N-(3-cyanophenyl)-2-phenylacetamide

Base Information

Chemical Name:N-(3-cyanophenyl)-2-phenylacetamide
CAS No.:89246-40-2
Molecular Formula:C15H12N2O
Molecular Weight:236.273
Hs Code.:
DSSTox Substance ID:DTXSID00352591
Nikkaji Number:J1.588.322G
Wikidata:Q82129829
ChEMBL ID:CHEMBL215684
Mol file:89246-40-2.mol

Synonyms:N-(3-cyanophenyl)-2-phenylacetamide;89246-40-2;Oprea1_051374;Oprea1_357948;MLS000684027;CHEMBL215684;DTXSID00352591;HMS1586G06;HMS2740L14;STK017167;AKOS000174022;SMR000291660;AN-329/40892422;SR-01000233250;SR-01000233250-1;Z26548145

Suppliers and Price of N-(3-cyanophenyl)-2-phenylacetamide

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
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price

Aronis compounds
N-(3-cyanophenyl)-2-phenylacetamide
1mg
$ 12.00

Total 0 raw suppliers

Chemical Property of N-(3-cyanophenyl)-2-phenylacetamide

Chemical Property:

PSA：56.38000
LogP:3.38898
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:236.094963011
Heavy Atom Count:18
Complexity:325

Purity/Quality:: N-(3-cyanophenyl)-2-phenylacetamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC(=O)NC2=CC=CC(=C2)C#N
Uses N-(3-Cyanophenyl)benzeneacetamide is a pharmaceutically relevant amide and an effective inhibitor of morbillivirus-induced membrane fusion with low cytotoxicity

Technology Process of N-(3-cyanophenyl)-2-phenylacetamide

There total 3 articles about N-(3-cyanophenyl)-2-phenylacetamide 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: 75.0%

: 2237-30-1
m-cyanoaniline

: 103-80-0
phenylacetyl chloride

: 89246-40-2
N-(3-cyanophenyl)-2-phenylacetamide

Guidance literature:: m-cyanoaniline; With sodium hydrogencarbonate; In chloroform; at 20 ℃; for 0.166667h;

phenylacetyl chloride; In chloroform; for 2h;
DOI:10.1021/jm0602559

Reference yield: 57.0%

: 201230-82-2
carbon monoxide

: 108-88-3,15644-74-3,16713-13-6
toluene

: 2237-30-1
m-cyanoaniline

: 89246-40-2
N-(3-cyanophenyl)-2-phenylacetamide

Guidance literature:: With di-tert-butyl peroxide; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; palladium dichloride; at 125 ℃; for 24h; under 38002.6 Torr; Autoclave;
DOI:10.1039/c3cc47015f