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Phenol, 4-(1-chloroethyl)-2,6-bis(1,1-dimethylethyl)-, also known as 2,6-di-tert-butyl-4-chloromethylphenol, is a chemical compound with the molecular formula C14H22ClO. It is a white crystalline solid that is soluble in most organic solvents. Phenol, 4-(1-chloroethyl)-2,6-bis(1,1-dimethylethyl)- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as an antioxidant and a stabilizer in the production of polymers. Due to its reactivity, it is essential to handle Phenol, 4-(1-chloroethyl)-2,6-bis(1,1-dimethylethyl)- with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

7050-91-1

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7050-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7050-91-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,5 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7050-91:
(6*7)+(5*0)+(4*5)+(3*0)+(2*9)+(1*1)=81
81 % 10 = 1
So 7050-91-1 is a valid CAS Registry Number.

7050-91-1SDS

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 2,6-ditert-butyl-4-(1-chloroethyl)phenol

1.2 Other means of identification

Product number -
Other names 2,6-di-t-butyl-4-chloroethylphenol

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:7050-91-1 SDS

7050-91-1Upstream product

7050-91-1Relevant academic research and scientific papers

Process for the preparation of 3,5-dihydrocarbyl-4-hydroxybenzylmalonic acid esters

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, (2008/06/13)

Esters of 3,5-dihydrocarbyl-4-hydroxybenzylmalonic acid are prepared by reacting a 2,6-dihydrocarbyl-4-halomethylphenol with an ester of a 1,3-dicarboxylic acid in the presence of an alkali or an alkaline earth metal hydride. The products are useful as antioxidants.

Antioxidant ester substituted phenols and process for their preparation

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, (2008/06/13)

This invention comprises an alkylation, reduction and transesterification process for the preparation of ester substituted phenols. The products are useful as antioxidants and may be prepared in high yields and with a high degree of purity.

Preparation of antioxidants

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, (2008/06/13)

This invention comprises an alkylation, reduction and transesterification process for the preparation of ester substituted phenols. The products are useful as antioxidants and may be prepared in high yields and with a high degree of purity.

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