Cyanomethyl radical

Base Information

• Chemical Name: Cyanomethyl radical
• CAS No.: 2932-82-3
• Molecular Formula: C₂H₂N
• Molecular Weight: 40.0446
• DSSTox Substance ID: DTXSID20183561
• Nikkaji Number: J371.061K
• Mol file: 2932-82-3.mol

Synonyms:Cyanomethyl radical;2932-82-3;CH2CN;DTXSID20183561

Chemical Property of Cyanomethyl radical

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 0.00000
• Density: g/cm³
• LogP: -0.35780
• XLogP3: 0
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 40.018724068
• Heavy Atom Count: 3
• Complexity: 29.3

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: [CH2]C#N

Technology Process of Cyanomethyl radical

There total 5 articles about Cyanomethyl radical 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:

tert-butoxy radical (3141-58-0) + acetonitrile (75-05-8,26809-02-9) → cyanomethyl (3744-26-1,2932-82-3) + tert-butyl alcohol (75-65-0)

Guidance literature:

at 25.85 ℃; Kinetics;

DOI:10.1016/j.cplett.2006.06.100

Reference yield:

iodoacetonitrile (624-75-9) + octan-1-yl radical (4606-96-6) → 1-Iodooctane (629-27-6) + cyanomethyl (3744-26-1,2932-82-3)

Guidance literature:

In benzene; at 50 ℃; Rate constant;

DOI:10.1021/jo00269a016

Reference yield:

C9H8NO2 → cyanomethyl (3744-26-1,2932-82-3) + benzoic acid (65-85-0,8013-63-6)

Guidance literature:

In various solvent(s); at 26.84 ℃; Further Variations:; Temperatures; Kinetics;

DOI:10.1039/b104859g

upstream raw materials:

iodoacetonitrile

octan-1-yl radical

C₆H₅N₂⁽¹⁺⁾*CNS^(1-)

tert-butoxy radical

Downstream raw materials:

acetonitrile

formaldehyd

glyoxylonitrile

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