JPWO2019243501A5 - - Google Patents
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- JPWO2019243501A5 JPWO2019243501A5 JP2020550628A JP2020550628A JPWO2019243501A5 JP WO2019243501 A5 JPWO2019243501 A5 JP WO2019243501A5 JP 2020550628 A JP2020550628 A JP 2020550628A JP 2020550628 A JP2020550628 A JP 2020550628A JP WO2019243501 A5 JPWO2019243501 A5 JP WO2019243501A5
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- benzene
- alkyl group
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- 150000001875 compounds Chemical class 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 14
- 239000002304 perfume Substances 0.000 claims description 6
- 230000002708 enhancing effect Effects 0.000 claims description 4
- 239000004744 fabric Substances 0.000 claims description 4
- 239000000047 product Substances 0.000 claims 21
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 6
- -1 Formic acid ester Chemical class 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 5
- 239000003570 air Substances 0.000 claims 4
- 125000002723 alicyclic group Chemical group 0.000 claims 4
- 229920006395 saturated elastomer Polymers 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- 150000001299 aldehydes Chemical class 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 239000004615 ingredient Substances 0.000 claims 3
- 150000002576 ketones Chemical class 0.000 claims 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims 3
- 239000002243 precursor Substances 0.000 claims 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 239000002386 air freshener Substances 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 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
- 125000001033 ether group Chemical group 0.000 claims 2
- 239000003205 fragrance Substances 0.000 claims 2
- 150000002430 hydrocarbons Chemical group 0.000 claims 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- ANNQZEWMSAKQLX-UHFFFAOYSA-N 1-(2-cyclohexylethoxy)prop-1-en-2-ylbenzene Chemical compound C1(CCCCC1)CCOC=C(C)C1=CC=CC=C1 ANNQZEWMSAKQLX-UHFFFAOYSA-N 0.000 claims 1
- NXNOKHHFNPXZIQ-UHFFFAOYSA-N 1-(2-cyclohexyloxyethenyl)-4-methoxybenzene Chemical compound C1(CCCCC1)OC=CC1=CC=C(C=C1)OC NXNOKHHFNPXZIQ-UHFFFAOYSA-N 0.000 claims 1
- JEZGFKAFCJPYGQ-UHFFFAOYSA-N 1-(3-methylbutoxy)prop-1-en-2-ylbenzene Chemical compound C(CC(C)C)OC=C(C)C1=CC=CC=C1 JEZGFKAFCJPYGQ-UHFFFAOYSA-N 0.000 claims 1
- YOOGLOFAYIEKNN-UHFFFAOYSA-N 1-dodecoxyprop-1-en-2-ylbenzene Chemical compound CCCCCCCCCCCCOC=C(C)C1=CC=CC=C1 YOOGLOFAYIEKNN-UHFFFAOYSA-N 0.000 claims 1
- FCTGEMDIBOJIOF-UHFFFAOYSA-N 1-ethenyl-2-pentoxybenzene Chemical compound CCCCCOC1=CC=CC=C1C=C FCTGEMDIBOJIOF-UHFFFAOYSA-N 0.000 claims 1
- KYKAAGKOJILMOP-UHFFFAOYSA-N 1-methyl-4-[1-(2-phenylcyclohexyl)oxyprop-1-en-2-yl]benzene Chemical compound CC1=CC=C(C=C1)C(=COC1C(CCCC1)C1=CC=CC=C1)C KYKAAGKOJILMOP-UHFFFAOYSA-N 0.000 claims 1
- MLZJXXWYCMCTNF-UHFFFAOYSA-N 2-(3-methylbut-2-enoxy)ethenylbenzene Chemical compound CC(C)=CCOC=CC1=CC=CC=C1 MLZJXXWYCMCTNF-UHFFFAOYSA-N 0.000 claims 1
- CDYLRVAKRZDURI-UHFFFAOYSA-N 2-cyclohexyloxyethenylbenzene Chemical compound C1CCCCC1OC=CC1=CC=CC=C1 CDYLRVAKRZDURI-UHFFFAOYSA-N 0.000 claims 1
- ZMMNCXVXTAFGBC-UHFFFAOYSA-N 2-heptoxyethenylbenzene Chemical compound CCCCCCCOC=CC1=CC=CC=C1 ZMMNCXVXTAFGBC-UHFFFAOYSA-N 0.000 claims 1
- OYZWFFFNQPNZRD-UHFFFAOYSA-N 2-hexoxyethenylbenzene Chemical compound CCCCCCOC=CC1=CC=CC=C1 OYZWFFFNQPNZRD-UHFFFAOYSA-N 0.000 claims 1
- 241000195940 Bryophyta Species 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 claims 1
- 206010042496 Sunburn Diseases 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 239000012080 ambient air Substances 0.000 claims 1
- 230000001166 anti-perspirative effect Effects 0.000 claims 1
- 239000003213 antiperspirant Substances 0.000 claims 1
- 239000007844 bleaching agent Substances 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 239000002537 cosmetic Substances 0.000 claims 1
- 239000006071 cream Substances 0.000 claims 1
- 125000006165 cyclic alkyl group Chemical group 0.000 claims 1
- 239000002781 deodorant agent Substances 0.000 claims 1
- 239000000645 desinfectant Substances 0.000 claims 1
- 239000003599 detergent Substances 0.000 claims 1
- 238000009792 diffusion process Methods 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 239000002979 fabric softener Substances 0.000 claims 1
- 235000019253 formic acid Nutrition 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 239000000499 gel Substances 0.000 claims 1
- 239000000118 hair dye Substances 0.000 claims 1
- 239000008266 hair spray Substances 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 238000010409 ironing Methods 0.000 claims 1
- 239000010985 leather Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000006210 lotion Substances 0.000 claims 1
- 235000011929 mousse Nutrition 0.000 claims 1
- 239000003921 oil Substances 0.000 claims 1
- 239000000123 paper Substances 0.000 claims 1
- 239000002453 shampoo Substances 0.000 claims 1
- 238000007493 shaping process Methods 0.000 claims 1
- 239000000344 soap Substances 0.000 claims 1
- 239000013042 solid detergent Substances 0.000 claims 1
- 125000005504 styryl group Chemical group 0.000 claims 1
- 230000000475 sunscreen effect Effects 0.000 claims 1
- 239000000516 sunscreening agent Substances 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Description
本発明の他の目的は、前記で定義した式(I)の少なくとも1つの化合物を有効量で組成物又は物品に付加する、又は前記で定義した式(I)の少なくとも1つの化合物の有効量で表面に接触させる又は処理することを含む、付香組成物、付香組成物を取り巻く空気、表面又は着香物品のにおい特性を付与、増強、改善又は改変するための方法又はプロセスである。本明細書において使用される「表面」という用語は、式(I)の少なくとも1つの化合物を含む又は含有する香料組成物を適用する、使用者の皮膚、毛髪、織物、又は硬質表面を示してよい。 Another object of the invention is to add to a composition or article an effective amount of at least one compound of formula (I) as defined above , or an effective amount of at least one compound of formula (I) as defined above. a method or process for imparting, enhancing, improving or modifying the odor characteristics of a scented composition, the air surrounding the scented composition, a surface or a scented article , including contacting or treating a surface with a scented composition. . The term "surface" as used herein refers to the user's skin, hair, fabric, or hard surface to which a perfume composition comprising or containing at least one compound of formula (I) is applied. good.
一実施形態において、本発明は、前記で定義した式(I)の少なくとも1つの化合物を有効量で組成物又は物品に付加する、又は前記で定義した式(I)の少なくとも1つの化合物の有効量で表面に接触させる又は処理することを含む、付香組成物、付香組成物を取り巻く空気、表面又は着香物品のにおい特性を付与、増強、改善又は改変するための前記した式(I)の少なくとも1つの化合物の使用にも関する。本明細書において使用される「表面」という用語は、式(I)の少なくとも1つの化合物を含む又は含有する香料組成物を適用する、使用者の皮膚、毛髪、織物、又は硬質表面を示してよい。 In one embodiment, the present invention provides for adding an effective amount of at least one compound of formula (I) as defined above to a composition or article, or providing an effective amount of at least one compound of formula (I) as defined above. Formulas as described above for imparting, enhancing, improving or modifying the odor characteristics of a perfuming composition, the air surrounding the perfuming composition, a surface or a perfumed article , including contacting or treating a surface with an amount ( It also relates to the use of at least one compound of I). The term "surface" as used herein refers to the user's skin, hair, fabric, or hard surface to which a perfume composition comprising or containing at least one compound of formula (I) is applied. good.
Claims (15)
a)式(II)のケトン又はアルデヒド
R1は、同時に又は独立して、芳香族環の少なくとも1つの置換基を示し、かつヒドロキシル基、C1-6アルキル基、C1-6アルコキシ基又はRCOO基、ROCO基(Rは水素原子又はC1-4アルキル基である)であり、又は2つの隣接するR1は、一緒の場合に、-O-(CH2)m-O-(mは1又は2である)を示すか、又は1つもしくは1超のヒドロキシル基、1つもしくは1超のC1-3アルキル基及び/又は1つもしくは1超のC1-3アルコキシ基によって任意に置換されているC5-10の飽和環もしくは不飽和環を形成し、
R2は、水素原子、C1-6アルキル基、又はヒドロキシル基、C1-3アルキル基、C1-3アルコキシ基、RCOOもしくはROCO基(Rは、互いに独立して、水素原子又はC1-4アルキル基である)によって任意に置換されているC6-10芳香族基を示す]、
b)式(III)のギ酸エステル
c)式(IV)のアルコール
からなる群から選択される化合物を、式(I)の前駆化合物を、触媒の非存在下で周囲条件に曝すことによって、前駆化合物から放出するための方法であって、前駆化合物が、式(I)
前記周囲条件が、室温、周囲空気、大気圧であることを含む、前記方法。 below,
a) Ketone or aldehyde of formula (II)
R 1 simultaneously or independently represents at least one substituent on an aromatic ring, and represents a hydroxyl group, a C 1-6 alkyl group, a C 1-6 alkoxy group, an RCOO group, a ROCO group (R is a hydrogen atom) or C 1-4 alkyl group), or two adjacent R 1s , when taken together, represent -O-(CH 2 ) m -O- (m is 1 or 2) or C 5-10 optionally substituted by one or more hydroxyl groups, one or more C 1-3 alkyl groups and/or one or more C 1-3 alkoxy groups forming a saturated or unsaturated ring,
R 2 is a hydrogen atom, a C 1-6 alkyl group, a hydroxyl group, a C 1-3 alkyl group, a C 1-3 alkoxy group, an RCOO or ROCO group (R is independently a hydrogen atom or a C 1 -4 alkyl group],
b) Formic acid ester of formula (III)
A method for releasing a compound selected from the group consisting of formula (I) from a precursor compound by exposing the precursor compound to ambient conditions in the absence of a catalyst , the precursor compound having the formula (I) I)
The method , wherein the ambient conditions include room temperature, ambient air, and atmospheric pressure .
RR 11 は、同時に又は独立して、芳香族環の少なくとも1つの置換基を示し、かつヒドロキシル基、Crepresents, simultaneously or independently, at least one substituent on the aromatic ring, and a hydroxyl group, C 1-61-6 アルキル基、CAlkyl group, C 1-61-6 アルコキシ基又はRCOO基、ROCO基[式中、Rは水素原子又はCAlkoxy group, RCOO group, ROCO group [wherein R is a hydrogen atom or C 1-41-4 アルキル基である]であり;又は2つの隣接するRis an alkyl group; or two adjacent R 11 は、一緒の場合に、-O-(CHWhen together, -O-(CH 22 )) mm -O-[式中、mは1又は2である]を示し、又は任意に1つ又は1超のヒドロキシル基、1つ又は1超のC-O-, where m is 1 or 2, or optionally one or more hydroxyl groups, one or more C 1-31-3 アルキル基及び/又は1つ又は1超のCAlkyl group and/or one or more C 1-31-3 アルコキシ基によって置換されたC C substituted by alkoxy group 5-105-10 飽和又は不飽和環を形成し、forming a saturated or unsaturated ring,
RR 22 は、Cis C 1-61-6 アルキル基を示し、Indicates an alkyl group,
RR 33 は、Cis C 4-104-10 直鎖、分枝鎖又は環状のアルキル基、アルケニル基又はアルカジエニル基、ベンジル基、又はヒドロキシル基、CStraight chain, branched chain or cyclic alkyl group, alkenyl group or alkadienyl group, benzyl group or hydroxyl group, C 1-31-3 アルキル基又はCAlkyl group or C 1-31-3 アルコキシ基によって任意に置換されるCC optionally substituted by an alkoxy group 7-167-16 アリールアルキル基、フェノキシメチル基、又はエーテル官能基を任意に含むCC optionally containing an arylalkyl group, phenoxymethyl group, or ether functionality 8-158-15 飽和又は不飽和脂環式基を示し、represents a saturated or unsaturated alicyclic group,
RR 4Four 及びRand R 5Five は、同時に又は独立して、水素原子、又はCare simultaneously or independently hydrogen atoms, or C 1-61-6 アルキル基又はCAlkyl group or C 2-62-6 アルケニル基を示し、又はRrepresents an alkenyl group, or R 33 及びRand R 4Four は、一緒の場合に、Care the same, C 5-125-12 直鎖又は分枝鎖のアルカンジイル基又はアルケンジイル基、又はCStraight chain or branched alkanediyl group or alkenediyl group, or C 5-125-12 脂環式基を示す]の化合物であって、a compound representing an alicyclic group,
(2-((3-メチルブテ-2-エン-1-イル)オキシ)ビニル)ベンゼン、(1-(イソペンチルオキシ)プロペ-1-エン-2-イル)ベンゼン、(2-(ペンチルオキシ)ビニル)ベンゼン、(1-(ドデシルオキシ)プロペ-1-エン-2-イル)ベンゼン、(2-(ヘキシルオキシ)ビニル)ベンゼン、(2-(ヘプチルオキシ)ビニル)ベンゼン、(2-(オクチルオキシ)ビニル)ベンゼン、(1-(2-シクロヘキシルエトキシ)プロペ-1-エン-2-イル)ベンゼン、2-(3,7-ジメチルオクタ-2,6-ジエン-1-イル)オキシ)ビニル)ベンゼン、(2-フェネトキシビニル)ベンゼン、(2-(シクロヘキシルオキシ)ビニル)ベンゼン、1-(2-(シクロヘキシルオキシ)ビニル)-4-メトキシベンゼン、(1-(2-シクロヘキシルエトキシ)プロペ-1-エン-2-イル)ベンゼン及び1-メチル-4-(1-((2-フェニルシクロヘキシル)オキシ)プロペ-1-エン-2-イル)ベンゼンを除く、化合物。(2-((3-methylbut-2-en-1-yl)oxy)vinyl)benzene, (1-(isopentyloxy)prop-1-en-2-yl)benzene, (2-(pentyloxy) (vinyl)benzene, (1-(dodecyloxy)prop-1-en-2-yl)benzene, (2-(hexyloxy)vinyl)benzene, (2-(heptyloxy)vinyl)benzene, (2-(octyl) oxy)vinyl)benzene, (1-(2-cyclohexylethoxy)prop-1-en-2-yl)benzene, 2-(3,7-dimethyloct-2,6-dien-1-yl)oxy)vinyl ) Benzene, (2-phenetoxyvinyl)benzene, (2-(cyclohexyloxy)vinyl)benzene, 1-(2-(cyclohexyloxy)vinyl)-4-methoxybenzene, (1-(2-cyclohexylethoxy)prope -1-en-2-yl)benzene and 1-methyl-4-(1-((2-phenylcyclohexyl)oxy)prop-1-en-2-yl)benzene.
i) 請求項11において定義した式(I)の化合物の少なくとも1つ、
ii) 香料キャリヤー及び香料ベースからなる群から選択される成分の少なくとも1つ、並びに
iii) 任意に香料補助剤の少なくとも1つ
を含む、付香組成物。 below,
i) at least one compound of formula (I) as defined in claim 11 ;
A perfuming composition comprising ii) at least one ingredient selected from the group consisting of a perfume carrier and a perfume base, and iii ) optionally at least one perfume adjuvant.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862689017P | 2018-06-22 | 2018-06-22 | |
US62/689,017 | 2018-06-22 | ||
EP18188738.1 | 2018-08-13 | ||
EP18188738 | 2018-08-13 | ||
PCT/EP2019/066356 WO2019243501A1 (en) | 2018-06-22 | 2019-06-20 | Enol ether properfume |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2021527720A JP2021527720A (en) | 2021-10-14 |
JPWO2019243501A5 true JPWO2019243501A5 (en) | 2023-10-12 |
JP7416708B2 JP7416708B2 (en) | 2024-01-17 |
Family
ID=66867168
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2020550628A Active JP7416708B2 (en) | 2018-06-22 | 2019-06-20 | enol ether pro fragrance |
Country Status (8)
Country | Link |
---|---|
US (2) | US11667869B2 (en) |
EP (1) | EP3746420B1 (en) |
JP (1) | JP7416708B2 (en) |
CN (1) | CN111936457A (en) |
BR (1) | BR112020018516B1 (en) |
ES (1) | ES2960448T3 (en) |
MX (1) | MX2020009659A (en) |
WO (1) | WO2019243501A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR112021018601A2 (en) | 2019-03-20 | 2021-11-23 | Firmenich & Cie | Encapsulated pro-perfume compounds |
US20220259524A1 (en) | 2019-06-27 | 2022-08-18 | Firmenich Sa | Perfumed consumer products |
US20230024269A1 (en) * | 2019-12-20 | 2023-01-26 | Firmenich Sa | Pro-Perfume Compositions |
MX2022015145A (en) | 2020-06-12 | 2023-01-11 | Firmenich & Cie | Enol ether properfume. |
WO2023111006A1 (en) | 2021-12-14 | 2023-06-22 | Firmenich Sa | Enol ether properfume |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59167531A (en) * | 1983-03-12 | 1984-09-21 | Toyotama Koryo Kk | Production of beta-phenylethylisoamyl ether |
EP0888439A1 (en) * | 1996-03-22 | 1999-01-07 | The Procter & Gamble Company | Detergent compositions containing fragrance precursors and the fragrance precursors themselves |
ES2183313T3 (en) * | 1997-06-23 | 2003-03-16 | Givaudan Sa | CARBONATES FOR THE GENERATION OF ALDEHIDS AND / OR KETONES. |
DE10032335A1 (en) * | 2000-07-04 | 2002-01-17 | Cognis Deutschland Gmbh | Dimethylbenzene derivatives |
US8557262B2 (en) * | 2008-09-12 | 2013-10-15 | Firmenich Sa | Divinyl ether derivatives capable of releasing active aldehydes and ketones and methods of use for perfuming surfaces |
US8168834B2 (en) * | 2009-11-16 | 2012-05-01 | International Flavors & Fragrances Inc. | 4-alkyl 1-(3-methoxy-2-propen-1-yl) benzene compounds and their use in perfume compositions |
GB201021864D0 (en) * | 2010-12-23 | 2011-02-02 | Givaudan Sa | Organic compounds |
CN105143163B (en) * | 2013-05-08 | 2019-10-29 | 弗门尼舍有限公司 | Preceding aroma compounds |
-
2019
- 2019-06-20 BR BR112020018516-7A patent/BR112020018516B1/en active IP Right Grant
- 2019-06-20 CN CN201980023317.8A patent/CN111936457A/en active Pending
- 2019-06-20 MX MX2020009659A patent/MX2020009659A/en unknown
- 2019-06-20 JP JP2020550628A patent/JP7416708B2/en active Active
- 2019-06-20 ES ES19730850T patent/ES2960448T3/en active Active
- 2019-06-20 US US16/981,152 patent/US11667869B2/en active Active
- 2019-06-20 EP EP19730850.5A patent/EP3746420B1/en active Active
- 2019-06-20 WO PCT/EP2019/066356 patent/WO2019243501A1/en unknown
-
2023
- 2023-04-24 US US18/138,349 patent/US20230257678A1/en active Pending
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