Name | Dihydroactinidiolide |
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Synonyms |
dihydroactinidiolide
T56 BVO AH&TJ A1 F1 F1 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (S)- 2-Hydroxy-2,6,6-trimethylcyclohexylideneacetic acid γ-lactone 5,6,7,7a-Tetrahydro-4,4,7a-trimethyl-2(4H)-benzofuranone 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl-, (7aS)- (±)-(2,6,6,-Trimethyl-2-hydroxycyclohexylidene)acetic acid γ-lactone 4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one 4,4,7a-Trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one UNII:BH8469LVA9 (7aS)-4,4,7a-Trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl- |
Description | (±)-Dihydroactinidiolide, an important aroma compound of black tea and tobacco, has been isolated from several plants. (±)-Dihydroactinidiolide can be formation from β-Carotene by the treatment of polyphenoloxidase, the lipoxygenase, and the xanthine oxidase[1][2]. |
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Related Catalog | |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 296.1±9.0 °C at 760 mmHg |
Melting Point | 42-43° |
Molecular Formula | C11H16O2 |
Molecular Weight | 180.243 |
Flash Point | 120.2±16.1 °C |
Exact Mass | 180.115036 |
PSA | 26.30000 |
LogP | 2.26 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.504 |
Storage condition | 2-8°C |
Hazard Codes | Xi |
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Precursor 8 | |
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DownStream 0 |