DD143551A5 - Insektizide mittel - Google Patents

Insektizide mittel Download PDF

Info

Publication number: DD143551A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; alkyl; active; methyl; alkenyl
Prior art date: 1978-04-15

Application number

DD79212191A

Other languages

German (de)

English (en)

Inventor

Volker Mues

Wolfgang Behrenz

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.)

1978-04-15

Filing date

1979-04-12

Publication date

1980-09-03

1979-04-12 Application filed by Bayer Ag filed Critical Bayer Ag

1980-09-03 Publication of DD143551A5 publication Critical patent/DD143551A5/de

Links

239000002917 insecticide Substances 0.000 title claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 14
125000003342 alkenyl group Chemical group 0.000 claims description 11
239000013543 active substance Substances 0.000 claims description 10
125000003118 aryl group Chemical group 0.000 claims description 9
239000004480 active ingredient Substances 0.000 claims description 8
150000003014 phosphoric acid esters Chemical class 0.000 claims description 8
150000001733 carboxylic acid esters Chemical class 0.000 claims description 7
230000000749 insecticidal effect Effects 0.000 claims description 7
150000001350 alkyl halides Chemical class 0.000 claims description 5
239000004606 Fillers/Extenders Substances 0.000 claims description 4
241000238631 Hexapoda Species 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
239000000463 material Substances 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 claims 2
239000003814 drug Substances 0.000 claims 1
229940079593 drug Drugs 0.000 claims 1
-1 for example Chemical class 0.000 description 52
125000004432 carbon atom Chemical group C* 0.000 description 20
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
150000001875 compounds Chemical class 0.000 description 12
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
238000009472 formulation Methods 0.000 description 9
229910052736 halogen Inorganic materials 0.000 description 9
150000002367 halogens Chemical class 0.000 description 9
239000002904 solvent Substances 0.000 description 8
WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 7
150000004657 carbamic acid derivatives Chemical class 0.000 description 7
150000002825 nitriles Chemical class 0.000 description 7
230000002195 synergetic effect Effects 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000001257 hydrogen Substances 0.000 description 6
229910052739 hydrogen Inorganic materials 0.000 description 6
229910052760 oxygen Inorganic materials 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
241001465754 Metazoa Species 0.000 description 5
230000000895 acaricidal effect Effects 0.000 description 5
125000003545 alkoxy group Chemical group 0.000 description 5
150000005528 benzodioxoles Chemical class 0.000 description 5
229910052799 carbon Inorganic materials 0.000 description 5
239000000460 chlorine Substances 0.000 description 5
229910052801 chlorine Inorganic materials 0.000 description 5
239000003085 diluting agent Substances 0.000 description 5
150000003254 radicals Chemical class 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical group C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 description 4
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
239000000969 carrier Substances 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
239000008187 granular material Substances 0.000 description 4
125000001188 haloalkyl group Chemical group 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
239000000843 powder Substances 0.000 description 4
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
LEBXSRJXGRZVLM-UHFFFAOYSA-N 4-methoxy-2-propan-2-ylpyrimidine Chemical compound COC1=CC=NC(C(C)C)=N1 LEBXSRJXGRZVLM-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-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
241000607479 Yersinia pestis Species 0.000 description 3
125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
238000009835 boiling Methods 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
239000000047 product Substances 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
239000007787 solid Substances 0.000 description 3
LMQWOLFVHAMFLR-UHFFFAOYSA-N 3-chloro-4-methylchromen-2-one Chemical compound C1=CC=CC2=C1OC(=O)C(Cl)=C2C LMQWOLFVHAMFLR-UHFFFAOYSA-N 0.000 description 2
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 2
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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
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
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LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
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UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
125000000304 alkynyl group Chemical group 0.000 description 2
JPOXNPPZZKNXOV-UHFFFAOYSA-N bromochloromethane Chemical compound ClCBr JPOXNPPZZKNXOV-UHFFFAOYSA-N 0.000 description 2
244000309464 bull Species 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000012043 crude product Substances 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
125000004663 dialkyl amino group Chemical group 0.000 description 2
125000000532 dioxanyl group Chemical group 0.000 description 2
125000005879 dioxolanyl group Chemical group 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000975 dye Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
239000006260 foam Substances 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate Chemical compound [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 2
239000011707 mineral Substances 0.000 description 2
235000010755 mineral Nutrition 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
229960005235 piperonyl butoxide Drugs 0.000 description 2
XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000007858 starting material Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
125000004953 trihalomethyl group Chemical group 0.000 description 2
238000005292 vacuum distillation Methods 0.000 description 2
239000008096 xylene Substances 0.000 description 2
GDAXJBDYNVDMDF-UHFFFAOYSA-N 1,2,4-benzotriazine Chemical compound N1=NC=NC2=CC=CC=C21 GDAXJBDYNVDMDF-UHFFFAOYSA-N 0.000 description 1
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OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 1
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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
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150000002923 oximes Chemical group 0.000 description 1
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230000000361 pesticidal effect Effects 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
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239000010695 polyglycol Substances 0.000 description 1
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239000011118 polyvinyl acetate Substances 0.000 description 1
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239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
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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
- C07D317/44—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 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—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 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring 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 atoms of the carbocyclic ring
- C07D317/64—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
- A01N43/24—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 two or more hetero atoms
- A01N43/26—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 two or more hetero atoms five-membered rings
- A01N43/28—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 two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
- A01N43/30—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 two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3 with two oxygen atoms in positions 1,3, condensed with a carbocyclic ring
- 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
- C07D317/44—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 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—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 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring 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 atoms of the carbocyclic ring

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

DD79212191A 1978-04-15 1979-04-12 Insektizide mittel DD143551A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782816474 DE2816474A1 (de)	1978-04-15	1978-04-15	Dichlorbenzodioxolderivate, verfahren zu ihrer herstellung und ihre verwendung als synergisten in insektiziden und akariziden mitteln

Publications (1)

Publication Number	Publication Date
DD143551A5 true DD143551A5 (de)	1980-09-03

Family

ID=6037103

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79212191A DD143551A5 (de)	1978-04-15	1979-04-12	Insektizide mittel

Country Status (15)

Country	Link
US (1)	US4250187A (fr)
EP (1)	EP0004895B1 (fr)
JP (1)	JPS54138563A (fr)
AU (1)	AU4607779A (fr)
BR (1)	BR7902212A (fr)
CA (1)	CA1120045A (fr)
DD (1)	DD143551A5 (fr)
DE (2)	DE2816474A1 (fr)
DK (1)	DK153679A (fr)
ES (1)	ES479477A1 (fr)
HU (1)	HU182451B (fr)
IL (1)	IL57058A (fr)
PL (1)	PL214883A1 (fr)
PT (1)	PT69444A (fr)
ZA (1)	ZA791768B (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AT375360B (de) *	1982-12-23	1984-07-25	Gerot Pharmazeutika	Verfahren zur herstellung von neuen 1,3-benzodioxol-derivaten und deren salzen
EP0095454A3 (fr) *	1982-05-13	1985-04-03	Gerot-Pharmazeutika Gesellschaft m.b.H.	Dérivés de pyrogallol substitués sur le noyau
DE4133156A1 (de) *	1991-10-07	1993-04-08	Bayer Ag	Verfahren zur herstellung von fluorsubstituierten aminobenzodioxolen und -benzodioxanen und neue zwischenprodukte
JPH08301704A (ja) *	1995-05-10	1996-11-19	Mitsubishi Corp	工業用防腐防カビ剤組成物及び水中防汚剤組成物
PL1722805T3 (pl) *	2004-01-12	2014-08-29	Akzo Nobel Surface Chemistry Llc	Biologicznie czynne kompozycje z roślin Theacea oraz sposoby ich wytwarzania i zastosowanie

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2878265A (en) *	1956-09-10	1959-03-17	Fmc Corp	Production of methylenedioxyphenyl derivatives
GB1046209A (en) *	1964-07-24	1966-10-19	Shell Int Research	Insecticidal compositions
GB1542641A (en) *	1975-06-30	1979-03-21	Shell Int Research	Wild oat herbicide

1978
- 1978-04-15 DE DE19782816474 patent/DE2816474A1/de not_active Withdrawn
1979
- 1979-03-28 US US06/024,745 patent/US4250187A/en not_active Expired - Lifetime
- 1979-03-31 EP EP79100982A patent/EP0004895B1/fr not_active Expired
- 1979-03-31 DE DE7979100982T patent/DE2960227D1/de not_active Expired
- 1979-04-06 PT PT69444A patent/PT69444A/pt unknown
- 1979-04-10 ES ES479477A patent/ES479477A1/es not_active Expired
- 1979-04-10 BR BR7902212A patent/BR7902212A/pt unknown
- 1979-04-11 IL IL57058A patent/IL57058A/xx unknown
- 1979-04-11 DK DK153679A patent/DK153679A/da not_active IP Right Cessation
- 1979-04-12 DD DD79212191A patent/DD143551A5/de unknown
- 1979-04-12 ZA ZA791768A patent/ZA791768B/xx unknown
- 1979-04-12 CA CA000325808A patent/CA1120045A/fr not_active Expired
- 1979-04-13 HU HU79BA3772A patent/HU182451B/hu unknown
- 1979-04-13 JP JP4446679A patent/JPS54138563A/ja active Pending
- 1979-04-13 PL PL21488379A patent/PL214883A1/xx unknown
- 1979-04-17 AU AU46077/79A patent/AU4607779A/en not_active Abandoned

Also Published As

Publication number	Publication date
JPS54138563A (en)	1979-10-27
ZA791768B (en)	1980-05-28
HU182451B (en)	1984-01-30
IL57058A (en)	1983-06-15
EP0004895B1 (fr)	1981-04-01
IL57058A0 (en)	1979-07-25
EP0004895A3 (en)	1979-11-28
DE2816474A1 (de)	1979-10-25
DK153679A (da)	1979-10-16
ES479477A1 (es)	1979-07-16
US4250187A (en)	1981-02-10
EP0004895A2 (fr)	1979-10-31
BR7902212A (pt)	1979-12-04
DE2960227D1 (en)	1981-04-23
PL214883A1 (fr)	1980-01-28
CA1120045A (fr)	1982-03-16
PT69444A (de)	1979-05-01
AU4607779A (en)	1979-10-25

Publication	Publication Date	Title
DE2832698A1 (de)	1980-02-07	Substituierte 5-phenylcarbamoyl- barbitursaeuren, verfahren zu ihrer herstellung und ihre verwendung als insektizide
EP0017810B1 (fr)	1983-06-29	Agents pesticides contenant des benzazoles substitués et leur utilisation
EP0004022A1 (fr)	1979-09-19	Dérivés pentafluorobenzyloxycarbonylés, méthode de préparation et leur utilisation comme insecticides et acaricides
EP0043978B1 (fr)	1983-08-24	N-Phosphonyl-carbonyl carbamates, leur procédé de préparation, compositions pesticides contenant ces composés et leur utilisation comme pesticides
EP0043492B1 (fr)	1983-10-05	Esters d'acides 1-aryl-cyclopropan-1-carboxyliques, leur préparation et leur application comme insecticides
EP0004895B1 (fr)	1981-04-01	Dérivés de dichlorobenzodioxolanes, procédé pour leur préparation et leur utilisation comme agents synergétiques dans les insecticides et acaricides
EP0004902B1 (fr)	1982-04-21	Dérivés de benzodioxolanes, procédé pour leur préparation et leur utilisation comme synergistes de pesticides
EP0000537B1 (fr)	1980-12-10	Agents insecticides et acaricides, leur utilisation et procédés pour leur préparation
EP0029515B1 (fr)	1982-12-22	Benzylesters d'acide 2,2,3,3-tetraméthylpropanecarboxylique substitués par du fluor, procédé pour leur préparation et leur utilisation comme pesticides
DE3012642A1 (de)	1981-10-08	3-carbamoyl-4-hydroxy-cumarine, verfahren zu ihrer herstellung als schaedlingsbekaepfungsmittel
EP0001566B1 (fr)	1980-11-26	Dérivés d'acides cyclobutane carboxyliques, leurs procédés de préparation, et leur application comme insecticides
EP0004929B1 (fr)	1981-04-08	Agents insecticides et acaricides contenant des dérivés d'isochromane, leur procédé de fabrication et leur utilisation
EP0001424A1 (fr)	1979-04-18	Agents insecticides
DE2819932A1 (de)	1979-11-15	N,n-dimethyl-o-pyrazolyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide
EP0029160A1 (fr)	1981-05-27	Dérivés de l'oxybenzotriazole, procédé pour leur préparation et leur utilisation comme agents de synergie dans les préparations pesticides
US4199593A (en)	1980-04-22	Combating arthropods with 5-(3,4-methylenedioxybenzyl)-dioxolanes and synergistic compositions therewith
EP0029138B1 (fr)	1983-02-16	Agents pesticides contenant des 2-(thi)oxo-1,3,2-oxazaphospholanes et leur préparation
EP0028752A1 (fr)	1981-05-20	(Thi)oxo-2 oxaza-1,3-phospholane-2, procédé pour leur préparation et leur utilisation comme agents ayant un effet de synergie dans des pesticides
DE2836328A1 (de)	1980-02-28	N-(o-aethyl-s-n-propyl-(di)thiophosphoryloxy)-naphthalimide, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
DE2820360A1 (de)	1979-11-15	Neues n-carboxyliertes carbamat, verfahren zu seiner herstellung und seine insektizide verwendung
EP0044994A1 (fr)	1982-02-03	N-méthylcarbamates carboxylés, leur préparation et leur emploi comme pesticides
DE2806834A1 (de)	1979-08-23	Insektizide mittel
DE2701586A1 (de)	1978-07-20	Insektizide und akarizide mittel
EP0000895A1 (fr)	1979-03-07	Aryl-N-alkylcarbamates, leur procédé de préparation et leur application comme insecticides
DE2823281A1 (de)	1979-11-29	Insektizide und akarizide mittel