55511-67-6

Basic information

• Product Name: 1-(4-methyl-3-cyclohexen-1-yl)ethanol
• Synonyms: 1-(4-methyl-3-cyclohexen-1-yl)ethanol
• CAS NO: 55511-67-6
• Molecular Weight: 140.225
• Mol File: 55511-67-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-(4-methyl-3-cyclohexen-1-yl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methyl-3-cyclohexen-1-yl)ethanol(55511-67-6)
• EPA Substance Registry System: 1-(4-methyl-3-cyclohexen-1-yl)ethanol(55511-67-6)

Safety Data

• Hazardous Substances Data: 55511-67-6(Hazardous Substances Data)

Upstream product

• 29548-14-9 α-4-dimethyl-3-cyclohexene-1-acetaldehyde 
• 18479-68-0 menth-1-en-9-ol 
• 138-86-3 limonene. 
• 7560-64-7 4-methyl-cyclohex-3-enecarbaldehyde 
• 75-16-1 methylmagnesium bromide 
• 64-17-5 ethanol 
• 6090-09-1 (+-)-4-acetyl-1-methylcyclohexene 
• 60-29-7 diethyl ether 
• 203719-53-3 (-)-limonene oxide 
• 6090-09-1 methyl-[(1S)-4-methylcyclohex-3-enyl]ketone 

Downstream Products

• 622-96-8 4-methylethylbenzene 
• 34884-20-3 1-(4-methylcyclohexyl)-1-ethanol 
• 6090-09-1 (+-)-4-acetyl-1-methylcyclohexene 
• 73416-67-8 (E)-ethyl 3-(4-methylcyclohex-3-en-1-yl)-2-butenoate 
• 108448-75-5 3-(4-methyl-3-cyclohexen-1-yl)-but-2(E)-enoic acid 
• 69401-36-1 vestitenone 
• 17916-91-5 Acetic acid 1-(4-methyl-cyclohex-3-enyl)-ethyl ester 
• 18446-94-1 1-((trans)-4-methylcyclohexyl)ethanol 
• 18446-93-0 cis-1-(1-Hydroxy-ethyl)-4-methyl-cyclohexan 
• 7322-63-6 cis-p-menthan-8-ol 

Relevant articles and documents

SELECTIVE REDUCTION OF CARBONYL COMPOUNDS BY DIPHENYLSTIBINE

Carbonyl compounds were selectively reduced by diphenylstibine in the presence of Lewis acid.

Odor-active constituents of Cedrus atlantica wood essential oil

The main odorant constituents of Cedrus atlantica essential oil were characterized by GC-Olfactometry (GC-O), using the Aroma Extract Dilution Analysis (AEDA) methodology with 12 panelists. The two most potent odor-active constituents were vestitenone and 4-acetyl-1-methylcyclohexene. The identification of the odorants was realized by a detailed fractionation of the essential oil by liquid-liquid basic extraction, distillation and column chromatography, followed by the GC-MS and GC-O analyses of some fractions, and the synthesis of some non-commercial reference constituents.

Biosynthesis of verrucarin and roridin derivatives. V. Synthesis of two pairs of diastereoisomers of (1,8 C14) α bisabolol and attempts to incorporate these in verrucarol

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