2-(2-Cyanoethyl)benzonitrile

Base Information

• Chemical Name: 2-(2-Cyanoethyl)benzonitrile
• CAS No.: 18328-00-2
• Molecular Formula: C10H8N2
• Molecular Weight: 156.187
• DSSTox Substance ID: DTXSID50472753
• Nikkaji Number: J1.425.432C
• Wikidata: Q82301873
• Mol file: 18328-00-2.mol

Synonyms:2-(2-cyanoethyl)benzonitrile;18328-00-2;Benzenepropanenitrile, 2-cyano-;(2-Cyanophenyl)propanenitrile;2-(2-cyanoethyl)-benzonitrile;SCHEMBL11337847;DTXSID50472753;EN300-1849532

Chemical Property of 2-(2-Cyanoethyl)benzonitrile

Chemical Property:

• XLogP3: 1.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 156.068748264
• Heavy Atom Count: 12
• Complexity: 227

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)CCC#N)C#N

Technology Process of 2-(2-Cyanoethyl)benzonitrile

There total 5 articles about 2-(2-Cyanoethyl)benzonitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 72.0%

2-(2-bromo-benzyl)-malononitrile → 3-(2-cyano-phenyl)-propionitrile (18328-00-2)

Guidance literature:

With azobis(2-cyanobutane); tri-n-butyl-tin hydride; In cyclohexane; for 9h; Heating;

DOI:10.1016/S0040-4039(00)01596-3

Reference yield: 44.0%

2-(bromomethyl)benzonitrile (22115-41-9) + cyanomethyl bromide (590-17-0) → 3-(2-cyano-phenyl)-propionitrile (18328-00-2)

Guidance literature:

With nickel; In 1,2-dimethoxyethane; at 85 ℃; for 0.25h;

DOI:10.1055/s-1984-30990

Reference yield:

(+/-)-3t-(cis-2-cyano-cyclohex-3-enyl)-acrylonitrile (24532-97-6,63783-44-8,63783-45-9,98920-01-5,121960-59-6) → 3-(2-cyano-phenyl)-propionitrile (18328-00-2)

Guidance literature:

With N-Bromosuccinimide; benzene; Erhitzen des Reaktionsprodukts mit Isochinolin auf 180-190grad;

DOI:10.1021/ja01172a072

upstream raw materials:

N-Bromosuccinimide

(+/-)-3t-(cis-2-cyano-cyclohex-3-enyl)-acrylonitrile

benzene

2-(bromomethyl)benzonitrile

Downstream raw materials:

2-(2-carboxyethyl)benzoic acid

3-<2-Hydroxyamidino-phenyl>-propionsaeureamidoxim