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832-09-7

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832-09-7 Usage

General Description

CIS-1,3-DIACETOXYCYCLOHEXANE is a chemical compound with the molecular formula C10H16O4. It is a cyclic organic compound that contains a cyclohexane ring with two acetoxy groups attached in the cis configuration. CIS-1,3-DIACETOXYCYCLOHEXANE is often used as a reagent in organic synthesis, particularly in the formation of complex organic molecules. It is important in the pharmaceutical and biotechnology industries for the development of new drugs and biologically active compounds. Additionally, CIS-1,3-DIACETOXYCYCLOHEXANE has applications in the production of perfumes and fragrances, as well as in the formulation of certain types of coatings and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 832-09-7 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 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 832-09:
(5*8)+(4*3)+(3*2)+(2*0)+(1*9)=67
67 % 10 = 7
So 832-09-7 is a valid CAS Registry Number.

832-09-7SDS

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 [(1S,3R)-3-acetyloxycyclohexyl] acetate

1.2 Other means of identification

Product number -
Other names cis-Cyclohexan-1,3-dioldiacetat

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:832-09-7 SDS

832-09-7Downstream Products

832-09-7Relevant articles and documents

Enzymatic resolution, desymmetrization, and dynamic kinetic asymmetric transformation of 1,3-cycloalkanediols

Fransson, Ann-Britt L.,Xu, Yongmei,Leijondahl, Karin,Baeckvall, Jan-E.

, p. 6309 - 6316 (2007/10/03)

An efficient desymmetrization of cis-1,3-cyclohexanediol to (1S,3R)-3-(acetoxy)-1-cyclohexanol ((R,S)-2a) was performed via Candida antarctica lipase B (CALB)-catalyzed transesterification, in high yield (up to 93%) and excellent enantioselectivity (ee's

Rhodium(I)-Catalyzed Hydroboration of Olefins. The Documentation of Regio- and Stereochemical Control in Cyclic and Acyclic Systems

Evans, David A.,Fu, Gregory C.,Hoveyda, Amir H.

, p. 6917 - 6918 (2007/10/02)

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