2-Methyl-3-nitroimidazo[1,2-a]pyridine

Base Information

• Chemical Name: 2-Methyl-3-nitroimidazo[1,2-a]pyridine
• CAS No.: 34165-09-8
• Molecular Formula: C₈H₇N₃O₂
• Molecular Weight: 177.162
• Hs Code.: 2933990090
• ChEMBL ID: CHEMBL2441873
• DSSTox Substance ID: DTXSID10491844
• Nikkaji Number: J1.615.166A
• Wikidata: Q82336899
• Mol file: 34165-09-8.mol

Synonyms:2-Methyl-3-nitroimidazo[1,2-a]pyridine;34165-09-8;SCHEMBL6739461;CHEMBL2441873;DTXSID10491844;MFCD09800612;AKOS006329478;DS-5011;CS-0153430

Chemical Property of 2-Methyl-3-nitroimidazo[1,2-a]pyridine

Chemical Property:

• PSA: 63.12000
• LogP: 2.07410
• Storage Temp.: 2-8°C
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 177.053826475
• Heavy Atom Count: 13
• Complexity: 216

Purity/Quality:

97% ^*data from raw suppliers

2-Methyl-3-nitroimidazo[1,2-a]pyridine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(N2C=CC=CC2=N1)[N+](=O)[O-]

Technology Process of 2-Methyl-3-nitroimidazo[1,2-a]pyridine

There total 2 articles about 2-Methyl-3-nitroimidazo[1,2-a]pyridine 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: 90.0%

2-methylimidazo[1,2-a]pyridine (934-37-2) → 2-methyl-3-nitroimidazo[1,2-a]pyridine (34165-09-8)

Guidance literature:

With sulfuric acid; nitric acid; at 20 ℃;

DOI:10.1016/j.bmc.2013.09.002

Reference yield:

→ 2-methyl-3-nitroimidazo[1,2-a]pyridine (34165-09-8)

Guidance literature:

2-Methylimidazo<1,2-a>pyridin, HNO3, H2SO4;

Reference yield: 95.0%

2-methyl-3-nitroimidazo[1,2-a]pyridine (34165-09-8) → 3-amino-2-methylimidazo[1,2-a]pyridine (28036-31-9)

Guidance literature:

With palladium 10% on activated carbon; hydrogen; In ethanol; for 18h;

upstream raw materials:

2-methylimidazo[1,2-a]pyridine

Downstream raw materials:

3-amino-2-methylimidazo[1,2-a]pyridine

3-nitro-imidazo[1,2-a]pyridine

3-nitroimidazo[1,2-a]pyridine-2-carbaldehyde

3-amino-2-formylimidazo[1,2-a]pyridine