20993-80-0

Basic information

• Product Name: (1R,1'S,2'S)-1-(2'-Methyl-cyclohexyl)-ethanol
• CAS NO: 20993-80-0
• Molecular Weight: 142.241
• Mol File: 20993-80-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1R,1'S,2'S)-1-(2'-Methyl-cyclohexyl)-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,1'S,2'S)-1-(2'-Methyl-cyclohexyl)-ethanol(20993-80-0)
• EPA Substance Registry System: (1R,1'S,2'S)-1-(2'-Methyl-cyclohexyl)-ethanol(20993-80-0)

Safety Data

• Hazardous Substances Data: 20993-80-0(Hazardous Substances Data)

Upstream product

• 2047-97-4 2-methyl-1-acetyl-1-cyclohexene 
• 60-29-7 diethyl ether 
• 30502-73-9 2,8-nonanedione 
• 577-16-2 2-Methylacetophenone 
• 13955-60-7 1-(2-methyl-cyclohex-3-enyl)-ethanone 
• 55169-94-3 1-(5-methylcyclohex-3-enyl)ethanone 

Downstream Products

• 4923-77-7 1-methyl-2-ethylcyclohexane 
• 64811-81-0 1-(2-methylcyclohexyl)ethanone 
• 1533-89-7 trans-1-methyl-2-vinylcyclohexane 
• 1533-89-7 cis-1-methyl-2-vinylcyclohexane 

Relevant articles and documents

Chemoselective hydrogenation of aromatic ketones with Pt-based heterogeneous catalysts. Substituent effects

Catalytic reduction of aromatic ketones is an interesting reaction that leads to the obtaining of alcohols. Some of these alcohols are employed as intermediaries to produce chemical fine compounds. The bimetallic catalysts are widely used in the chemoselective hydrogenation. The Surface Organometallic Chemistry on Metals (SOMC/M) is a methodology employed to obtain bimetallic systems. In the present work the hydrogenation of ketones derived from acetophenone has been studied. The aim was observe the effect on activity and selectivity to aromatic alcohols by the presence of substituents in the ring. The chemical characteristics of substituents groups could influence the way aromatic ketones are absorbed on the metallic surface. This fact can be explained by a combination of geometric and electronic effects.

ALICYCLIC ESTER WITH MUSK FRAGRANCE

A compound of formula (I) or (II) is disclosed, whereby, in formulas (I) and (II), R1 = an optionally-substituted (a) branched or unbranched C1 to C5 alkyl, or (b) branched or unbranched C2 to C5 alkylene, or (c) C3 to C5 cycloalkyl and in formula (II) the bond represented by a dotted line may be either a single- or a double-bond.