Ethyl 7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate

Base Information

Chemical Name:Ethyl 7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate
CAS No.:132272-52-7
Molecular Formula:C₁₁H₁₁N₃O₄
Molecular Weight:249.226
Hs Code.:
DSSTox Substance ID:DTXSID20563687
Nikkaji Number:J343.867H
Wikidata:Q82448167

Synonyms:132272-52-7;Ethyl 7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate;Ethyl 7-methyl-8-nitroimidazo-[1,2-a]pyridine-2-carboxylate;DTXSID20563687;7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylic acid ethyl ester;Ethyl7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate

Suppliers and Price of Ethyl 7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Matrix Scientific
Ethyl 7-methyl-8-nitroimidazo-[1,2-a]pyridine-2-carboxylate 97%
1g
$ 414.00

Crysdot
Ethyl7-methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate 95+%
5g
$ 769.00

Chemenu
Ethyl7-methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate 95%
5g
$ 726.00

Chemcia Scientific
7-Methyl-8-nitro-imidazo[1,2-a]pyridine-2-carboxylicacidethylester 95%
1 G
$ 250.00

Atlantic Research Chemicals
Ethyl7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate 95%
1gm:
$ 159.06

Total 1 raw suppliers

Chemical Property of Ethyl 7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:249.07495584
Heavy Atom Count:18
Complexity:344

Purity/Quality:: Ethyl 7-methyl-8-nitroimidazo-[1,2-a]pyridine-2-carboxylate 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)C1=CN2C=CC(=C(C2=N1)[N+](=O)[O-])C

Technology Process of Ethyl 7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate

There total 1 articles about Ethyl 7-Methyl-8-nitroimidazo[1,2-a]pyridine-2-carboxylate 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: 92.0%