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96717-76-9

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96717-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96717-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,1 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96717-76:
(7*9)+(6*6)+(5*7)+(4*1)+(3*7)+(2*7)+(1*6)=179
179 % 10 = 9
So 96717-76-9 is a valid CAS Registry Number.

96717-76-9SDS

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 1-(3-bromophenyl)-2,2-dichloroethanone

1.2 Other means of identification

Product number -
Other names 1-m-bromophenyl-2,2-dichloro-1-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:96717-76-9 SDS

96717-76-9Upstream product

96717-76-9Downstream Products

96717-76-9Relevant articles and documents

Halogenation Using Quaternary Ammonium Polyhalides. XXXII. Dichlorination of Aromatic Acetyl Derivatives with Benzyltrimethylammonium Tetrachloroiodate

Kakinami, Takaaki,Urabe, Yasuaki,Hermawan, Irwan,Yamanishi, Hiroko,Okamoto, Tsuyoshi,Kajigaeshi, Shoji

, p. 2549 - 2551 (1992)

The reaction of aromatic acetyl derivatives with 2 molar amounts of benzyltrimethylammonium tetrachloroiodate in acetic acid at 70 deg C for several hours gave dichloroacetyl derivatives in good yields.

A convenient and efficient synthesis of 1-aryl-2,2-dichloroethanones

Terent'ev, Alexander O.,Khodykin, Sergey V.,Troitskii, Nikolay A.,Ogibin, Yuri N.,Nikishin, Gennady I.

, p. 2845 - 2848 (2007/10/03)

1-Arylethanones are readily chlorinated with an aqueous HCl-H 2O2 system using ethanol as a cosolvent. The reaction prceeds rapidly and results in selective conversion of 1-arylethanones into 1-aryl-2,2-dichloroethanones in yields of 48-89%, depending on the nature of the substituent in the aryl group.

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