DD202494A5 - Schaedlingsbekaempfungsmittel - Google Patents

Schaedlingsbekaempfungsmittel Download PDF

Info

Publication number: DD202494A5
Authority: DD; German Democratic Republic
Prior art keywords: alkyl; formula; spp; exp5; optionally substituted
Prior art date: 1981-04-24

Application number

DD82239193A

Other languages

German (de)

English (en)

Inventor

Hans-Ludwig Elbe

Ingeborg Hammann

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.)

1981-04-24

Filing date

1982-04-21

Publication date

1983-09-21

1982-04-21 Application filed by Bayer Ag filed Critical Bayer Ag

1983-09-21 Publication of DD202494A5 publication Critical patent/DD202494A5/de

Links

125000000217 alkyl group Chemical group 0.000 claims abstract description 34
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 16
239000001257 hydrogen Substances 0.000 claims abstract description 12
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
229910052736 halogen Inorganic materials 0.000 claims abstract description 11
150000002367 halogens Chemical group 0.000 claims abstract description 9
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 7
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 6
239000000575 pesticide Substances 0.000 claims abstract description 6
125000003342 alkenyl group Chemical group 0.000 claims abstract description 5
125000000304 alkynyl group Chemical group 0.000 claims abstract description 5
239000003795 chemical substances by application Substances 0.000 claims abstract description 5
125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 4
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims abstract description 4
150000002431 hydrogen Chemical class 0.000 claims abstract 4
238000000034 method Methods 0.000 claims description 37
238000002360 preparation method Methods 0.000 claims description 17
YTFJICHTJRMNJX-UHFFFAOYSA-N NC(=O)C1CCSC1=NO Chemical class NC(=O)C1CCSC1=NO YTFJICHTJRMNJX-UHFFFAOYSA-N 0.000 claims description 9
241000607479 Yersinia pestis Species 0.000 claims description 8
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 5
239000004606 Fillers/Extenders Substances 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 2
239000004480 active ingredient Substances 0.000 abstract description 5
239000000463 material Substances 0.000 abstract description 4
230000000895 acaricidal effect Effects 0.000 abstract description 3
230000000749 insecticidal effect Effects 0.000 abstract description 3
101100354192 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) exp5 gene Proteins 0.000 abstract 6
101150109310 msrAB1 gene Proteins 0.000 abstract 3
101100439974 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) clpE gene Proteins 0.000 abstract 2
101100242909 Streptococcus pneumoniae (strain ATCC BAA-255 / R6) pbpA gene Proteins 0.000 abstract 1
101100269618 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) aliA gene Proteins 0.000 abstract 1
101100505001 Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) glpO gene Proteins 0.000 abstract 1
101100072620 Streptomyces griseus ind2 gene Proteins 0.000 abstract 1
150000001875 compounds Chemical class 0.000 description 38
239000000460 chlorine Substances 0.000 description 26
-1 Alkoxyalky1 Chemical group 0.000 description 16
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
238000006243 chemical reaction Methods 0.000 description 14
239000002904 solvent Substances 0.000 description 14
125000004432 carbon atom Chemical group C* 0.000 description 13
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
229910052801 chlorine Inorganic materials 0.000 description 10
239000000203 mixture Substances 0.000 description 10
239000007858 starting material Substances 0.000 description 10
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 9
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
239000003995 emulsifying agent Substances 0.000 description 8
125000004435 hydrogen atom Chemical class [H]* 0.000 description 8
150000002576 ketones Chemical class 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 7
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 7
229910052794 bromium Inorganic materials 0.000 description 7
239000007800 oxidant agent Substances 0.000 description 7
150000003254 radicals Chemical class 0.000 description 7
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 6
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
239000011230 binding agent Substances 0.000 description 6
229910052731 fluorine Inorganic materials 0.000 description 6
239000011737 fluorine Substances 0.000 description 6
238000009472 formulation Methods 0.000 description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
150000002923 oximes Chemical class 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
239000003960 organic solvent Substances 0.000 description 5
240000007124 Brassica oleracea Species 0.000 description 4
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
125000001309 chloro group Chemical group Cl* 0.000 description 4
239000003085 diluting agent Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
238000002955 isolation Methods 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
241000254173 Coleoptera Species 0.000 description 3
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 3
239000002585 base Substances 0.000 description 3
239000000969 carrier Substances 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
229910000037 hydrogen sulfide Inorganic materials 0.000 description 3
239000012948 isocyanate Substances 0.000 description 3
150000002513 isocyanates Chemical class 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
230000003647 oxidation Effects 0.000 description 3
238000007254 oxidation reaction Methods 0.000 description 3
230000000361 pesticidal effect Effects 0.000 description 3
239000000047 product Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
241001124076 Aphididae Species 0.000 description 2
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
235000011303 Brassica alboglabra Nutrition 0.000 description 2
235000011302 Brassica oleracea Nutrition 0.000 description 2
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
241000251730 Chondrichthyes Species 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
241000258937 Hemiptera Species 0.000 description 2
WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
241000257303 Hymenoptera Species 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
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ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
241000256248 Spodoptera Species 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
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241001454294 Tetranychus Species 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
150000001649 bromium compounds Chemical class 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000000539 dimer Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000975 dye Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000004049 embossing Methods 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
239000006260 foam Substances 0.000 description 2
239000007789 gas Substances 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
150000008282 halocarbons Chemical class 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
LULAYUGMBFYYEX-UHFFFAOYSA-N metachloroperbenzoic acid Natural products OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 2
HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 2
239000011707 mineral Substances 0.000 description 2
235000010755 mineral Nutrition 0.000 description 2
VDJNKPIYLQIANW-UHFFFAOYSA-N n-[4-(chloromethyl)-4-methylthiolan-3-ylidene]hydroxylamine Chemical compound ClCC1(C)CSCC1=NO VDJNKPIYLQIANW-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
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125000001424 substituent group Chemical group 0.000 description 2
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/32—Oxygen 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/36—Nitrogen atoms

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Environmental Sciences (AREA)
Zoology (AREA)
Wood Science & Technology (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Veterinary Medicine (AREA)
Agronomy & Crop Science (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Animal Behavior & Ethology (AREA)
Chemical Kinetics & Catalysis (AREA)
Pharmacology & Pharmacy (AREA)
Tropical Medicine & Parasitology (AREA)
General Chemical & Material Sciences (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Heterocyclic Compounds Containing Sulfur Atoms (AREA)

DD82239193A 1981-04-24 1982-04-21 Schaedlingsbekaempfungsmittel DD202494A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813116297 DE3116297A1 (de)	1981-04-24	1981-04-24	Substituierte

Publications (1)

Publication Number	Publication Date
DD202494A5 true DD202494A5 (de)	1983-09-21

Family

ID=6130737

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82239193A DD202494A5 (de)	1981-04-24	1982-04-21	Schaedlingsbekaempfungsmittel

Country Status (13)

Country	Link
US (1)	US4501753A (fr)
EP (1)	EP0063742A3 (fr)
JP (1)	JPS57181080A (fr)
AU (1)	AU8296582A (fr)
BR (1)	BR8202333A (fr)
DD (1)	DD202494A5 (fr)
DE (1)	DE3116297A1 (fr)
DK (1)	DK183682A (fr)
ES (1)	ES511655A0 (fr)
IL (1)	IL65561A0 (fr)
PL (1)	PL236126A1 (fr)
PT (1)	PT74746B (fr)
ZA (1)	ZA822776B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE236091C (fr) *	1985-07-29

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3317562A (en) *	1965-02-23	1967-05-02	American Cyanamid Co	2-oximinothiolanes and related compounds
CA946848A (en) *	1969-07-07	1974-05-07	Thomas A. Magee	Pesticidal compositions of 3-(n-alky-carbamyloximino) - saturated heterocyclic compounds
US3755364A (en) *	1972-02-02	1973-08-28	Diamond Shamrock Corp	3-(n-carbamyloximino)-saturated thioheterocyclic compounds
US4232035A (en) *	1975-12-30	1980-11-04	Union Carbide Corporation	Carbamate pesticidal compounds compositions and methods of use

1981
- 1981-04-24 DE DE19813116297 patent/DE3116297A1/de not_active Withdrawn
1982
- 1982-04-05 US US06/365,929 patent/US4501753A/en not_active Expired - Fee Related
- 1982-04-13 EP EP82103116A patent/EP0063742A3/fr not_active Withdrawn
- 1982-04-14 PT PT74746A patent/PT74746B/pt unknown
- 1982-04-20 JP JP57064860A patent/JPS57181080A/ja active Pending
- 1982-04-21 DD DD82239193A patent/DD202494A5/de unknown
- 1982-04-21 IL IL65561A patent/IL65561A0/xx unknown
- 1982-04-23 ES ES511655A patent/ES511655A0/es active Granted
- 1982-04-23 PL PL23612682A patent/PL236126A1/xx unknown
- 1982-04-23 BR BR8202333A patent/BR8202333A/pt unknown
- 1982-04-23 AU AU82965/82A patent/AU8296582A/en not_active Abandoned
- 1982-04-23 DK DK183682A patent/DK183682A/da not_active Application Discontinuation
- 1982-04-23 ZA ZA822776A patent/ZA822776B/xx unknown

Also Published As

Publication number	Publication date
ES8304113A1 (es)	1983-02-16
IL65561A0 (en)	1982-07-30
EP0063742A2 (fr)	1982-11-03
DE3116297A1 (de)	1982-11-11
JPS57181080A (en)	1982-11-08
EP0063742A3 (fr)	1982-12-29
BR8202333A (pt)	1983-04-05
PT74746A (en)	1982-05-01
PL236126A1 (en)	1983-06-20
ES511655A0 (es)	1983-02-16
US4501753A (en)	1985-02-26
ZA822776B (en)	1983-03-30
AU8296582A (en)	1982-10-28
DK183682A (da)	1982-10-25
PT74746B (en)	1983-11-08

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DE3616681A1 (de)	1987-11-19	1-aralkylpyrazole
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EP0000198A1 (fr)	1979-01-10	Esters d'acide N,N-dialcoyl-0-pyrimidinyl- carbamique procédé pour leur préparation et leur utilisation comme insecticides
EP0050283B1 (fr)	1984-02-22	Esters de l'acide hydroxamique, procédé pour leur préparation, leur application comme pesticides et produits intermédiaires intervenant dans ce procédé
DD202494A5 (de)	1983-09-21	Schaedlingsbekaempfungsmittel
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EP0024329A2 (fr)	1981-03-04	2-Carbamoyloximino-butanes substitués, procédé pour leur préparation et leur utilisation comme pesticides
DE3445465A1 (de)	1986-06-19	Pyrimidinyl-thionophosphorsaeureester
EP0087561B1 (fr)	1986-01-29	Esters de l'acide N,N-dimethyl-0-(1-carbamoyl-5-pyrazolyl)-carbamique, leur procédé de préparation et leur application comme biocides
DE3224787A1 (de)	1984-01-05	Oximcarbamate, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
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EP0007987A1 (fr)	1980-02-20	Carbamoyloximino-1-méthylthio-butanes N-sulfénylés, procédé pour leur préparation et leur utilisation comme insecticides
EP0092721A1 (fr)	1983-11-02	Carbamates N-sulfényles, procédé pour leur préparation et leur utilisation comme pesticides
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