JP2017534732A5 - - Google Patents
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- Publication number
- JP2017534732A5 JP2017534732A5 JP2017525060A JP2017525060A JP2017534732A5 JP 2017534732 A5 JP2017534732 A5 JP 2017534732A5 JP 2017525060 A JP2017525060 A JP 2017525060A JP 2017525060 A JP2017525060 A JP 2017525060A JP 2017534732 A5 JP2017534732 A5 JP 2017534732A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- fragrance
- compound represented
- cycloalkyl
- alkenyl
- 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.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims 10
- 239000003205 fragrance Substances 0.000 claims 9
- 125000003342 alkenyl group Chemical group 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- 229920006395 saturated elastomer Polymers 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 5
- 239000002304 perfume Substances 0.000 claims 4
- -1 4- (tert-butyl) phenyl Chemical group 0.000 claims 3
- IOHPVZBSOKLVMN-UHFFFAOYSA-N 2-(2-phenylethyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1CCC1=CC=CC=C1 IOHPVZBSOKLVMN-UHFFFAOYSA-N 0.000 claims 2
- 241000234269 Liliales Species 0.000 claims 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical class CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 claims 2
- 150000001299 aldehydes Chemical group 0.000 claims 2
- 239000000796 flavoring agent Substances 0.000 claims 2
- 235000019634 flavors Nutrition 0.000 claims 2
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- NTXNPSABDJRPGF-UHFFFAOYSA-N 3-(4-tert-butyl-2-methylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1C NTXNPSABDJRPGF-UHFFFAOYSA-N 0.000 claims 1
- UKZXPOJABTXLMK-UHFFFAOYSA-N 3-[2-methyl-4-(2-methylpropyl)phenyl]propanal Chemical compound CC(C)CC1=CC=C(CCC=O)C(C)=C1 UKZXPOJABTXLMK-UHFFFAOYSA-N 0.000 claims 1
- RCQMMCWUKHWWDZ-UHFFFAOYSA-N 4-(4-propan-2-ylphenyl)butanal Chemical compound CC(C)C1=CC=C(CCCC=O)C=C1 RCQMMCWUKHWWDZ-UHFFFAOYSA-N 0.000 claims 1
- DKKMZZPXYXGUQH-UHFFFAOYSA-N 4-(4-tert-butylphenyl)butanal Chemical compound CC(C)(C)C1=CC=C(CCCC=O)C=C1 DKKMZZPXYXGUQH-UHFFFAOYSA-N 0.000 claims 1
- NRCLUAUOPXATRW-UHFFFAOYSA-N 4-[4-(2-methylpropyl)phenyl]butanal Chemical compound CC(C)CC1=CC=C(CCCC=O)C=C1 NRCLUAUOPXATRW-UHFFFAOYSA-N 0.000 claims 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims 1
- 241000700159 Rattus Species 0.000 claims 1
- 150000007854 aminals Chemical class 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 230000015556 catabolic process Effects 0.000 claims 1
- 238000006731 degradation reaction Methods 0.000 claims 1
- 150000002081 enamines Chemical class 0.000 claims 1
- 210000003494 hepatocyte Anatomy 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- 230000035945 sensitivity Effects 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/EP2014/074179 WO2016074697A1 (en) | 2014-11-10 | 2014-11-10 | Improvements in or relating to organic compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017534732A JP2017534732A (ja) | 2017-11-24 |
| JP2017534732A5 true JP2017534732A5 (OSRAM) | 2018-01-11 |
| JP6479980B2 JP6479980B2 (ja) | 2019-03-06 |
Family
ID=51871046
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017525060A Active JP6479980B2 (ja) | 2014-11-10 | 2014-11-10 | 有機化合物におけるまたは関連する改善 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20180230399A1 (OSRAM) |
| EP (1) | EP3218459B1 (OSRAM) |
| JP (1) | JP6479980B2 (OSRAM) |
| CN (1) | CN107074712B (OSRAM) |
| BR (1) | BR112017007005B1 (OSRAM) |
| CO (1) | CO2017005642A2 (OSRAM) |
| MX (1) | MX2017004871A (OSRAM) |
| RU (1) | RU2669029C1 (OSRAM) |
| SG (1) | SG11201702973RA (OSRAM) |
| WO (1) | WO2016074697A1 (OSRAM) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2546519A (en) * | 2016-01-21 | 2017-07-26 | Givaudan Sa | Improvements in or relating to organic compounds |
| US11104688B2 (en) | 2017-10-04 | 2021-08-31 | Henkel Ag & Co. Kgaa | Pro-fragrances and method of preparation thereof |
| WO2019122236A1 (en) | 2017-12-21 | 2019-06-27 | Firmenich Sa | Method for identifying positive allosteric modulators for odorant receptors |
| EP3853328A2 (en) | 2018-12-19 | 2021-07-28 | Firmenich SA | Use of volatile compounds to modulate the perception of floral muguet |
| GB201909221D0 (en) | 2019-06-27 | 2019-08-14 | Givaudan Sa | Improvements in or relating to organic compounds |
| EP4046985B1 (en) | 2019-10-17 | 2023-11-01 | Mitsubishi Gas Chemical Company, Inc. | Aldehyde compound and method for producing same, and fragrance composition |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7502553A (en) * | 1975-02-13 | 1976-08-17 | Ruhrchemie Ag | Hydroformylated tert. butyl- and isopropyl allyl benzenes - useful aromatizing cpds |
| JPS6485978A (en) * | 1987-06-09 | 1989-03-30 | Yoshitomi Pharmaceutical | Novel thienodiazepine derivative |
| US4837201A (en) * | 1988-05-17 | 1989-06-06 | Basf Aktiengesellschaft | 4-Methyl-4-phenyl-1-pentanals, their preparation and their use as scents |
| US4910346A (en) * | 1988-11-10 | 1990-03-20 | Givaudan Corporation | 3-(3-propan-2-ylphenyl)butanal and 3-(3-propen-2-ylphenyl)butanal |
| DE3933781A1 (de) * | 1989-10-10 | 1991-04-18 | Boehringer Ingelheim Kg | Verfahren zur herstellung von 4-(4-isobutylphenyl)-butyraldehyd |
| CH689372A5 (fr) * | 1995-03-03 | 1999-03-31 | Firmenich & Cie | Aldéhyde aralkylique et son utilisation en tant qu'ingrédient parfumant. |
| US6083901A (en) * | 1998-08-28 | 2000-07-04 | General Electric Company | Emulsions of fragrance releasing silicon compounds |
| KR100621823B1 (ko) * | 2004-07-21 | 2006-09-14 | 재단법인서울대학교산학협력재단 | 2,6-디알킬테트랄린의 제조 방법 |
| FR2880883B1 (fr) * | 2005-01-19 | 2009-01-09 | Mane Fils Sa V | Nouveaux derives de trimethylcyclododecatriene, leur utilisation et produits parfumes les contenant |
| GB0611770D0 (en) * | 2006-06-15 | 2006-07-26 | Givaudan Sa | Compounds |
| EP2233556A1 (en) * | 2009-03-23 | 2010-09-29 | O'Laughlin Industries, Co. Ltd. | Isomeric mixture of meta and para tertio-butylphenyl propanal and production thereof |
| WO2011127933A1 (en) * | 2010-04-16 | 2011-10-20 | Nuevolution A/S | Bi-functional complexes and methods for making and using such complexes |
| CN103874755B (zh) * | 2011-09-30 | 2016-08-17 | 弗门尼舍有限公司 | 花香加香组合物 |
| DE102012201422A1 (de) * | 2012-02-01 | 2013-08-01 | Henkel Ag & Co. Kgaa | Kombination aus Aminoalkohol, Duftstoff und Kieselsäureester und ihre Verwendung als Duftstoffvorläufer |
-
2014
- 2014-11-10 BR BR112017007005-7A patent/BR112017007005B1/pt active IP Right Grant
- 2014-11-10 SG SG11201702973RA patent/SG11201702973RA/en unknown
- 2014-11-10 WO PCT/EP2014/074179 patent/WO2016074697A1/en not_active Ceased
- 2014-11-10 RU RU2017113156A patent/RU2669029C1/ru active
- 2014-11-10 MX MX2017004871A patent/MX2017004871A/es unknown
- 2014-11-10 US US15/516,238 patent/US20180230399A1/en not_active Abandoned
- 2014-11-10 JP JP2017525060A patent/JP6479980B2/ja active Active
- 2014-11-10 CN CN201480083185.5A patent/CN107074712B/zh active Active
- 2014-11-10 EP EP14796099.1A patent/EP3218459B1/en active Active
-
2017
- 2017-06-07 CO CONC2017/0005642A patent/CO2017005642A2/es unknown
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