15356-74-8
15356-74-8
Chemical Structure
(±)-Dihydroactinidiolide
- CAS No.: 15356-74-8
- Formula:C11H16O2
- Molecular Weight:180.25
IUPAC Name: 4,4,7a-trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one
InChIKey: IMKHDCBNRDRUEB-UHFFFAOYSA-N
SMILES: O=C1OC2(C)C(C(C)(C)CCC2)=C1
Biological Activity: (±)-Dihydroactinidiolide is the dextrorotatory form of Dihydroactinidiolide (HY-107805). (±)-Dihydroactinidiolide has a strong, pleasant musky, tea-like and tobacco-like aroma and is mainly found in black tea, tobacco and fruits. (±)-Dihydroactinidiolide has antioxidant activity and can be derived from β-carotene.or light adaptation in Arabidopsis[1][2][3].
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(±)-Dihydroactinidiolide | 99.80% | (±)-Dihydroactinidiolide is the dextrorotatory form of Dihydroactinidiolide (HY-107805). (±)-Dihydroactinidiolide has a strong, pleasant musky, tea-like and tobacco-like aroma and is mainly found in black tea, tobacco and fruits. (±)-Dihydroactinidiolide has antioxidant activity and can be derived from β-carotene.or light adaptation in Arabidopsis. | ||||||||||||||||||||
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(±)-Dihydroactinidiolide (Standard) | ≥98% | (±)-Dihydroactinidiolide (Standard) is the analytical standard of (±)-Dihydroactinidiolide (HY-W041301). This product is intended for research and analytical applications. (±)-Dihydroactinidiolide is the dextrorotatory form of Dihydroactinidiolide (HY-107805). (±)-Dihydroactinidiolide has a strong, pleasant musky, tea-like and tobacco-like aroma and is mainly found in black tea, tobacco and fruits. (±)-Dihydroactinidiolide has antioxidant activity and can be derived from β-carotene. | ||||||||||||||||||||
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References
- [1]. Kaneko H, et, al. The Aroma of Cigar Tobacco. Part I. Isolation of 2-Hydroxy-2,6,6-trimethylcyclohexylidene-1-acetic Acid Lactone (Dihydroactinidiolide) from Ether Extract of Cigar Leaves. Agricultural and Biological Chemistry. 1968 Jou; 32(11): 1337-40.
- [2]. Bosser A, et, al. A Simple Way to (±)-Dihydroactinidiolide from β-Ionone Related to the Enzymic Co-oxidation of β-Carotene in Aqueous Solution. Biotechnology Progress. 1995 Jou; 11(6): 689-92.
- [3]. Ferdosh S, et al. Extraction of Bioactive Compounds and Evaluation of Antioxidant Activity from Senna alata Linn Leaves using Subcritical Carbon Dioxide Soxhlet and Conventional Methods. The Natural Products Journal. 2025 Nov;15(8):E250724232281.
