145631-62-5

Basic information

• Product Name: 7-hydroxy-6,11-cyclofarnes-3(15)-en-2-one
• Synonyms: 7-hydroxy-6,11-cyclofarnes-3(15)-en-2-one
• CAS NO: 145631-62-5
• Molecular Formula: C15H26O2
• Molecular Weight: 238.36574
• Mol File: 145631-62-5.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7-hydroxy-6,11-cyclofarnes-3(15)-en-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-hydroxy-6,11-cyclofarnes-3(15)-en-2-one(145631-62-5)
• EPA Substance Registry System: 7-hydroxy-6,11-cyclofarnes-3(15)-en-2-one(145631-62-5)

Safety Data

• Hazardous Substances Data: 145631-62-5(Hazardous Substances Data)

Upstream product

• 178616-52-9 Toluene-4-sulfonic acid 2-[2-(2-hydroxy-2,6,6-trimethyl-cyclohexyl)-ethyl]-3-oxo-butyl ester 
• 41641-14-9 1-hydroxymethyl-3,3-dimethyl-cyclohex-1-ene 
• 84078-59-1 2-(2'-Methylene-6',6'-dimethylcyclohexyl)ethanol 
• 67218-06-8 6-(butylsulfanyl-methylene)-2,2-dimethyl-cyclohexanone 
• 76337-18-3 3,3-Dimethylcyclohex-1-ene-1-carbaldehyde 
• 88214-43-1 1-<2'-(p-Toluenesulfonyl)ethyl>-2-methylene-6,6-dimethylcyclohexane 
• 99440-31-0 Ethyl 2-(6,6-dimethyl-2-methylenecyclohexyl)ethanoate 
• 178616-59-6 (+/-)-2-(2-Iodoethyl)-3-methylene-1,1-dimethylcyclohexane 
• 178616-56-3 6-[1-Butylsulfanyl-meth-(Z)-ylidene]-2,2-dimethyl-cyclohexanol 
• 178616-60-9 (2R*S*,1'R*)-Methyl 2-<2-(6-methylene-2,2-dimethylcyclohexyl)ethyl>-3-oxobutanoate 
• 178616-61-0 Methyl 2-<2-(6-epoxymethylene-2,2-dimethylcyclohexyl)ethyl>-3-oxobutanoate 
• 178616-50-7 2-[2-(2-Hydroxy-2,6,6-trimethyl-cyclohexyl)-ethyl]-butane-1,3-diol 
• 178616-51-8 3-Hydroxymethyl-5-(2-hydroxy-2,6,6-trimethyl-cyclohexyl)-pentan-2-one 
• 472-63-9 2-(2,6,6-trimethyl-cyclohex-2-enyl)-ethanol 

Relevant articles and documents

An Efficient Alternative Synthesis of (+)-(6S,7S)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the (S)-Enantiomer of the Antibacterial Sesquiterpene from Premna oligotricha

The title compound has been synthesized from optically active lactone derived from (S)-(+)-Wieland-Miescher ketone analogue employing solid-state Baeyer-Villiger reaction.

Synthesis of mono- and sesquiterpenoids, XXV: Synthesis of (6R*,7R*)-7-hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the racemate of the antibacterial sesquiterpene from premna oligotricha, and its (6R*,7R*) isomer

The structure of the antibacterial sesquiterpene from Premna oligotricha was shown to be not 1 but 2 (relative stereochemistry) by the unambiguous synthesis of both (±)-1 and (±)-2. VCH Verlagsgesellschaft mbH, 1996.