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Ethanone, 2-bromo-2-chloro-1-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96222-32-1

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96222-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96222-32-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,2 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96222-32:
(7*9)+(6*6)+(5*2)+(4*2)+(3*2)+(2*3)+(1*2)=131
131 % 10 = 1
So 96222-32-1 is a valid CAS Registry Number.

96222-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-2-chloro-1-(4-methylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2-bromo-2-chloro-1-p-tolyl-ethanone

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:96222-32-1 SDS

96222-32-1Upstream product

96222-32-1Downstream Products

96222-32-1Relevant academic research and scientific papers

Facile Approach to Geminal HeterodihalogenationOne-Pot Synthesis of α-Bromo-α-Chloro Ketones

Bian, Ming,Tang, Dong-Min,Zhou, Jin-Feng

, (2020)

An efficient and practical protocol for the geminal heterodihalogenation of methyl ketones by using readily available dimethyl sulfoxide and a combination of HCl and HBr is reported. Control experiments suggested that the acidity of the solution, as well as the oxidizing ability and nucleophilicity of the dimethyl sulfoxide might work cooperatively in ensuring the success of the tandem substitution. Its operational simplicity, easy accessibility, and mild oxidative conditions suggest that the present strategy might be useful for the assembly of bromochloromethyl functional groups in drug discovery.

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