N-(2-acetylphenyl)-4-nitrobenzamide

Base Information

Chemical Name:N-(2-acetylphenyl)-4-nitrobenzamide
CAS No.:1742-15-0
Molecular Formula:C15H12N2O4
Molecular Weight:284.271
Hs Code.:
DSSTox Substance ID:DTXSID001292824
ChEMBL ID:CHEMBL3917910

Synonyms:CHEMBL3917910;N-(2-acetylphenyl)-4-nitrobenzamide;SCHEMBL7372951;DTXSID001292824;BDBM50199478;AKOS000185633;1742-15-0;Z27879744

Suppliers and Price of N-(2-acetylphenyl)-4-nitrobenzamide

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 N-(2-acetylphenyl)-4-nitrobenzamide

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:284.07970687
Heavy Atom Count:21
Complexity:410

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=CC=CC=C1NC(=O)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of N-(2-acetylphenyl)-4-nitrobenzamide

There total 1 articles about N-(2-acetylphenyl)-4-nitrobenzamide 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:

: 1742-15-0
N-(2-acetylphenyl)-4-nitrobenzamide

Guidance literature:: p-Nitrobenzoylchlorid, 2-Aminoacetophenon;

Reference yield: 89.0%

: 1742-15-0
N-(2-acetylphenyl)-4-nitrobenzamide

: 16063-05-1
2-(4-nitrophenyl)-4H-3,1-benzoxazin-4-one

Guidance literature:: N-(2-acetylphenyl)-4-nitrobenzamide; With iodine; sodium hydrogencarbonate; In dimethyl sulfoxide; at 20 ℃; for 0.0333333h;

With tert.-butylhydroperoxide; In nonane; dimethyl sulfoxide; at 95 ℃; for 3h;
DOI:10.1021/acs.orglett.6b02142

Reference yield: 65.0%

: 1742-15-0
N-(2-acetylphenyl)-4-nitrobenzamide

: 74-88-4
methyl iodide

: 1-methyl-2-(4-nitrophenyl)quinolin-4(1H)-one

Guidance literature:: N-(2-acetylphenyl)-4-nitrobenzamide; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 0.5h;

methyl iodide; In tetrahydrofuran;
DOI:10.1016/j.tet.2015.07.058