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4,4-bis(4-hydroxyphenyl)cyclohexanecarboxylic acid ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116779-06-7

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116779-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116779-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,7 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116779-06:
(8*1)+(7*1)+(6*6)+(5*7)+(4*7)+(3*9)+(2*0)+(1*6)=147
147 % 10 = 7
So 116779-06-7 is a valid CAS Registry Number.

116779-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4-bis(4-hydroxyphenyl)cyclohexanecarboxylic acid ester

1.2 Other means of identification

Product number -
Other names 4,4-bis(4-hydroxyphenyl)cyclohexanecarboxylic acid

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:116779-06-7 SDS

116779-06-7Relevant academic research and scientific papers

4,4-bis(4-hydroxyphenyl)cyclohexanecarboxylic acid derivatives and process for preparing same

-

, (2008/06/13)

Novel 4,4-bis(4-hydroxyphenyl)cyclohexanecarboxylic acid derivatives. These compounds can be prepared by reacting a cyclohexanone-4-carboxylic acid with a phenol.

Process for the preparation of 4'-hydroxybiphenyl-4-carboxyl acid

-

, (2008/06/13)

A process for the preparation of 4'-hydroxybiphenyl-4-carboxylic acid by reacting a cyclohexanone-4-carboxylic acid compound with phenol in the presence of an acid catalyst, and then subjecting the resulting 4,4-bis(4-hydroxyphenyl)cyclohexanecarboxylic acid compound to decomposition and dehydrogenation reactions in the presence of a base and a dehydrogenation catalyst. The aforesaid cyclohexanone-4-carboxylic acid compound is obtained by catalytically hydrogenating a 4-hydroxybenzoic acid compound in a secondary alcohol or tertiary alcohol solvent, and the reaction mixture thus obtained is directly used for the reaction with phenol.

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