N-(Phenylacetyl)benzamide

Base Information

Chemical Name:N-(Phenylacetyl)benzamide
CAS No.:14072-62-9
Molecular Formula:C15H13NO2
Molecular Weight:239.274
Hs Code.:
DSSTox Substance ID:DTXSID80504637
Nikkaji Number:J2.395.951H
Wikidata:Q82359274

Synonyms:N-(Phenylacetyl)benzamide;14072-62-9;N-phenylacetylbenzamide;SCHEMBL1569112;DTXSID80504637

Suppliers and Price of N-(Phenylacetyl)benzamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of N-(Phenylacetyl)benzamide

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:239.094628657
Heavy Atom Count:18
Complexity:289

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC(=O)NC(=O)C2=CC=CC=C2

Technology Process of N-(Phenylacetyl)benzamide

There total 22 articles about N-(Phenylacetyl)benzamide 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: 86.0%

: 5874-61-3,21453-79-2,51127-19-6,75658-67-2
4-benzyl-2-phenyl-2-oxazolin-5-one

: 14072-62-9
N-(2-phenylacetyl)benzamide

Guidance literature:: With potassium tert-butylate; In dimethyl sulfoxide; at 0 ℃; for 2h;

Reference yield: 70.0%

: 7500-45-0
N-benzylphenylacetamide

: 14072-62-9
N-(2-phenylacetyl)benzamide

Guidance literature:: With tert.-butylhydroperoxide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; copper(I) bromide; In water; acetonitrile; at 20 ℃; for 8h;
DOI:10.1002/cjoc.201500190