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55676-84-1

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55676-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55676-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,7 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55676-84:
(7*5)+(6*5)+(5*6)+(4*7)+(3*6)+(2*8)+(1*4)=161
161 % 10 = 1
So 55676-84-1 is a valid CAS Registry Number.

55676-84-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-4-chloro-1-methylbenzene

1.2 Other means of identification

Product number -
Other names 2-benzyl-4-chlorotoluene

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:55676-84-1 SDS

55676-84-1Downstream Products

55676-84-1Relevant articles and documents

Iron-catalyzed benzylation reaction of arenes with benzyl thiocyanates

Guo, Xiao-Kang,Zhao, Dong-Yun,Li, Jin-Heng,Zhang, Xing-Guo,Deng, Chen-Liang,Tang, Ri-Yuan

supporting information; experimental part, p. 627 - 631 (2012/03/27)

A novel, regioselective protocol for the synthesis of diphenylmethane derivatives has been developed by using iron-catalyzed Friedel-Crafts reaction of arenes with benzyl thiocyanates. In the presence of FeBr3, a variety of benzyl thiocyanates underwent the reaction with arenes to selectively afford the corresponding diarylmethane derivatives in moderate to high yields. Georg Thieme Verlag Stuttgart · New York.

Manufacture of o-benzyltoluenes

-

, (2008/06/13)

The manufacture of o-benzyltoluenes by reaction of o-xylyl halides with benzenes in the presence of boron trifluoride or its derivatives, and new o-benzyltoluenes. The new and known o-benzyltoluenes I manufactured by the process of the invention are starting materials for the manufacture of anthracene and anthraquinone and their derivatives.

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