DD141991A5 - Pflanzenschutzmittel - Google Patents

Pflanzenschutzmittel Download PDF

Info

Publication number: DD141991A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; trifluoromethyl; trifluoromethylphenyl; weight; development
Prior art date: 1978-02-14

Application number

DD79210946A

Other languages

German (de)

English (en)

Inventor

Wilhelm Sirrenberg

Erich Klauke

Wilhelm Brandes

Peter Roessler

Original Assignee

Bayer 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.)

1978-02-14

Filing date

1979-02-09

Publication date

1980-06-04

1979-02-09 Application filed by Bayer Ag filed Critical Bayer Ag

1980-06-04 Publication of DD141991A5 publication Critical patent/DD141991A5/de

Links

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239000004113 Sepiolite Substances 0.000 description 1
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244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
241000256247 Spodoptera exigua Species 0.000 description 1
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241000511627 Tipula paludosa Species 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
241001238451 Tortrix viridana Species 0.000 description 1
241000018137 Trialeurodes vaporariorum Species 0.000 description 1
241001414833 Triatoma Species 0.000 description 1
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241000255993 Trichoplusia ni Species 0.000 description 1
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241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
241000228452 Venturia inaequalis Species 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
241001274788 Viteus vitifoliae Species 0.000 description 1
235000013447 Xanthosoma atrovirens Nutrition 0.000 description 1
240000001781 Xanthosoma sagittifolium Species 0.000 description 1
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235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
241001414985 Zygentoma Species 0.000 description 1
CGCOVQSKNBEYNN-UHFFFAOYSA-N [4-(trifluoromethyl)phenyl]urea Chemical compound NC(=O)NC1=CC=C(C(F)(F)F)C=C1 CGCOVQSKNBEYNN-UHFFFAOYSA-N 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
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230000009471 action Effects 0.000 description 1
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239000000443 aerosol Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
238000010171 animal model Methods 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
239000001273 butane Substances 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
229910002091 carbon monoxide Inorganic materials 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
229910052801 chlorine Chemical group 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
150000001913 cyanates Chemical class 0.000 description 1
230000002950 deficient Effects 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
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
229910000397 disodium phosphate Inorganic materials 0.000 description 1
235000019800 disodium phosphate Nutrition 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000008393 encapsulating agent Substances 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
230000012173 estrus Effects 0.000 description 1
DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
230000003631 expected effect Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
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238000001914 filtration Methods 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000000446 fuel Substances 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
231100000162 fungitoxic Toxicity 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003502 gasoline Substances 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
239000003595 mist Substances 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
230000000877 morphologic effect Effects 0.000 description 1
230000004660 morphological change Effects 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
150000002825 nitriles Chemical class 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000011368 organic material Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
230000003071 parasitic effect Effects 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
235000019319 peptone Nutrition 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000002243 precursor Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
108090000623 proteins and genes Proteins 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
239000010453 quartz Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
230000009467 reduction Effects 0.000 description 1
239000011435 rock Substances 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000779 smoke Substances 0.000 description 1
239000001488 sodium phosphate Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
239000011782 vitamin Substances 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
150000003722 vitamin derivatives Chemical class 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/48—Y being a hydrogen or a carbon atom
- C07C275/50—Y being a hydrogen or an acyclic carbon atom

Landscapes

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

DD79210946A 1978-02-14 1979-02-09 Pflanzenschutzmittel DD141991A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782806213 DE2806213A1 (de)	1978-02-14	1978-02-14	N-(omega-chloralkanoyl)-n'-trifluormethylphenyl-harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschutzmittel

Publications (1)

Publication Number	Publication Date
DD141991A5 true DD141991A5 (de)	1980-06-04

Family

ID=6031934

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79210946A DD141991A5 (de)	1978-02-14	1979-02-09	Pflanzenschutzmittel

Country Status (14)

Country	Link
US (1)	US4225618A (fr)
EP (1)	EP0003766A1 (fr)
JP (1)	JPS54117438A (fr)
AU (1)	AU4420279A (fr)
BR (1)	BR7900872A (fr)
CA (1)	CA1099741A (fr)
DD (1)	DD141991A5 (fr)
DE (1)	DE2806213A1 (fr)
DK (1)	DK59679A (fr)
ES (1)	ES477659A1 (fr)
IL (1)	IL56647A0 (fr)
PL (1)	PL213398A1 (fr)
PT (1)	PT69214A (fr)
ZA (1)	ZA79625B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2004106292A1 (fr) *	2003-05-28	2004-12-09	Imotep Inc.	Composes d'uree haloethyle et leur utilisation en vue d'attenuer, d'inhiber ou de prevenir la proliferation cellulaire pathogene non cancereuse et les maladies y etant associees
CA2568607A1 (fr) *	2003-05-28	2004-12-09	Imotep Inc.	Composes d'uree haloethyle et leur utilisation en vue d'attenuer, d'inhiber ou de prevenir la migration de cellules cancereuses

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2801200A (en) *	1952-01-08	1957-07-30	Shell Dev	Method of protecting plants from fungi by employing nu-haloacyl urea
DE1161078B (de) *	1960-05-28	1964-01-09	Hoechst Ag	Mittel zur Bekaempfung von Insekten, Spinnen und Milben, deren Eiern und von Pilzen
US3318947A (en) *	1962-09-04	1967-05-09	Monsanto Co	N-(alpha, alpha, alpha-trichloroacetyl)carbamates
DE2512171A1 (de) *	1975-03-20	1976-10-14	Bayer Ag	2,3-dihalogen-alkanoyl-harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als fungizide

1978
- 1978-02-14 DE DE19782806213 patent/DE2806213A1/de not_active Withdrawn
1979
- 1979-02-06 EP EP79100340A patent/EP0003766A1/fr not_active Withdrawn
- 1979-02-08 US US06/010,289 patent/US4225618A/en not_active Expired - Lifetime
- 1979-02-09 DD DD79210946A patent/DD141991A5/de unknown
- 1979-02-12 PT PT7969214A patent/PT69214A/pt unknown
- 1979-02-12 IL IL56647A patent/IL56647A0/xx unknown
- 1979-02-13 DK DK59679A patent/DK59679A/da unknown
- 1979-02-13 AU AU44202/79A patent/AU4420279A/en not_active Abandoned
- 1979-02-13 PL PL21339879A patent/PL213398A1/xx unknown
- 1979-02-13 JP JP1440979A patent/JPS54117438A/ja active Pending
- 1979-02-13 ES ES477659A patent/ES477659A1/es not_active Expired
- 1979-02-13 ZA ZA79625A patent/ZA79625B/xx unknown
- 1979-02-13 CA CA321,371A patent/CA1099741A/fr not_active Expired
- 1979-02-13 BR BR7900872A patent/BR7900872A/pt unknown

Also Published As

Publication number	Publication date
DE2806213A1 (de)	1979-08-16
CA1099741A (fr)	1981-04-21
PL213398A1 (fr)	1980-06-16
DK59679A (da)	1979-08-15
US4225618A (en)	1980-09-30
EP0003766A1 (fr)	1979-09-05
BR7900872A (pt)	1979-09-11
ZA79625B (en)	1980-03-26
PT69214A (en)	1979-03-01
AU4420279A (en)	1979-08-23
IL56647A0 (en)	1979-05-31
ES477659A1 (es)	1979-08-01
JPS54117438A (en)	1979-09-12

Publication	Publication Date	Title
EP0093976B1 (fr)	1986-09-10	Urées et thiourées 2,4-dihalogenbenzoyles, procédés pour leur fabrication et leur utilisation comme pesticides
EP0003099B1 (fr)	1981-09-16	N-phényl, N'(2-chloro-6-fluoro benzoyle)-urées, leurs procédés de préparation et leur utilisation comme insecticides
DE2601780B2 (de)	1979-07-26	N-Phenyl-N'-benzoylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0008435B1 (fr)	1982-05-12	N-Phényl-N'-benzoyle-thiourées substituées, procédé pour leur préparation et leur utilisation comme pesticides
DE2637947C2 (de)	1985-09-19	Tetrafluor-1,3-benzodioxanyl-benzoylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0042533B1 (fr)	1984-03-14	Benzoyl(thio)urées substituées, leurs procédés de préparation et leur application comme pesticides
EP0007541B1 (fr)	1981-09-09	Acides 5-phénylcarbamoyl-barbituriques substitués, procédé pour leur préparation et leur utilisation comme insecticides
EP0009762A1 (fr)	1980-04-16	N-Benzoyle N'-tert. alcoxycarbonylphényle(thio)urées substituées, procédés pour leur préparation et leur utilisation comme insecticides
CH634303A5 (de)	1983-01-31	Phenylcarbamoyl-2-pyrazoline, verfahren zu deren herstellung sowie diese verbindungen enthaltende insektizide.
CH634304A5 (de)	1983-01-31	Phenylcarbamoyl-pyrazoline, verfahren zu deren herstellung sowie die verbindungen enthaltende insektizide.
EP0316845B1 (fr)	1994-01-19	Dérivés de 1,2,3,4-tétrahydro-5-nitropyrimidine
CH627445A5 (de)	1982-01-15	Verfahren zur herstellung neuer substituierter benzoylureidodiphenylaether und ihre verwendung zur bekaempfung von insekten sowie insektizide mittel.
EP0123861B1 (fr)	1988-04-20	Dérivés d'urée
EP0122449B1 (fr)	1987-06-03	Urées benzoyles
EP0008762B1 (fr)	1981-10-21	Esters pyrimidinyliques d'acide N,N-diméthylcarbamique, procédé pour leur préparation et leur utilisation comme pesticides
EP0017066B1 (fr)	1982-04-28	Esters de l'acide N,N-diméthyl-O-pyrazolyl carbamique, leur procédé de préparation et leur application comme pesticides
EP0189043B1 (fr)	1989-03-08	Furazans substitués
EP0318782B1 (fr)	1993-01-20	Benzoyl(thio)urées substituées
DE3622862A1 (de)	1988-01-21	Substituierte furazane
EP0009103B1 (fr)	1981-04-29	N-(O-éthyl-S-n-propyl-(di)thiophosphoryloxy)-naphtalimides, procédé pour leur préparation, compositions pesticides les contenant, leur préparation et leur utilisation
EP0197280B1 (fr)	1989-06-07	Benzoylurées
US4225618A (en)	1980-09-30	Combating plant pests with N-(ω-chloro-alkanoyl)-N'-trifluoromethylphenyl-ureas
EP0316734B1 (fr)	1991-07-03	Furazannyl urées
DE2739192A1 (de)	1979-03-08	Indan-4-yl-n-alkyl-carbaminsaeureester, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenschutzmittel
DE3438919A1 (de)	1986-04-24	Substituierte phenyl-carbaminsaeureester