831-13-0

Usage

Chemical structure

A cyclohexene ring attached to a phenyl group, with a methanol molecule also attached.

Common uses

As a fragrance ingredient in perfumes and other cosmetic products.

Aroma

Floral, sweet, and woody.

Industry popularity

Popular in the fragrance industry.

Additional uses

Used in the production of flavors and fragrances for food and beverages.

Potential applications

Has potential applications in pharmaceuticals and agrochemicals.

Versatility

A versatile compound with a range of uses in various industries.

InChI:InChI=1/C13H16O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-5,7-8,12-14H,6,9-10H2

Upstream product

• 100-50-5 3-Cyclohexene-1-carboxaldehyde 
• 100-52-7 benzaldehyde 
• 1165952-91-9 cyclohexa-1,3-diene 
• 100-58-3 phenylmagnesium bromide 

Downstream Products

• 712-50-5 Cyclohexyl phenyl ketone 
• 831-14-1 cyclohex-3-en-1-yl(phenyl)methanone 
• 834-42-4 1--1-phenyl-prop-2-in-1-ol 

Relevant academic research and scientific papers

Rhodium-Catalyzed Remote Isomerization of Alkenyl Alcohols to Ketones

We develop herein an efficient rhodium-catalyzed remote isomerization of aromatic and aliphatic alkenyl alcohols into ketones. This catalytic process, with a commercially available catalyst and ligand ([RhCl(cod)]2 and Xantphos), features high efficiency, low catalyst loading, good functional group tolerance, a broad substrate scope, and no (sub)stoichiometric additive. Preliminary mechanistic studies suggest that this transformation involves an iterative dissociative β-hydride elimination-migration insertion process.

Nickel-catalyzed homoallylation reaction of aldehydes with 1,3-dienes: Stereochemical and mechanistic studies

(Matrix presented) Contrary to what was reported, the coupling reaction of nickel-catalyzed cyclic diene such as cyclohexadiene with carbonyl compounds in the presence of diethyl zinc afforded γ,δ-alkenyl alcohols in good yields.