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696-61-7

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696-61-7 Usage

Chemical Properties

Dark colored solution

Check Digit Verification of cas no

The CAS Registry Mumber 696-61-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 696-61:
(5*6)+(4*9)+(3*6)+(2*6)+(1*1)=97
97 % 10 = 7
So 696-61-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H7.ClH.Mg/c1-7-5-3-2-4-6-7;;/h3-6H,1H3;1H;/q;;+1/p-1/rC7H7ClMg/c1-6-2-4-7(9-8)5-3-6/h2-5H,1H3

696-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name p-Tolylmagnesium chloride

1.2 Other means of identification

Product number -
Other names magnesium,methylbenzene,chloride

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:696-61-7 SDS

696-61-7Relevant articles and documents

Manganese-catalyzed oxidative homo-coupling of aryl Grignard chlorides

Zhou, Zhiming,Xue, Weizhe

supporting information; experimental part, p. 599 - 603 (2009/05/30)

Manganese-catalyzed homo-coupling of aryl magnesium chlorides to give biphenyls was successfully achieved using manganese chloride as catalyst. A variety of aryl magnesium chlorides were efficiently converted into the corresponding symmetrical biaryls using 10 mol% MnCl2 as catalyst in the presence of a stoichiometric amount of 1,2-dichloroethane. Since the aryl chlorides, from which the Grignard reagents were prepared, are cheaper and more readily available that the corresponding bromides and iodides this procedure should become the method of choice for preparing symmetrical biaryls.

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