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6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile

Base Information
  • Chemical Name:6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
  • CAS No.:82626-72-0
  • Molecular Formula:C15H9Cl2N3
  • Molecular Weight:302.163
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60517245
  • Nikkaji Number:J3.666.195J
  • Wikidata:Q82379140
  • Mol file:82626-72-0.mol
6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile

Synonyms:82626-72-0;6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile;2-[6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl]acetonitrile;2-(6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)acetonitrile;6-Chloro-2-(4-chlorophenyl)imidazo[1,2-alpha]pyridine-3-acetonitrile;SCHEMBL7995;DTXSID60517245;AKOS022235576;FT-0664661;[6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl]acetonitrile

Suppliers and Price of 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
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
  • TRC
  • 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
  • 25mg
  • $ 140.00
  • Medical Isotopes, Inc.
  • 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-α]pyridine-3-acetonitrile
  • 125 mg
  • $ 2120.00
  • Biosynth Carbosynth
  • 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
  • 50 mg
  • $ 462.00
  • Biosynth Carbosynth
  • 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
  • 25 mg
  • $ 254.50
  • Biosynth Carbosynth
  • 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
  • 10 mg
  • $ 139.80
  • Biosynth Carbosynth
  • 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
  • 250 mg
  • $ 1530.00
  • Biosynth Carbosynth
  • 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
  • 100 mg
  • $ 840.00
  • American Custom Chemicals Corporation
  • 6-CHLORO-2-(4-CHLOROPHENYL)IMIDAZO(1,2-A)PYRIDINE-3-ACETONITRILE 95.00%
  • 250MG
  • $ 1871.10
  • American Custom Chemicals Corporation
  • 6-CHLORO-2-(4-CHLOROPHENYL)IMIDAZO(1,2-A)PYRIDINE-3-ACETONITRILE 95.00%
  • 25MG
  • $ 739.20
  • AK Scientific
  • 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
  • 250mg
  • $ 2115.00
Total 4 raw suppliers
Chemical Property of 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile
Chemical Property:
  • XLogP3:4.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:301.0173527
  • Heavy Atom Count:20
  • Complexity:386
Purity/Quality:

98% *data from raw suppliers

6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC(=CC=C1C2=C(N3C=C(C=CC3=N2)Cl)CC#N)Cl
  • Uses An intermediate for the synthesis of Alpidem.
Technology Process of 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile

There total 8 articles about 6-Chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-acetonitrile 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:
Guidance literature:
With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Irradiation; Sealed tube; Inert atmosphere;
DOI:10.1055/a-1704-4822
Guidance literature:
With tris[2-phenylpyridinato-C2,N]iridium(III); N,N-dimethyl-formamide; at 24 ℃; regioselective reaction; Inert atmosphere; UV-irradiation;
DOI:10.1016/j.tet.2018.04.079
Guidance literature:
With fac-tris(2-phenylpyridinato-N,C2')iridium(III); sodium hydrogencarbonate; In dimethyl sulfoxide; at 20 ℃; for 12h; regioselective reaction; Schlenk technique; Inert atmosphere; Irradiation;
DOI:10.1021/acs.joc.7b00750
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