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4773-40-4

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4773-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4773-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,7 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4773-40:
(6*4)+(5*7)+(4*7)+(3*3)+(2*4)+(1*0)=104
104 % 10 = 4
So 4773-40-4 is a valid CAS Registry Number.

4773-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butyl-6-[1-(3-tert-butyl-2-hydroxy-5-methylphenyl)ethyl]-4-methylphenol

1.2 Other means of identification

Product number -
Other names 6,6'-Di-tert-butyl-4,4'-dimethyl-2,2'-aethyliden-di-phenol

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:4773-40-4 SDS

4773-40-4Downstream Products

4773-40-4Relevant articles and documents

Production of bisphenol monoester

-

, (2008/06/13)

A bisphenol monoester represented by the formula (I): STR1 wherein R1 is hydrogen or alkyl, R2 and R3 are each alkyl, and R4 is alkyl, alkenyl or phenyl, is produced by continuous two step reactions in which an aldehyde R1 -CHO and 2,4-dialkylphenol are subjected to a condensation reaction in a C6 -C10 aliphatic or C6 -C12 aromatic hydrocarbon solvent, and then a resulting bisphenol compound dissolved in the solvent is subjected to an esterification with a carboxylic acid R4 --COOH or its derivative. Prior to the esterification, the organic layer containing the bisphenol compound is subjected to a dehydration treatment, thereby enabling the two steps to proceed continuously without isolating the intermediate bisphenol compound. A purification process for the bisphenol monoester of the formula (I) is also disclosed in which the monoester is purified from a mixed solvent comprising a C6 -C12 aromatic hydrocarbon solvent and a C1 -C8 alcohol or C2 -C3 aliphatic nitrile solvent.

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