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53369-76-9

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53369-76-9 Usage

Member of the benzonitrile class of compounds

This means that the compound is part of a larger group of similar compounds that are commonly used in the production of pharmaceuticals, dyes, and other industrial chemicals.

Derivative of benzonitrile with a dimethylaminomethyl group attached to the benzene ring

This describes the specific structure of the compound, which is based on a benzonitrile molecule with a dimethylaminomethyl group added to it.

Commonly used as a reagent in organic synthesis

This means that the compound is often used in chemical reactions to help produce other compounds.

Building block for the production of other complex organic compounds

This indicates that the compound is a key ingredient in the creation of more complex organic molecules.

Suitable for a wide range of applications in the chemical and pharmaceutical industries

This means that the compound has a variety of uses in different areas of these industries, thanks to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 53369-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,6 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53369-76:
(7*5)+(6*3)+(5*3)+(4*6)+(3*9)+(2*7)+(1*6)=139
139 % 10 = 9
So 53369-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2/c1-12(2)8-10-6-4-3-5-9(10)7-11/h3-6H,8H2,1-2H3/p+1

53369-76-9SDS

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-[(DIMETHYLAMINO)METHYL]BENZONITRILE

1.2 Other means of identification

Product number -
Other names 2-(dimethylaminomethyl)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:53369-76-9 SDS

53369-76-9Relevant articles and documents

Asymmetric Sommelet-Hauser rearrangement of N-benzylic ammonium salts

Tayama, Eiji,Kimura, Hiroshi

, p. 8869 - 8871 (2008/09/19)

(Chemical Equation Presented) [2,3] over [1,2]: The asymmetric Sommelet-Hauser rearrangement of an ammonium salt derived from N-benzylic proline-derived or N-benzylic glycine (-)-8-phenylmenthol ester is shown to proceed with remarkably high levels of stereoselectivity. The method provides unique and efficient access to optically active α-aryl amino acid derivatives.

Anellated 2,4-benzodiazepines, I

Mohrle,Lessel

, p. 367 - 372 (2007/10/02)

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15N and 13C NMR studies on cyclopalladated complexes. Synthetic palladium cyanide chemistry leading to organic nitriles

Affolter, Samuel,Pregosin, Paul S.

, p. 197 - 204 (2007/10/02)

15N NMR spectroscopy has been used to determine whether the 15NO group is coordinated in the cyclopalladated nitrosoamine complex 2, PdCl and K2, 11, as well as in several platinum

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