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2-bromo-2,2-diphenylacetyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17397-37-4

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17397-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17397-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,9 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17397-37:
(7*1)+(6*7)+(5*3)+(4*9)+(3*7)+(2*3)+(1*7)=134
134 % 10 = 4
So 17397-37-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H10Br2O/c15-13(17)14(16,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H

17397-37-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-2,2-diphenylacetyl bromide

1.2 Other means of identification

Product number -
Other names Benzeneacetyl bromide, α-bromo-α-phenyl-

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:17397-37-4 SDS

17397-37-4Relevant academic research and scientific papers

Monoacyl Sulfates as Intermediates for α-Halogenation of Aliphatic Acids

Ogata, Yoshiro,Adachi, Koichi

, p. 1182 - 1184 (2007/10/02)

The mechanism of the α-halogenation of aliphatic carboxylic acids, promoted by ClSO3H or oleum, has been reexamined.Ketenes, which have been postulated as the intermediates in this halogenation, have been found to react with I2 much faster than a mixture of the corresponding acid and ClSO3H.Evidence is presented to support the hypothesis that the halogenation proceeds through the cyclic enol form of the monoacyl sulfate RR'CHCO2SO3H (3) rather than through the ketene.

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