KR930005961A - 1-알콕시헥사트리엔-2-카복실레이트 - Google Patents
1-알콕시헥사트리엔-2-카복실레이트 Download PDFInfo
- Publication number
- KR930005961A KR930005961A KR1019920016392A KR920016392A KR930005961A KR 930005961 A KR930005961 A KR 930005961A KR 1019920016392 A KR1019920016392 A KR 1019920016392A KR 920016392 A KR920016392 A KR 920016392A KR 930005961 A KR930005961 A KR 930005961A
- Authority
- KR
- South Korea
- Prior art keywords
- methyl
- carboxylate
- methoxy
- straight
- case
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 5
- 238000000034 method Methods 0.000 claims abstract 2
- 239000000575 pesticide Substances 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 15
- -1 compound methyl 1-methoxy-3-methyl- 6- (4-methoxyphenyl) -hexatriene-2-carboxylate Chemical class 0.000 claims 13
- 125000001424 substituent group Chemical group 0.000 claims 10
- 125000000217 alkyl group Chemical group 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 6
- 125000005843 halogen group Chemical group 0.000 claims 6
- 150000002367 halogens Chemical class 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 125000003342 alkenyl group Chemical group 0.000 claims 4
- 125000003302 alkenyloxy group Chemical group 0.000 claims 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 4
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 4
- 125000000304 alkynyl group Chemical group 0.000 claims 4
- 125000005133 alkynyloxy group Chemical group 0.000 claims 4
- 125000004438 haloalkoxy group Chemical group 0.000 claims 4
- 125000001188 haloalkyl group Chemical group 0.000 claims 4
- YQRHZGOTQSHPNW-UHFFFAOYSA-N methyl 2-(methoxymethylidene)-3-methyl-6-[2-(3-methylbut-2-enoxy)phenyl]hexa-3,5-dienoate Chemical compound COC=C(C(=O)OC)C(C)=CC=CC1=CC=CC=C1OCC=C(C)C YQRHZGOTQSHPNW-UHFFFAOYSA-N 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 241000607479 Yersinia pestis Species 0.000 claims 3
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- RIGZIGSLGOTINN-UHFFFAOYSA-N methyl 2-(methoxymethylidene)-3-methyl-6-[3-(3-methylbut-2-enoxy)phenyl]hexa-3,5-dienoate Chemical compound COC=C(C(=O)OC)C(C)=CC=CC1=CC=CC(OCC=C(C)C)=C1 RIGZIGSLGOTINN-UHFFFAOYSA-N 0.000 claims 3
- MTTZSOSUZLNSSO-UHFFFAOYSA-N methyl 2-(methoxymethylidene)-6-(3-methoxyphenyl)-3-methylhexa-3,5-dienoate Chemical compound COC=C(C(=O)OC)C(C)=CC=CC1=CC=CC(OC)=C1 MTTZSOSUZLNSSO-UHFFFAOYSA-N 0.000 claims 3
- ZDIQYKMDNQULMX-UHFFFAOYSA-N methyl 6-(4-chloro-3-methoxyphenyl)-2-(methoxymethylidene)-3-methylhexa-3,5-dienoate Chemical compound COC=C(C(=O)OC)C(C)=CC=CC1=CC=C(Cl)C(OC)=C1 ZDIQYKMDNQULMX-UHFFFAOYSA-N 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 125000004666 alkoxyiminoalkyl group Chemical group 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/734—Ethers
-
- 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
- A01N49/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds containing the group, wherein m+n>=1, both X together may also mean —Y— or a direct carbon-to-carbon bond, and the carbon atoms marked with an asterisk are not part of any ring system other than that which may be formed by the atoms X, the carbon atoms in square brackets being part of any acyclic or cyclic structure, or the group, wherein A means a carbon atom or Y, n>=0, and not more than one of these carbon atoms being a member of the same ring system, e.g. juvenile insect hormones or mimics thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Insects & Arthropods (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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4129962A DE4129962A1 (de) | 1991-09-10 | 1991-09-10 | 1-alkoxyhexatrien-2-carbonsaeureester |
| DEP4129962.0 | 1991-09-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR930005961A true KR930005961A (ko) | 1993-04-20 |
Family
ID=6440214
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019920016392A Withdrawn KR930005961A (ko) | 1991-09-10 | 1992-09-08 | 1-알콕시헥사트리엔-2-카복실레이트 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5420160A (cg-RX-API-DMAC7.html) |
| EP (1) | EP0531821B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JPH05213822A (cg-RX-API-DMAC7.html) |
| KR (1) | KR930005961A (cg-RX-API-DMAC7.html) |
| BR (1) | BR9203501A (cg-RX-API-DMAC7.html) |
| DE (2) | DE4129962A1 (cg-RX-API-DMAC7.html) |
| TW (1) | TW202431B (cg-RX-API-DMAC7.html) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1287161B1 (it) * | 1996-11-14 | 1998-08-04 | Isagro Ricerca Srl | Composti analoghi delle strobilurine aventi attivita' fungicida |
| US7842727B2 (en) * | 2001-03-27 | 2010-11-30 | Errant Gene Therapeutics, Llc | Histone deacetylase inhibitors |
| US7312247B2 (en) * | 2001-03-27 | 2007-12-25 | Errant Gene Therapeutics, Llc | Histone deacetylase inhibitors |
| US8026280B2 (en) | 2001-03-27 | 2011-09-27 | Errant Gene Therapeutics, Llc | Histone deacetylase inhibitors |
| US6495719B2 (en) * | 2001-03-27 | 2002-12-17 | Circagen Pharmaceutical | Histone deacetylase inhibitors |
| EP1511477A4 (en) * | 2002-05-22 | 2008-04-09 | Errant Gene Therapeutics Llc | HISTONE DEACETYLASE INHIBITORS BASED ON ALPHA-KETO-EPOXYDE COMPOUNDS |
| JP2006508986A (ja) * | 2002-11-20 | 2006-03-16 | エルラント ゲネ セラペウチクス エルエルシー | ヒストンデアセチラーゼ阻害剤による肺細胞の治療方法 |
| CA2587013A1 (en) * | 2004-11-08 | 2006-05-18 | Errant Gene Therapeutics, Llc | Histone deacetylase inhibitors |
| FR2968652B1 (fr) | 2010-12-10 | 2015-06-26 | Snecma Propulsion Solide | Materiaux et pieces resistants a haute temperature en milieu oxydant et leur procede de fabrication |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4334696A (en) * | 1980-06-04 | 1982-06-15 | Ab Volvo | Rear wheel mounting for motor vehicles with a rigid rear axle |
| DE4014940A1 (de) * | 1989-09-01 | 1991-03-07 | Bayer Ag | Substituierte acrylsaeureester |
| DE4012792A1 (de) * | 1990-04-21 | 1991-10-24 | Bayer Ag | Verfahren zur herstellung von 1-alkoxyhexatrien-2-carbonsaeureestern |
-
1991
- 1991-09-10 DE DE4129962A patent/DE4129962A1/de not_active Withdrawn
-
1992
- 1992-08-14 TW TW081106426A patent/TW202431B/zh active
- 1992-08-28 DE DE59205221T patent/DE59205221D1/de not_active Expired - Fee Related
- 1992-08-28 EP EP92114683A patent/EP0531821B1/de not_active Expired - Lifetime
- 1992-09-03 JP JP4260694A patent/JPH05213822A/ja active Pending
- 1992-09-08 KR KR1019920016392A patent/KR930005961A/ko not_active Withdrawn
- 1992-09-09 BR BR929203501A patent/BR9203501A/pt not_active Application Discontinuation
-
1994
- 1994-01-21 US US08/184,732 patent/US5420160A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP0531821B1 (de) | 1996-01-31 |
| DE59205221D1 (de) | 1996-03-14 |
| DE4129962A1 (de) | 1993-03-11 |
| EP0531821A2 (de) | 1993-03-17 |
| US5420160A (en) | 1995-05-30 |
| TW202431B (cg-RX-API-DMAC7.html) | 1993-03-21 |
| JPH05213822A (ja) | 1993-08-24 |
| EP0531821A3 (en) | 1993-08-25 |
| BR9203501A (pt) | 1993-04-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR920014771A (ko) | 제초제 | |
| KR870011140A (ko) | 1,2,3,6-테트라하이드로-5-니트로니-피리미딘 유도체 | |
| KR910009157A (ko) | 제초성 조성물 | |
| KR910000754A (ko) | 티아졸로피리미딘 유도체, 이의 제조방법 및 이의 농약으로서의 용도 | |
| KR950000652A (ko) | 2-옥스이미노-2-페닐-아세트아미드 | |
| KR960012172B1 (ko) | 피라졸 유도체 및 이 유도체를 활성 성분으로 함유하는 살충제 및 살비제 조성물 | |
| KR940003934A (ko) | 피리딜옥시-아크릴산 에스테르 | |
| KR880002872A (ko) | 트리아졸로- 피리미딘-2-설폰아미드 | |
| KR900003161A (ko) | 치환된 디옥솔란, 이의 제조방법 및 살균제로서의 이의 용도 | |
| KR870007878A (ko) | 해충 방제에 유용한 벤조일페닐우레아 및 그의 제조방법 | |
| KR910006206A (ko) | 치환된 아크릴산 에스테르. | |
| KR930703269A (ko) | 술포닐우레아 유도체, 그의 제조 방법 및 용도 | |
| CA2480552A1 (en) | Amidoacetonitrile compounds and their use as pesticides | |
| KR930007918A (ko) | 신규한2-(2-벤족사졸릴-옥시)-아세트아미드 | |
| JP2002500222A5 (cg-RX-API-DMAC7.html) | ||
| US5420160A (en) | 1-alkoxyhexatriene-2-carboxylates | |
| KR880007489A (ko) | 치환된 4-아미노-피리미딘 및 이의 제조방법 | |
| KR930007934A (ko) | 피라졸린 | |
| KR880012550A (ko) | 헤테로사일클릭 네오판 동족체, 이의 제조 방법 및 해충 방제제로서의 이의 용도 | |
| KR890012965A (ko) | 헤테로사이클릭 라디칼에 의해 치환된 아크릴산 에스테르 | |
| EP0819115A1 (en) | Fungicidal compounds | |
| KR910011848A (ko) | 치환된 1-아미노메틸-3-아릴-4-시아노-피롤 | |
| KR900004255A (ko) | 2-할로게노알킬티오-치환된 피리미딘 유도체를 기본으로 하는 살충제 | |
| US4596801A (en) | 4H-3,1-benzoxazine derivatives, process for producing the same and agricultural or horticultural fungicide containing the same | |
| KR940000442A (ko) | 신규한 2-(7-클로로-2-벤족사졸릴옥시)-아세트아미드 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19920908 |
|
| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |