Chemical group 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
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239000001273 butane Substances 0.000 description 1
HVNPFQOMBNYVMB-UHFFFAOYSA-N butyl 2-(methylamino)acetate Chemical compound CCCCOC(=O)CNC HVNPFQOMBNYVMB-UHFFFAOYSA-N 0.000 description 1
GBZDFUBJNQPZOC-UHFFFAOYSA-N butyl 2-(propan-2-ylamino)propanoate Chemical compound CCCCOC(=O)C(C)NC(C)C GBZDFUBJNQPZOC-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000005520 cutting process Methods 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
GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000000975 dye Substances 0.000 description 1
SBPUJTNHAUBDKF-UHFFFAOYSA-N ethyl 2-(2-cyanoethylamino)acetate Chemical compound CCOC(=O)CNCCC#N SBPUJTNHAUBDKF-UHFFFAOYSA-N 0.000 description 1
QJERSMYDZNFZDK-UHFFFAOYSA-N ethyl 2-(2-cyanoethylamino)propanoate Chemical compound CCOC(=O)C(C)NCCC#N QJERSMYDZNFZDK-UHFFFAOYSA-N 0.000 description 1
XJBLZCHTARFLLD-UHFFFAOYSA-N ethyl 2-(2-methylpropylamino)acetate Chemical compound CCOC(=O)CNCC(C)C XJBLZCHTARFLLD-UHFFFAOYSA-N 0.000 description 1
JZCIUMVCWIEEQX-UHFFFAOYSA-N ethyl 2-(3-methylanilino)acetate Chemical compound CCOC(=O)CNC1=CC=CC(C)=C1 JZCIUMVCWIEEQX-UHFFFAOYSA-N 0.000 description 1
XDAVIDCHNYCQCT-UHFFFAOYSA-N ethyl 2-(3-methylbutylamino)propanoate Chemical compound CCOC(=O)C(C)NCCC(C)C XDAVIDCHNYCQCT-UHFFFAOYSA-N 0.000 description 1
TZJRPKDPYLAMJZ-UHFFFAOYSA-N ethyl 2-(4-methoxyanilino)acetate Chemical compound CCOC(=O)CNC1=CC=C(OC)C=C1 TZJRPKDPYLAMJZ-UHFFFAOYSA-N 0.000 description 1
KTRUZIMBKAONKB-UHFFFAOYSA-N ethyl 2-(butan-2-ylamino)acetate Chemical compound CCOC(=O)CNC(C)CC KTRUZIMBKAONKB-UHFFFAOYSA-N 0.000 description 1
HRFATYXNXXEKNO-UHFFFAOYSA-N ethyl 2-(butan-2-ylamino)propanoate Chemical compound CCOC(=O)C(C)NC(C)CC HRFATYXNXXEKNO-UHFFFAOYSA-N 0.000 description 1
OJFGRDHUZSJJPB-UHFFFAOYSA-N ethyl 2-(butylamino)acetate Chemical compound CCCCNCC(=O)OCC OJFGRDHUZSJJPB-UHFFFAOYSA-N 0.000 description 1
HJHAOMCORINKOB-UHFFFAOYSA-N ethyl 2-(cyanomethylamino)acetate Chemical compound CCOC(=O)CNCC#N HJHAOMCORINKOB-UHFFFAOYSA-N 0.000 description 1
DITDYMTYUDGGGF-UHFFFAOYSA-N ethyl 2-(cyanomethylamino)propanoate Chemical compound CCOC(=O)C(C)NCC#N DITDYMTYUDGGGF-UHFFFAOYSA-N 0.000 description 1
NHRFJPKXIYYFMX-UHFFFAOYSA-N ethyl 2-(cyclohexylamino)acetate Chemical compound CCOC(=O)CNC1CCCCC1 NHRFJPKXIYYFMX-UHFFFAOYSA-N 0.000 description 1
UPPDUARXWJEKFZ-UHFFFAOYSA-N ethyl 2-(cyclohexylamino)propanoate Chemical compound CCOC(=O)C(C)NC1CCCCC1 UPPDUARXWJEKFZ-UHFFFAOYSA-N 0.000 description 1
ORKAHUKYJCNDDI-UHFFFAOYSA-N ethyl 2-(ethoxycarbonylamino)acetate Chemical compound CCOC(=O)CNC(=O)OCC ORKAHUKYJCNDDI-UHFFFAOYSA-N 0.000 description 1
OMECLFTURFUIIJ-UHFFFAOYSA-N ethyl 2-(ethoxycarbonylamino)propanoate Chemical compound CCOC(=O)NC(C)C(=O)OCC OMECLFTURFUIIJ-UHFFFAOYSA-N 0.000 description 1
NRMPJIHWGVBZBB-UHFFFAOYSA-N ethyl 2-(ethylamino)acetate Chemical compound CCNCC(=O)OCC NRMPJIHWGVBZBB-UHFFFAOYSA-N 0.000 description 1
LCMDFUNTIZKNJK-UHFFFAOYSA-N ethyl 2-(hexylamino)propanoate Chemical compound CCCCCCNC(C)C(=O)OCC LCMDFUNTIZKNJK-UHFFFAOYSA-N 0.000 description 1
LNYUJLIYAHJNNO-UHFFFAOYSA-N ethyl 2-(methoxycarbonylamino)acetate Chemical compound CCOC(=O)CNC(=O)OC LNYUJLIYAHJNNO-UHFFFAOYSA-N 0.000 description 1
BTKSUULMJNNXHG-UHFFFAOYSA-N ethyl 2-(methylamino)acetate Chemical compound CCOC(=O)CNC BTKSUULMJNNXHG-UHFFFAOYSA-N 0.000 description 1
KHRLPZJTPHCMSQ-UHFFFAOYSA-N ethyl 2-(methylamino)propanoate Chemical compound CCOC(=O)C(C)NC KHRLPZJTPHCMSQ-UHFFFAOYSA-N 0.000 description 1
CWPWNWCAOJRJJT-UHFFFAOYSA-N ethyl 2-(phenoxycarbonylamino)acetate Chemical compound CCOC(=O)CNC(=O)OC1=CC=CC=C1 CWPWNWCAOJRJJT-UHFFFAOYSA-N 0.000 description 1
ROGQHXXFNVNMSC-UHFFFAOYSA-N ethyl 2-(propan-2-ylamino)acetate Chemical compound CCOC(=O)CNC(C)C ROGQHXXFNVNMSC-UHFFFAOYSA-N 0.000 description 1
JBIONIMUHCHUOW-UHFFFAOYSA-N ethyl 2-(propan-2-ylamino)propanoate Chemical compound CCOC(=O)C(C)NC(C)C JBIONIMUHCHUOW-UHFFFAOYSA-N 0.000 description 1
XKFRTCBBCLBPOA-UHFFFAOYSA-N ethyl 2-(propanoylamino)acetate Chemical compound CCOC(=O)CNC(=O)CC XKFRTCBBCLBPOA-UHFFFAOYSA-N 0.000 description 1
IIBDNCRATXAUMF-UHFFFAOYSA-N ethyl 2-[(2-ethoxy-2-oxoethyl)amino]propanoate Chemical compound CCOC(=O)CNC(C)C(=O)OCC IIBDNCRATXAUMF-UHFFFAOYSA-N 0.000 description 1
XYVZUPHHGNHQHN-UHFFFAOYSA-N ethyl 2-[(4-chlorobenzoyl)amino]acetate Chemical compound CCOC(=O)CNC(=O)C1=CC=C(Cl)C=C1 XYVZUPHHGNHQHN-UHFFFAOYSA-N 0.000 description 1
WZLAJHNLDCWPGH-UHFFFAOYSA-N ethyl 2-[(4-methylphenyl)sulfonylamino]acetate Chemical compound CCOC(=O)CNS(=O)(=O)C1=CC=C(C)C=C1 WZLAJHNLDCWPGH-UHFFFAOYSA-N 0.000 description 1
AMBDTBHJFINMSE-UHFFFAOYSA-N ethyl 2-acetamidoacetate Chemical compound CCOC(=O)CNC(C)=O AMBDTBHJFINMSE-UHFFFAOYSA-N 0.000 description 1
PTXRQIPIELXJFH-UHFFFAOYSA-N ethyl 2-benzamidoacetate Chemical compound CCOC(=O)CNC(=O)C1=CC=CC=C1 PTXRQIPIELXJFH-UHFFFAOYSA-N 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
LXRRVDLNCROODH-UHFFFAOYSA-N ethyl n-(2-cyanoethyl)carbamate Chemical compound CCOC(=O)NCCC#N LXRRVDLNCROODH-UHFFFAOYSA-N 0.000 description 1
AHGQESFVDCNOGJ-UHFFFAOYSA-N ethyl n-(cyanomethyl)carbamate Chemical compound CCOC(=O)NCC#N AHGQESFVDCNOGJ-UHFFFAOYSA-N 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
239000002316 fumigant Substances 0.000 description 1
231100000086 high toxicity Toxicity 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
238000005470 impregnation 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
239000004571 lime Substances 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
NELVBJNELOBGSL-UHFFFAOYSA-N methyl 2-(butylamino)propanoate Chemical compound CCCCNC(C)C(=O)OC NELVBJNELOBGSL-UHFFFAOYSA-N 0.000 description 1
LSZJHXHDMLYQFO-UHFFFAOYSA-N methyl 2-(propan-2-ylamino)propanoate Chemical compound COC(=O)C(C)NC(C)C LSZJHXHDMLYQFO-UHFFFAOYSA-N 0.000 description 1
DRMGMMWXWKLKAI-UHFFFAOYSA-N methyl n-(cyanomethyl)carbamate Chemical compound COC(=O)NCC#N DRMGMMWXWKLKAI-UHFFFAOYSA-N 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000012544 monitoring process Methods 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
239000012452 mother liquor Substances 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
230000024121 nodulation Effects 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
239000001294 propane Substances 0.000 description 1
WOMAZEJKVZLLFE-UHFFFAOYSA-N propionylglycine Chemical compound CCC(=O)NCC(O)=O WOMAZEJKVZLLFE-UHFFFAOYSA-N 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
238000000926 separation method Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
238000000638 solvent extraction Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/86—Benzo [b] furans; Hydrogenated benzo [b] furans with an oxygen atom directly attached in position 7
- 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
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof

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

DD81235784A 1981-06-02 1981-12-15 Carbamatderivate enthaltende insektizide, antimilben- oder nematozide zusammensetzungen DD201968A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP8509481A JPS6049638B2 (ja)	1981-06-02	1981-06-02	カ−バメイト系殺虫剤
JP8509381A JPS6049637B2 (ja)	1981-06-02	1981-06-02	カ−バメイト系殺虫剤

Publications (1)

Publication Number	Publication Date
DD201968A5 true DD201968A5 (de)	1983-08-24

Family

ID=26426116

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD81235784A DD201968A5 (de)	1981-06-02	1981-12-15	Carbamatderivate enthaltende insektizide, antimilben- oder nematozide zusammensetzungen
DD81244667A DD206779A5 (de)	1981-06-02	1981-12-15	Verfahren zur herstellung von carbamatderivaten

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
DD81244667A DD206779A5 (de)	1981-06-02	1981-12-15	Verfahren zur herstellung von carbamatderivaten

Country Status (3)

Country	Link
DD (2)	DD201968A5 (tr)
OA (1)	OA06912A (tr)
TR (1)	TR20962A (tr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1986003202A1 (en) *	1984-11-23	1986-06-05	Chinoin Gyógyszer és Vegyészeti Termékek Gyára Rt.	New pesticides

1981
- 1981-09-24 TR TR20962A patent/TR20962A/tr unknown
- 1981-10-01 OA OA57507A patent/OA06912A/xx unknown
- 1981-12-15 DD DD81235784A patent/DD201968A5/de not_active IP Right Cessation
- 1981-12-15 DD DD81244667A patent/DD206779A5/de not_active IP Right Cessation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1986003202A1 (en) *	1984-11-23	1986-06-05	Chinoin Gyógyszer és Vegyészeti Termékek Gyára Rt.	New pesticides

Also Published As

Publication number	Publication date
OA06912A (fr)	1983-05-31
DD206779A5 (de)	1984-02-08
TR20962A (tr)	1983-02-25

Legal Events

Date	Code	Title	Description
2001-05-24	ENJ	Ceased due to non-payment of renewal fee

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DE69028461T2 (de)	1997-02-06	Triazin-derivate und unkrautvertilgungsmittel daraus
DE3853771T2 (de)	1995-10-05	Alkylaminopyrimidin-Derivate, Verfahren zu ihrer Herstellung und diese als aktive Bestandteile enthaltende Insektizide, Akarizide und Fungizide.
DE3713774C2 (de)	1993-10-07	Pyrazol-Derivate, Verfahren zu ihrer Herstellung und diese enthaltende Fungizide
DE3206453C2 (de)	1994-08-18	S-Methyl-N-[(N-methyl-N-(N,N-disubstituierte amino-sulfenyl)-carbamoyl)-oxy]-thioacetimidat-derivate, Verfahren zu deren Herstellung und diese enthaltende insektizide, mitizide oder nematozide Zusammensetzungen
DE3134596C2 (tr)	1990-08-09
DE1667979A1 (de)	1971-07-15	Schaedlingsbekaempfungsmittel,die bestimmte Benzodioxole enthalten,sowie Verfahren zu deren Herstellung
US4413005A (en)	1983-11-01	Carbamate derivatives and insecticidal, miticidal or nematocidal compositions containing the same
DD201968A5 (de)	1983-08-24	Carbamatderivate enthaltende insektizide, antimilben- oder nematozide zusammensetzungen
EP0256407B1 (de)	1991-03-06	Insektizide Mittel
CA1170662A (en)	1984-07-10	Carbamate derivatives, process for preparing same and carbamate insecticides
DE3780574T2 (de)	1993-01-21	3-substituierte 4-fluorophenyl-1-(fluoroalkoxyphenyl-carbamoyl)-pyrazolin-insektizide.
DE69709895T2 (de)	2002-08-01	Hydrazincarboxylat-mitizide und -insectizide
DE3211087C2 (de)	1994-09-08	Aminosulfenylchloridderivate, Verfahren zu deren Herstellung und deren Verwendung
US4788217A (en)	1988-11-29	Pesticidal carbamates
DE2826531C2 (tr)	1988-04-14
DE3033358C2 (de)	1983-12-29	Isovaleriansäure-Derivate, Verfahren zu deren Herstellung und diese enthaltende insektizide und acarizide Mittel
US4109011A (en)	1978-08-22	Insecticide carbamates of n-(polychloroallyl)-amino-phenols
KR850000743B1 (ko)	1985-05-24	카바메이트유도체의 제조방법
CH636361A5 (de)	1983-05-31	Einen isoxazolinonring enthaltende mono- und dithiophosphorsaeureester.
DE2430207A1 (de)	1975-01-16	Schaedlingsbekaempfungsmittel bzw. dessen wirkstoffe
DD145219A5 (de)	1980-12-03	Pflanzenwuchsregulierendes mittel
AT362197B (de)	1981-04-27	Verfahren zur bekaempfung von insekten, milben und nematoden
DE2362333A1 (de)	1974-06-20	Phosphororganische herbizide
AT363726B (de)	1981-08-25	Insektizides und mitizides mittel
DE3305280A1 (de)	1984-08-23	Benzoylhydrazonderivate und sie enthaltende insektizide

DD201968A5 - Carbamatderivate enthaltende insektizide, antimilben- oder nematozide zusammensetzungen - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (2)

Publications (1)

Family

ID=26426116

Family Applications (2)

Family Applications After (1)

Country Status (3)

Cited By (1)

Cited By (1)

Also Published As

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