2-phenyl-N-propylacetamide

Base Information

Chemical Name:2-phenyl-N-propylacetamide
CAS No.:64075-36-1
Molecular Formula:C11H15NO
Molecular Weight:177.246
Hs Code.:
DSSTox Substance ID:DTXSID60389388
Nikkaji Number:J2.725.809C
Wikidata:Q82185143

Synonyms:2-phenyl-N-propylacetamide;2-Phenyl-N-propyl-acetamide;64075-36-1;N-Propylbenzeneacetamide;Phenylacetamide, N-propyl-;SCHEMBL1927410;DTXSID60389388;AKOS003850635

Suppliers and Price of 2-phenyl-N-propylacetamide

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-phenyl-N-propylacetamide

Chemical Property:

PSA：32.59000
LogP:2.59560
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:177.115364102
Heavy Atom Count:13
Complexity:150

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCNC(=O)CC1=CC=CC=C1

Technology Process of 2-phenyl-N-propylacetamide

There total 13 articles about 2-phenyl-N-propylacetamide 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: 99.0%

: 107-10-8,42939-71-9
propylamine

: 101-41-7
benzeneacetic acid methyl ester

: 64075-36-1
N-(n-propyl)phenylacetamide

Guidance literature:: With ammonium nitrate; In neat (no solvent); at 20 ℃; for 12h; Green chemistry;
DOI:10.1246/cl.140846

Reference yield: 85.0%

: 107-10-8,42939-71-9
propylamine

: 101-94-0
p-tolyl phenylacetate

: 64075-36-1
N-(n-propyl)phenylacetamide

Guidance literature:: With tetra-(n-butyl)ammonium iodide; In dichloromethane; Ambient temperature; electrolyzed at -1.7 V at 50 mA;
DOI:10.1016/S0040-4039(00)95750-2

Reference yield: 75.0%

: 1-(azetidin-1-yl)-2-phenylethan-1-one

: 64075-36-1
N-(n-propyl)phenylacetamide

Guidance literature:: With 15-crown-5; sodium; In tetrahydrofuran; mineral oil; at 0 ℃; for 2h; chemoselective reaction; Inert atmosphere;
DOI:10.3390/molecules24030459