Imidazo(1,2-a)pyridine-3-acetonitrile, 7-methyl-

Base Information

• Chemical Name: Imidazo(1,2-a)pyridine-3-acetonitrile, 7-methyl-
• CAS No.: 17745-00-5
• Molecular Formula: C₁₀H₉N₃
• Molecular Weight: 171.202
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID20170310
• Wikidata: Q83040222
• Mol file: 17745-00-5.mol

Synonyms:Imidazo(1,2-a)pyridine-3-acetonitrile, 7-methyl-;2-(8-methylimidazo[1,2-a]pyridin-3-yl)acetonitrile;BRN 0779626;imidazo[1,2-a]pyridine-3-acetonitrile,8-methyl-;Imidazo(1,2-a)pyridine, 3-cyanomethyl-7-methyl-;DTXSID20170310;958782-93-9;Imidazo[1,2-a]pyridine-3-acetonitrile,7-methyl-

Chemical Property of Imidazo(1,2-a)pyridine-3-acetonitrile, 7-methyl-

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 41.09000
• Density: 1.15g/cm³
• LogP: 1.70878
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 171.079647300
• Heavy Atom Count: 13
• Complexity: 230

Purity/Quality:

99%min ^*data from raw suppliers

3-CYANOMETHYL-7-METHYLIMIDAZO(1,2-A)PYRIDINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=CN2C1=NC=C2CC#N

Technology Process of Imidazo(1,2-a)pyridine-3-acetonitrile, 7-methyl-

There total 1 articles about Imidazo(1,2-a)pyridine-3-acetonitrile, 7-methyl- 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:

→ 7-Methyl-3-cyanmethyl-imidazo<1.2-a>pyridin (17745-00-5)

Guidance literature:

3-Dimethylaminomethyl-7-methyl-imidazo<1.2-a>pyridin*CH3I, NaBH4, NaCN;

DOI:10.1021/jm00301a031