52610-46-5

Basic information

• Product Name: 2-Cyclohexene-1-methanol,2,6,6-trimethyl-R- 1-propenyl-
• CAS NO: 52610-46-5
• Molecular Weight: 194.317
• Mol File: 52610-46-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexene-1-methanol,2,6,6-trimethyl-R- 1-propenyl- (CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexene-1-methanol,2,6,6-trimethyl-R- 1-propenyl- (52610-46-5)
• EPA Substance Registry System: 2-Cyclohexene-1-methanol,2,6,6-trimethyl-R- 1-propenyl- (52610-46-5)

Safety Data

• Hazardous Substances Data: 52610-46-5(Hazardous Substances Data)

Upstream product

• 124572-59-4 α-ionone epoxyhydrazone 
• 17522-32-6 (S)-dehydro-α-damascol 
• 139609-03-3 2-(1-Bromoethyl)-3-(2,6,6-trimethyl-2-cyclohexen-1-yl)oxirane 
• 127-41-3 alpha-ionone 
• 37079-64-4 1-<3-(2,6,6-Trimethyl-2-cyclohexen-1-yl)oxiranyl>ethanone 
• 139609-01-1 α-Methyl-3-(2,6,6-trimethyl-2-cyclohexen-1-yl)oxiranemethanol 
• 134780-16-8 (R)-2,4,4-trimethyl-2-cyclohexen-1-ol 
• 14505-74-9 (S)-2,6,6-trimethylcyclohex-2-enecarbaldehyde 
• 52646-93-2 [(S)-2,6,6-trimethylcyclohex-2-enyl]methanol 
• 13395-71-6 2,4,4-trimethyl-2-cyclohexenone 
• 37079-64-4 1-[3-(2,6,6-trimethyl-cyclohex-2-enyl)-oxiranyl]-ethanone 

Downstream Products

• 127-41-3 alpha-ionone 
• 57549-92-5 ⁽²⁾-1-(2,6,6-trimethylcyclohex-2-en-1-yl)butan-1-one 
• 116497-11-1 (2E)-1-[(S)-2,6,6-trimethylcyclohex-2-enyl]but-2-en-1-one 
• 23726-94-5 (Z)-1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-2-buten-1-one 
• 24720-09-0 α-damascone 

Relevant articles and documents

Synthesis of (S-α-damascone

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APPLICATION OF BIOCHEMICAL METHODS IN ENANTIOSELECTIVE SYNTHESIS OF BIOACTIVE NATURAL PRODUCTS

Enzymes as well as yeasts were used in enantioselective syntheses of bioregulators such as hormones and semiochemicals.Lipases and esterases were employed in achieving optical resolution, conversion of meso-compounds to optically active compounds, and macrolactonization.Lactase effected glucosidation of a phenolic hydroxy ketone without any protection of the functional groups.Yeasts provided a variety of optically active hydroxy esters and ketones, which served as versatile non-racemic chiral building blocks.

Alkenoyl-cyclohexadienes

New cycloaliphatic unsaturated ketones and their use as perfuming and odour-modifying agents in the manufacture of perfumes and perfumed products, and as flavouring and taste-modifying agents in the preparation of foodstuffs in general and imitation flavours for foodstuffs, beverages, animal feeds, pharmaceutical preparations and tobacco products. Methods for the preparation of said cycloaliphatic unsaturated ketones.