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135277-07-5

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135277-07-5 Usage

Chemical Classification

Nitrile

Structural Features

Contains a benzene ring and a pyrrolidine ring

Usage

Commonly used in pharmaceutical research and drug development
Primarily employed in the synthesis of various organic compounds

Potential Applications

Development of new drugs for various medical conditions

Industrial Uses

May have other industrial applications, although its main focus is in medicine and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 135277-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,7 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 135277-07:
(8*1)+(7*3)+(6*5)+(5*2)+(4*7)+(3*7)+(2*0)+(1*7)=125
125 % 10 = 5
So 135277-07-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2/c13-9-11-5-1-2-6-12(11)10-14-7-3-4-8-14/h1-2,5-6H,3-4,7-8,10H2

135277-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(PYRROLIDIN-1-YLMETHYL)BENZONITRILE

1.2 Other means of identification

Product number -
Other names Benzonitrile,2-(1-pyrrolidinylmethyl)

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:135277-07-5 SDS

135277-07-5Relevant articles and documents

tert-Butoxy-Radical-Promoted α-Arylation of Alkylamines with Aryl Halides

Ueno, Ryota,Ikeda, Yuko,Shirakawa, Eiji

supporting information, p. 4188 - 4193 (2017/08/07)

In the presence of a tert-butoxy radical precursor, the reaction of alkylamines with aryl halides was found to give α-arylated alkylamines through homolytic aromatic substitution of the halogen atoms.

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