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831-13-0

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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.

Check Digit Verification of cas no

The CAS Registry Mumber 831-13-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 831-13:
(5*8)+(4*3)+(3*1)+(2*1)+(1*3)=60
60 % 10 = 0
So 831-13-0 is a valid CAS Registry Number.
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

831-13-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohex-3-en-1-yl(phenyl)methanol

1.2 Other means of identification

Product number -
Other names Cyclohexen-3-ylphenylcarbinol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:831-13-0 SDS

831-13-0Relevant articles and documents

Rhodium-Catalyzed Remote Isomerization of Alkenyl Alcohols to Ketones

Dong, Wenke,Yang, Hongxuan,Yang, Wen,Zhao, Wanxiang

supporting information, (2020/02/28)

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.

THE EFFECT OF ALKYL SUBSTITUTION IN DRUGS. XI. THE SYNTHESIS OF SOME

VAN DER STELT,FUNCKE,NAUTA

, p. 1161 - 1162 (2007/10/14)

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