albicanol
[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl]methanol
Identification
| Name | albicanol |
| IUPAC | [(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methanol |
| CAS Number | 54632-04-1 |
| FDA UNII | Search |
| Molecular Formula | C15 H26 O |
| Molecular Weight | 222.37142000 |
| Nikkaji Number | J13.110E |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 299.34 °C. @ 760.00 mm Hg (est) |
| Flash Point | 225.00 °F. TCC ( 107.30 °C. ) (est) |
| logP (o/w) | 4.661 (est) |
| Soluble in | water, 7.289 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for albicanol usage levels up to | not for fragrance use. |
| Recommendation for albicanol flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
1-
naphthalenemethanol, decahydro-5,5,8a-trimethyl-2-methylene-, (1S,4aS,8aS)-
[(1S,4aS,8aS)-5,5,8a-
trimethyl-2-methylenedecahydronaphthalen-1-yl]methanol
[(1S,4aS,8aS)-5,5,8a-
trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methanol
PubMed:
Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus.
PubMed:
Further drimane sesquiterpenes from Drimys brasiliensis stem barks with cytotoxic potential.
PubMed:
Compounds from Dryopteris fragrans (L.) Schott with cytotoxic activity.
PubMed:
Cytotoxic metabolites from Perenniporia tephropora, an endophytic fungus from Taxus chinensis var. mairei.
PubMed:
First syntheses of (-)-tauranin and antibiotic (-)-BE-40644 based on lipase-catalyzed optical resolution of albicanol.
PubMed:
A concise Diels-Alder strategy for the asymmetric synthesis of (+)-albicanol, (+)-albicanyl acetate, (+)-dihydrodrimenin, and (-)-dihydroisodrimeninol.
PubMed:
Concise syntheses of coronarin A, coronarin E, austrochaparol and pacovatinin A.
PubMed:
[Study on terpene of Dryopteris fragrans L].
PubMed:
Total syntheses of (+)-chloropuupehenone and (+)-chloropuupehenol and their analogues and evaluation of their bioactivities.
PubMed:
African elephant sesquiterpenes. II. Identification and synthesis of new derivatives of 2,3-dihydrofarnesol.
PubMed:
Cryptoporic and isocryptoporic acids from the fungal cultures of Polyporus arcularius and P. ciliatus.
PubMed:
First synthesis of (+)-alpha- and (+)-gamma-polypodatetraenes.
PubMed:
Total synthesis of (+)-albicanol and (+)-albicanyl acetate.
PubMed:
Ichthyotoxic phloroglucinol derivatives from Dryopteris fragrans and their anti-tumor promoting activity.