NO791113L - Nye benzodioksolderivater. - Google Patents
Nye benzodioksolderivater.Info
- Publication number
- NO791113L NO791113L NO791113A NO791113A NO791113L NO 791113 L NO791113 L NO 791113L NO 791113 A NO791113 A NO 791113A NO 791113 A NO791113 A NO 791113A NO 791113 L NO791113 L NO 791113L
- Authority
- NO
- Norway
- Prior art keywords
- spp
- formula
- methyl
- alkyl
- chloro
- Prior art date
Links
- 239000013543 active substance Substances 0.000 claims description 25
- 150000005528 benzodioxoles Chemical class 0.000 claims description 24
- 229910052736 halogen Inorganic materials 0.000 claims description 19
- 150000002367 halogens Chemical class 0.000 claims description 19
- 239000001257 hydrogen Substances 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims description 11
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 150000001733 carboxylic acid esters Chemical class 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 8
- 230000000895 acaricidal effect Effects 0.000 claims description 6
- 150000001350 alkyl halides Chemical class 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 230000000749 insecticidal effect Effects 0.000 claims description 4
- FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical class C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 claims description 3
- 241000239223 Arachnida Species 0.000 claims description 3
- 241000238631 Hexapoda Species 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- 239000002917 insecticide Substances 0.000 claims 2
- 239000000642 acaricide Substances 0.000 claims 1
- -1 e.g. 2 Chemical class 0.000 description 30
- 125000000217 alkyl group Chemical group 0.000 description 23
- 239000000203 mixture Substances 0.000 description 20
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 13
- 239000002904 solvent Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 8
- 239000000460 chlorine Substances 0.000 description 8
- 229910052801 chlorine Inorganic materials 0.000 description 8
- 150000002825 nitriles Chemical class 0.000 description 8
- 230000002195 synergetic effect Effects 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 6
- 229910052794 bromium Inorganic materials 0.000 description 6
- TVRVRQOJFTXZNH-UHFFFAOYSA-N 2-(chloromethyl)-1,3-benzodioxole Chemical class C1=CC=C2OC(CCl)OC2=C1 TVRVRQOJFTXZNH-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 239000012074 organic phase Substances 0.000 description 5
- 150000002923 oximes Chemical class 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 238000009835 boiling Methods 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 125000000623 heterocyclic group Chemical group 0.000 description 4
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 241000607479 Yersinia pestis Species 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
- 125000004414 alkyl thio 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
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 3
- 125000004663 dialkyl amino group Chemical group 0.000 description 3
- 235000013312 flour Nutrition 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- 125000001188 haloalkyl group Chemical group 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 2
- CSXOGACWYJFTLV-UHFFFAOYSA-N 4-methyl-5-propyl-1,3-benzodioxole Chemical compound CCCC1=CC=C2OCOC2=C1C CSXOGACWYJFTLV-UHFFFAOYSA-N 0.000 description 2
- 241001143309 Acanthoscelides obtectus Species 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- 241000258937 Hemiptera Species 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-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
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-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
- 241001481703 Rhipicephalus <genus> Species 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 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
- 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 description 2
- JPOXNPPZZKNXOV-UHFFFAOYSA-N bromochloromethane Chemical compound ClCBr JPOXNPPZZKNXOV-UHFFFAOYSA-N 0.000 description 2
- 244000309464 bull Species 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 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
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 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
- 230000001804 emulsifying effect Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- 238000003197 gene knockdown Methods 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 230000002140 halogenating effect Effects 0.000 description 2
- 239000004312 hexamethylene tetramine Substances 0.000 description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate Chemical compound [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 229960005235 piperonyl butoxide Drugs 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000047 product Substances 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
- 239000004575 stone Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 2
- 125000004953 trihalomethyl group Chemical group 0.000 description 2
- 238000005292 vacuum distillation Methods 0.000 description 2
- RAZPNOWBVGAAAX-UHFFFAOYSA-N (4,6-dichloro-1,3-benzodioxol-5-yl)methyl acetate Chemical compound CC(=O)OCC1=C(Cl)C=C2OCOC2=C1Cl RAZPNOWBVGAAAX-UHFFFAOYSA-N 0.000 description 1
- IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 description 1
- 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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- 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
- BWBIFYYKIWPTRV-UHFFFAOYSA-N 2,2-dimethyl-1,3-benzodioxole Chemical compound C1=CC=C2OC(C)(C)OC2=C1 BWBIFYYKIWPTRV-UHFFFAOYSA-N 0.000 description 1
- OJJBVZVMDFHIHB-UHFFFAOYSA-N 2-(1,3-benzodioxol-2-yl)-3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical compound C1(C2C(C(N1C1OC3=C(O1)C=CC=C3)=O)CCC=C2)=O OJJBVZVMDFHIHB-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- C07D317/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782816190 DE2816190A1 (de) | 1978-04-14 | 1978-04-14 | Neue benzodioxolderivate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO791113L true NO791113L (no) | 1979-10-16 |
Family
ID=6036963
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO791113A NO791113L (no) | 1978-04-14 | 1979-04-03 | Nye benzodioksolderivater. |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US4427666A (tr) |
| EP (1) | EP0004902B1 (tr) |
| JP (1) | JPS54138562A (tr) |
| AR (1) | AR220555A1 (tr) |
| AT (1) | AT366884B (tr) |
| AU (1) | AU522902B2 (tr) |
| BR (1) | BR7902211A (tr) |
| CA (1) | CA1135709A (tr) |
| DD (1) | DD143550A5 (tr) |
| DE (2) | DE2816190A1 (tr) |
| DK (1) | DK153979A (tr) |
| EG (1) | EG13676A (tr) |
| ES (5) | ES479472A1 (tr) |
| FI (1) | FI791210A (tr) |
| GR (1) | GR71693B (tr) |
| HU (1) | HU182450B (tr) |
| IL (1) | IL57057A0 (tr) |
| JO (1) | JO998B1 (tr) |
| LU (1) | LU81149A1 (tr) |
| NO (1) | NO791113L (tr) |
| NZ (1) | NZ190161A (tr) |
| OA (1) | OA06234A (tr) |
| PH (1) | PH14741A (tr) |
| PL (1) | PL214856A1 (tr) |
| PT (1) | PT69443A (tr) |
| TR (1) | TR19874A (tr) |
| ZA (1) | ZA791765B (tr) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4965254A (en) * | 1985-02-14 | 1990-10-23 | Bayer Aktiengesellschaft | Agents for combating pests |
| US4732906A (en) * | 1985-04-08 | 1988-03-22 | Chugai Seiyaki Kabushiki Kaisha | Dioxolobenzizoxazole derivatives |
| FI874163A (fi) * | 1986-09-26 | 1988-03-27 | Mitsui Toatsu Chemicals | Katekolderivat samt preparat innehaollande desamma foer haemmande och botande av regressiva sjukdomar i det centrala nervsystemet. |
| FR2609989B1 (fr) * | 1987-01-28 | 1989-04-14 | Rhone Poulenc Chimie | Procede de preparation de methoxy-3 methylenedioxy-4,5 benzaldehyde |
| GB9112697D0 (en) * | 1991-06-13 | 1991-07-31 | Shell Int Research | Biocidal compounds |
| DK174168B1 (da) | 1999-07-19 | 2002-08-05 | Hardi Int As | Bomkonstruktion, samt drejeled til en bomkonstruktion |
| JP2003534340A (ja) * | 2000-05-24 | 2003-11-18 | スミスクライン・ビーチャム・コーポレイション | 脂肪酸シンターゼ阻害剤 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2734908A (en) | 1956-02-14 | Method of producing aralkyl cyanides | ||
| US2878265A (en) | 1956-09-10 | 1959-03-17 | Fmc Corp | Production of methylenedioxyphenyl derivatives |
| DE1154810B (de) | 1961-04-01 | 1963-09-26 | Knoll Ag | Verfahren zur Herstellung basisch substituierter Phenylacetonitrile |
| GB1046209A (en) | 1964-07-24 | 1966-10-19 | Shell Int Research | Insecticidal compositions |
| DE1543609A1 (de) | 1966-08-13 | 1969-09-18 | Hoechst Ag | Substituierte Phenylessigsaeureamide und Verfahren zu ihrer Herstellung |
| GB1542641A (en) * | 1975-06-30 | 1979-03-21 | Shell Int Research | Wild oat herbicide |
| US4182771A (en) | 1976-12-01 | 1980-01-08 | Bayer Aktiengesellschaft | Synergistic arthropodicidal compositions containing α-substituted-3,4-methylenedioxyph-enylacetonitriles |
| DE2734108A1 (de) | 1977-07-28 | 1979-02-08 | Bayer Ag | Insektizide und akarizide mittel |
-
1978
- 1978-04-14 DE DE19782816190 patent/DE2816190A1/de not_active Withdrawn
-
1979
- 1979-03-22 JO JO1979998A patent/JO998B1/en active
- 1979-04-03 NO NO791113A patent/NO791113L/no unknown
- 1979-04-04 EP EP79101016A patent/EP0004902B1/de not_active Expired
- 1979-04-04 DE DE7979101016T patent/DE2962540D1/de not_active Expired
- 1979-04-06 PT PT69443A patent/PT69443A/pt unknown
- 1979-04-06 GR GR58825A patent/GR71693B/el unknown
- 1979-04-10 DD DD79212119A patent/DD143550A5/de unknown
- 1979-04-10 PH PH22375A patent/PH14741A/en unknown
- 1979-04-10 ES ES479472A patent/ES479472A1/es not_active Expired
- 1979-04-10 BR BR7902211A patent/BR7902211A/pt unknown
- 1979-04-11 EG EG218/79A patent/EG13676A/xx active
- 1979-04-11 AR AR276156A patent/AR220555A1/es active
- 1979-04-11 DK DK153979A patent/DK153979A/da unknown
- 1979-04-11 IL IL57057A patent/IL57057A0/xx unknown
- 1979-04-11 NZ NZ190161A patent/NZ190161A/xx unknown
- 1979-04-12 ZA ZA791765A patent/ZA791765B/xx unknown
- 1979-04-12 TR TR19874A patent/TR19874A/tr unknown
- 1979-04-12 PL PL21485679A patent/PL214856A1/xx unknown
- 1979-04-12 JP JP4368779A patent/JPS54138562A/ja active Pending
- 1979-04-12 FI FI791210A patent/FI791210A/fi not_active Application Discontinuation
- 1979-04-12 CA CA000325805A patent/CA1135709A/en not_active Expired
- 1979-04-12 OA OA56785A patent/OA06234A/xx unknown
- 1979-04-13 LU LU81149A patent/LU81149A1/de unknown
- 1979-04-13 HU HU79BA3771A patent/HU182450B/hu unknown
- 1979-04-13 AT AT0279979A patent/AT366884B/de active
- 1979-04-17 AU AU46078/79A patent/AU522902B2/en not_active Ceased
- 1979-09-13 ES ES484151A patent/ES484151A1/es not_active Expired
- 1979-09-13 ES ES484153A patent/ES484153A1/es not_active Expired
- 1979-09-13 ES ES484152A patent/ES484152A1/es not_active Expired
- 1979-09-13 ES ES484154A patent/ES484154A1/es not_active Expired
-
1982
- 1982-06-15 US US06/388,566 patent/US4427666A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| FI791210A (fi) | 1979-10-15 |
| EP0004902A2 (de) | 1979-10-31 |
| ATA279979A (de) | 1981-10-15 |
| AU522902B2 (en) | 1982-07-01 |
| TR19874A (tr) | 1980-04-03 |
| HU182450B (en) | 1984-01-30 |
| PH14741A (en) | 1981-11-20 |
| EG13676A (en) | 1982-03-31 |
| OA06234A (fr) | 1981-06-30 |
| DK153979A (da) | 1979-10-15 |
| ES484154A1 (es) | 1980-05-16 |
| NZ190161A (en) | 1981-01-23 |
| JO998B1 (en) | 1982-07-10 |
| DE2816190A1 (de) | 1979-10-25 |
| PL214856A1 (tr) | 1980-03-24 |
| DE2962540D1 (en) | 1982-06-03 |
| ES484152A1 (es) | 1980-05-16 |
| LU81149A1 (de) | 1979-11-07 |
| DD143550A5 (de) | 1980-09-03 |
| EP0004902B1 (de) | 1982-04-21 |
| EP0004902A3 (en) | 1979-11-28 |
| AU4607879A (en) | 1979-10-18 |
| AR220555A1 (es) | 1980-11-14 |
| CA1135709A (en) | 1982-11-16 |
| JPS54138562A (en) | 1979-10-27 |
| IL57057A0 (en) | 1979-07-25 |
| AT366884B (de) | 1982-05-10 |
| BR7902211A (pt) | 1979-12-04 |
| GR71693B (tr) | 1983-06-21 |
| ES484151A1 (es) | 1980-05-16 |
| ES484153A1 (es) | 1980-05-16 |
| PT69443A (en) | 1979-05-01 |
| ES479472A1 (es) | 1979-12-01 |
| ZA791765B (en) | 1980-05-28 |
| US4427666A (en) | 1984-01-24 |
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