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56137-57-6

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56137-57-6 Usage

Type of compound

Cyclic diol

Structure

Contains two hydroxyl groups attached to a cyclohexane ring

Presence of methyl groups

Two methyl groups are present at the 1st and 4th carbon positions of the cyclohexane ring

Industrial applications

a. Solvent
b. Starting material in the synthesis of other organic compounds
c. Production of polymers and resins

Additional uses

a. Corrosion inhibitor
b. Component in hydraulic fluids

Importance

Versatile and significant compound in organic chemistry and industrial manufacturing

Check Digit Verification of cas no

The CAS Registry Mumber 56137-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,3 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56137-57:
(7*5)+(6*6)+(5*1)+(4*3)+(3*7)+(2*5)+(1*7)=126
126 % 10 = 6
So 56137-57-6 is a valid CAS Registry Number.

56137-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dimethylcyclohexane-1,4-diol

1.2 Other means of identification

Product number -
Other names 1,4-Dimethyl-3-cyclohexen-1-carbonsaeure

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:56137-57-6 SDS

56137-57-6Downstream Products

56137-57-6Relevant articles and documents

Selective C-H bond hydroxylation of cyclohexanes in water by supramolecular control

Yang, Bin,Cui, Jian-Fang,Wong, Man Kin

, p. 30886 - 30893 (2017/07/07)

A new approach for selective hydroxylation of non-activated cyclohexanes using dioxirane generated in situ in water through supramolecular control has been developed. Using β-CD and γ-CD as the supramolecular hosts, selective hydroxylation of cyclohexane substrates, including trans/cis-1,4-, 1,3-and 1,2-dimethylcyclohexanes and trans/cis-decahydronaphthalene, was achieved in up to 54% yield in water. Furthermore, site-selective C-H bond hydroxylation of (+)-menthol was achieved by obstructing the approach of dioxirane to the C-H bond with higher steric hindrance through inclusion complexation with β-CD and γ-CD in water.

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