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(3-Aminophenyl)pyridin-3-ylmethanone

Base Information
  • Chemical Name:(3-Aminophenyl)pyridin-3-ylmethanone
  • CAS No.:79568-06-2
  • Molecular Formula:C12H10 N2 O
  • Molecular Weight:198.22
  • Hs Code.:
  • European Community (EC) Number:428-230-0
  • DSSTox Substance ID:DTXSID101288767
  • Mol file:79568-06-2.mol
(3-Aminophenyl)pyridin-3-ylmethanone

Synonyms:3-(3-Aminobenzoyl)pyridine;79568-06-2;(3-aminophenyl)pyridin-3-ylmethanone;(3-aminophenyl)-pyridin-3-ylmethanone;EC 428-230-0;3-AMINOPHENYL-3'-PYRYDYLKETON;SCHEMBL7085877;FOHMCNMHVRYMAK-UHFFFAOYSA-N;DTXSID101288767;(3-Aminophenyl)-3-pyridinylmethanone

Suppliers and Price of (3-Aminophenyl)pyridin-3-ylmethanone
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
Total 2 raw suppliers
Chemical Property of (3-Aminophenyl)pyridin-3-ylmethanone
Chemical Property:
  • Vapor Pressure:6.18E-07mmHg at 25°C 
  • Refractive Index:1.634 
  • Boiling Point:410.1°C at 760 mmHg 
  • Flash Point:201.8°C 
  • PSA:55.98000 
  • Density:1.215g/cm3 
  • LogP:2.47600 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:198.079312947
  • Heavy Atom Count:15
  • Complexity:230
Purity/Quality:

99.9% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC(=C1)N)C(=O)C2=CN=CC=C2
Technology Process of (3-Aminophenyl)pyridin-3-ylmethanone

There total 2 articles about (3-Aminophenyl)pyridin-3-ylmethanone 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 hydrogenchloride; tin(ll) chloride;
DOI:10.1021/jm00144a025
Guidance literature:
Multi-step reaction with 2 steps
1: 78 percent / HNO3, 97percent H2SO4 / 4 h / Ambient temperature
2: 40 percent / H2 / 5percent Pd/C / ethanol / 20 h
With sulfuric acid; hydrogen; nitric acid; palladium on activated charcoal; In ethanol;
DOI:10.1111/j.1751-1097.1996.tb09632.x
Guidance literature:
With tetrafluoroboric acid; sodium nitrite; In tetrahydrofuran; water; at -10 ℃; for 0.5h;
DOI:10.1021/jm00144a025
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