2(1H)-Pyridinone, 4-(4-nitrophenyl)-6-phenyl-

Base Information

Chemical Name:2(1H)-Pyridinone, 4-(4-nitrophenyl)-6-phenyl-
CAS No.:131081-22-6
Molecular Formula:C17H12N2O3
Molecular Weight:292.294
Hs Code.:
DSSTox Substance ID:DTXSID60440488
Nikkaji Number:J902.654A
Wikidata:Q82256813

Synonyms:2(1H)-Pyridinone, 4-(4-nitrophenyl)-6-phenyl-;131081-22-6;SCHEMBL8986954;DTXSID60440488;4-(4-Nitrophenyl)-6-phenylpyridin-2(1H)-one

Suppliers and Price of 2(1H)-Pyridinone, 4-(4-nitrophenyl)-6-phenyl-

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 1 raw suppliers

Chemical Property of 2(1H)-Pyridinone, 4-(4-nitrophenyl)-6-phenyl-

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:292.08479225
Heavy Atom Count:22
Complexity:505

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC(=CC(=O)N2)C3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of 2(1H)-Pyridinone, 4-(4-nitrophenyl)-6-phenyl-

There total 6 articles about 2(1H)-Pyridinone, 4-(4-nitrophenyl)-6-phenyl- 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: 69.0%

: 2960-55-6
(E)-3-(4-nitrophenyl)-1-phenylprop-2-en-1-one

: 49639-34-1,90617-28-0
phenylsulfinylacetic acid amide

: 131081-22-6
4-(4-nitrophenyl)-6-phenylpyridin-2(1H)-one

Guidance literature:: (E)-3-(4-nitrophenyl)-1-phenylprop-2-en-1-one; phenylsulfinylacetic acid amide; With 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride; In acetonitrile; at 50 ℃; for 4h; Inert atmosphere;

With acetic acid; In acetonitrile; for 3h; Inert atmosphere; Reflux;
DOI:10.1021/ol500162b

Reference yield: 57.0%

: 2960-55-6
(E)-3-(4-nitrophenyl)-1-phenylprop-2-en-1-one

: 69218-56-0
2-(1H-benzo[d][1,2,3]-triazol-1-yl)acetamide

: 131081-22-6
4-(4-nitrophenyl)-6-phenylpyridin-2(1H)-one

Guidance literature:: With sodium hydroxide; In ethanol; for 6h; Heating;
DOI:10.1021/jo970561h

Reference yield:

: C₂₃H₂₀N₂O₅S

: 131081-22-6
4-(4-nitrophenyl)-6-phenylpyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / acetonitrile / Inert atmosphere; Reflux

2: acetic acid / acetonitrile / Inert atmosphere; Reflux

With acetic acid; In acetonitrile;
DOI:10.1021/ol303320c