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56137-58-7

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56137-58-7 Usage

Type of compound

Diol (contains two hydroxyl groups)

Derived from

Cyclohexane

Industrial applications

Production of adhesives
Production of sealants
Production of coatings
Production of resins

Additional uses

As a solvent
As a plasticizer

Volatility

Low

Toxicity

Low (considered relatively safe for industrial applications)

Check Digit Verification of cas no

The CAS Registry Mumber 56137-58-7 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 56137-58:
(7*5)+(6*6)+(5*1)+(4*3)+(3*7)+(2*5)+(1*8)=127
127 % 10 = 7
So 56137-58-7 is a valid CAS Registry Number.

56137-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 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 1r,4c-Dimethyl-cyclohexan-1,4t-diol

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:56137-58-7 SDS

56137-58-7Downstream Products

56137-58-7Relevant 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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