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113391-96-1

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113391-96-1 Usage

Type of Compound

Organic compound

Derivative

Cyclohexanediol

Usage

Reagent in organic chemistry reactions

Isomer

Trans isomer

Hydroxyl Group Position

Opposite sides of the cyclohexane ring

Applications

a. Synthesis of various organic compounds
b. Production of pharmaceuticals
c. Manufacturing of polymers
d. Production of other industrial chemicals

Importance

Building block for the synthesis of various organic compounds

Industries

Wide range of industries, including pharmaceutical, polymer, and chemical manufacturing

Check Digit Verification of cas no

The CAS Registry Mumber 113391-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,9 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113391-96:
(8*1)+(7*1)+(6*3)+(5*3)+(4*9)+(3*1)+(2*9)+(1*6)=111
111 % 10 = 1
So 113391-96-1 is a valid CAS Registry Number.

113391-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (+-)-cis-1-methanesulfonyloxy-cyclohexanol-(2)

1.2 Other means of identification

Product number -
Other names (+-)-cis-1-Methansulfonyloxy-cyclohexanol-(2)

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:113391-96-1 SDS

113391-96-1Relevant articles and documents

A novel application of the base induced mesyl elimination

Pestchanker,Giordano

, p. 463 - 464 (1990)

The preparation of ketones from cis glycols in a two steps process initiated by a mesylation step followed by a base induced elimination is reported.

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