N-(4-methylphenyl)-3-phenylpropanamide

Base Information

Chemical Name:N-(4-methylphenyl)-3-phenylpropanamide
CAS No.:71231-25-9
Molecular Formula:C16H17NO
Molecular Weight:239.317
Hs Code.:
DSSTox Substance ID:DTXSID50354686
Nikkaji Number:J2.521.446C
Wikidata:Q82132995

Synonyms:N-(4-methylphenyl)-3-phenylpropanamide;71231-25-9;3-phenyl-N-(p-tolyl)propanamide;Benzenepropanamide, N-(4-methylphenyl)-;CBDivE_001932;Cambridge id 5104249;SCHEMBL1471759;DTXSID50354686;STL387969;AKOS002953310;EN300-240222;SR-01000195214;SR-01000195214-1;F3147-1549

Suppliers and Price of N-(4-methylphenyl)-3-phenylpropanamide

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 3 raw suppliers

Chemical Property of N-(4-methylphenyl)-3-phenylpropanamide

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:239.131014166
Heavy Atom Count:18
Complexity:250

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)NC(=O)CCC2=CC=CC=C2

Technology Process of N-(4-methylphenyl)-3-phenylpropanamide

There total 15 articles about N-(4-methylphenyl)-3-phenylpropanamide 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: 97.0%

: 103-89-9
4-Methylacetanilide

: 100-51-6,185532-71-2
benzyl alcohol

: 71231-25-9
N-(4-methylphenyl)-3-phenylpropanamide

Guidance literature:: With tri-tert-butyl phosphine; potassium tert-butylate; nickel diacetate; In 1,4-dioxane; toluene; at 80 ℃; for 12h; Inert atmosphere; Glovebox; Schlenk technique;
DOI:10.1039/d0cc06468h