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Benzoyl chloride, 2-(2-chloro-2-oxoethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129228-76-8

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129228-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129228-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,2,2 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129228-76:
(8*1)+(7*2)+(6*9)+(5*2)+(4*2)+(3*8)+(2*7)+(1*6)=138
138 % 10 = 8
So 129228-76-8 is a valid CAS Registry Number.

129228-76-8SDS

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-(2-chloro-2-oxoethoxy)benzoyl chloride

1.2 Other means of identification

Product number -
Other names 2-Chlorcarbonylmethoxy-benzoylchlorid

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:129228-76-8 SDS

129228-76-8Relevant academic research and scientific papers

Use of Phosphorus Pentoxide. Preparation of Half-esters through Selective Esterification

Banerjee, Amalendu,Adak, Mohini Mohan,Das, Sankar,Banerjee, Santa,Sengupta, Saumitra

, p. 34 - 37 (2007/10/02)

Methyl 2-,3-,4-carboxyphenylacetate and methyl 2-,3-,4-carboxyphenoxyacetate have been prepared through selective esterification of the aliphatic carboxylic acid function of the corresponding dicarboxylic acids using a mixture of phosphorus pentoxide (1 part), anhydrous copper sulphate (5 parts) and anhydrous sodium sulphate (5 parts).All the isomeric half-esters have been prepared through partial hydrolysis of the corresponding dimethylesters.

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