albicanol

[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl]methanol

CAS: 54632-04-1 C15 H26 O MW: 222.37142000

Identification

Namealbicanol
IUPAC[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methanol
CAS Number54632-04-1
FDA UNIISearch
Molecular FormulaC15 H26 O
Molecular Weight222.37142000
Nikkaji NumberJ13.110E

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 ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for albicanol usage levels up tonot for fragrance use.
Recommendation for albicanol flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

found in nature

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.