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2-ISOQUINOLIN-1-YL-2-METHYLPROPIONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81039-16-9

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81039-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81039-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,3 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81039-16:
(7*8)+(6*1)+(5*0)+(4*3)+(3*9)+(2*1)+(1*6)=109
109 % 10 = 9
So 81039-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2/c1-13(2,9-14)12-11-6-4-3-5-10(11)7-8-15-12/h3-8H,1-2H3

81039-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-isoquinolin-1-yl-2-methylpropanenitrile

1.2 Other means of identification

Product number -
Other names 1-(1-cyano-1-methylethyl)isoquinoline

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:81039-16-9 SDS

81039-16-9Downstream Products

81039-16-9Relevant academic research and scientific papers

Mild and practical method for the α-arylation of nitriles with heteroaryl halides

Klapars, Artis,Waldman, Jacob H.,Campos, Kevin R.,Jensen, Mark S.,McLaughlin, Mark,Chung, John Y. L.,Cvetovich, Raymond J.,Chen, Cheng-Yi

, p. 10186 - 10189 (2007/10/03)

A mild and transition-metal-free method for theα-arylation of a liphatic nitriles with activated heteroaryl halides was developed using NaHMDS o r KHMDS as base at ambient temperature. The key to the success of this method is generation of the nitrile anion in the presence of the heteroaryl halide. The method is applicable to both primary and secondary carbonitriles and a wide range of heteroaryl halides. Selective monoarylation was observed with primary carbonitriles. The operational simplicity and the mild reaction conditions add to the value of this methodas a practical alternative to the preparation of α-heteroaryl carbonitriles.

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