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1373917-20-4

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1373917-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373917-20-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,9,1 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1373917-20:
(9*1)+(8*3)+(7*7)+(6*3)+(5*9)+(4*1)+(3*7)+(2*2)+(1*0)=174
174 % 10 = 4
So 1373917-20-4 is a valid CAS Registry Number.

1373917-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-2-pyrimidin-2-ylbenzonitrile

1.2 Other means of identification

Product number -
Other names 4-methyl-2-(pyrimidin-2-yl)benzonitrile

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:1373917-20-4 SDS

1373917-20-4Relevant articles and documents

α-Iminonitrile: A new cyanating agent for the palladium catalyzed C-H cyanation of arenes

Chen, Zhen-Bang,Zhang, Fang-Ling,Yuan, Qing,Chen, Hai-Fang,Zhu, Yong-Ming,Shen, Jing-Kang

, p. 64234 - 64238 (2016/07/23)

An efficient palladium-catalyzed C-H cyanation reaction of arenes using α-iminonitrile as a new cyanating reagent has been developed. With high regioselectivity and broad substrate scope, this reaction offers monocyanated products in moderate to excellent

Rhodium-catalyzed direct C-H bond cyanation of arenes with isocyanide

Hong, Xiaohu,Wang, Hao,Qian, Guangyin,Tan, Qitao,Xu, Bin

, p. 3228 - 3237 (2014/05/06)

An efficient rhodium-catalyzed regioselective C-H bond cyanation of arenes was developed using tert-butyl isocyanide as the cyanide source. A wide range of (hetero)aryl and cycloalkenyl nitriles could be afforded with high regioselectivity and good functional group tolerance.

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