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2-Propanol, 1-bromo-3-chloro-, benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102495-72-7

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102495-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102495-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,9 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102495-72:
(8*1)+(7*0)+(6*2)+(5*4)+(4*9)+(3*5)+(2*7)+(1*2)=107
107 % 10 = 7
So 102495-72-7 is a valid CAS Registry Number.

102495-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoic acid-(β-bromo-β'-chloro-isopropyl ester)

1.2 Other means of identification

Product number -
Other names Benzoic acid 2-bromo-1-chloromethyl-ethyl ester

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:102495-72-7 SDS

102495-72-7Downstream Products

102495-72-7Relevant academic research and scientific papers

One-pot synthesis of ω-bromoesters from aromatic aldehydes and diols using pyridinium hydrobromide perbromide

Aoyama, Tadashi,Takido, Toshio,Kodomari, Mitsuo

, p. 1989 - 1992 (2007/10/03)

A simple and efficient one-pot procedure has been developed for the synthesis of ω-bromoesters from aromatic aldehydes and diols in the presence of pyridinium hydrobromide perbromide (PHPB) and triethoxymethane in which aldehyde reacts first with diol and the product, cyclic acetal, reacts with PHPB to give the final product, ω-bromoesters.

Non-Catalyzed Cleavage Reactions of Ethers with Acyl Halides under High-Pressure Conditions

Kotsuki, Hiyoshizo,Ichikawa, Yoshikatsu,Nishizawa, Hitoshi

, p. 673 - 676 (2007/10/02)

Various cyclic and acyclic ethers are efficiently cleaved with acyl chlorides or bromides to give ω-chloro- or ω-bromoesters under high-pressure conditions.

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