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Benzenepropanenitrile, also known as 2-cyano, is an organic compound with the chemical formula C9H7N. It is a colorless to pale yellow liquid with a characteristic odor. Benzenepropanenitrile, 2-cyano- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known as 2-phenylpropanenitrile or β-phenylpropionitrile. The molecule consists of a benzene ring attached to a propyl chain, with a nitrile group (CN) at the second carbon of the propyl chain. Due to its versatile chemical properties, 2-cyano is widely used in the production of various compounds, such as pharmaceuticals, dyes, and polymers.

18328-00-2

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18328-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18328-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,2 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18328-00:
(7*1)+(6*8)+(5*3)+(4*2)+(3*8)+(2*0)+(1*0)=102
102 % 10 = 2
So 18328-00-2 is a valid CAS Registry Number.

18328-00-2SDS

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-(2-cyanoethyl)benzonitrile

1.2 Other means of identification

Product number -
Other names Benzenepropanenitrile,2-cyano

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:18328-00-2 SDS

18328-00-2Relevant academic research and scientific papers

Radical cyclisation onto nitriles

Bowman,Bridge,Brookes

, p. 8989 - 8994 (2007/10/03)

Iminyl radicals, generated by 5-exo cyclisation of alkyl, vinyl and aryl C-centred radicals onto nitriles, undergo β-scission (nitrile translocation), reduction or tandem cyclisation onto alkenes depending on the nature of the α-substituent. 5-exo Cyclisations of aryl radicals onto nitriles undergo nitrile translocation when the α-substituent is CN, CO2R, SO2Ph or CONMe2. The rate of translocation is faster than 5- or 6-exo cyclisation onto alkenes or 1,5-hydrogen abstraction of allylic hydrogens. When the α-substituents are alkyl, the intermediate iminyl radicals do not undergo nitrile translocation. (C) 2000 Elsevier Science Ltd.

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