2-(p-Aminophenyl)-N-(alpha-methylphenethyl)acetamide

Base Information

Chemical Name:2-(p-Aminophenyl)-N-(alpha-methylphenethyl)acetamide
CAS No.:2792-95-2
Molecular Formula:C₁₇H₂₀N₂O
Molecular Weight:268.359
Hs Code.:2924299090
DSSTox Substance ID:DTXSID60950597
Nikkaji Number:J13.020F
Mol file:2792-95-2.mol

Synonyms:fepracet;fepracet hydrochloride;IEM 366;phepracet;pheprazet

Suppliers and Price of 2-(p-Aminophenyl)-N-(alpha-methylphenethyl)acetamide

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

Matrix Scientific
2-(4-Aminophenyl)-N-(1-methyl-2-phenylethyl)acetamide hydrochloride
25g
$ 3000.00

Matrix Scientific
2-(4-Aminophenyl)-N-(1-methyl-2-phenylethyl)acetamide hydrochloride
10g
$ 1600.00

Matrix Scientific
2-(4-Aminophenyl)-N-(1-methyl-2-phenylethyl)acetamide hydrochloride
5g
$ 1000.00

Matrix Scientific
2-(4-Aminophenyl)-N-(1-methyl-2-phenylethyl)acetamide hydrochloride
1g
$ 300.00

Matrix Scientific
2-(4-Aminophenyl)-N-(1-methyl-2-phenylethyl)acetamide hydrochloride
0.500g
$ 240.00

Total 4 raw suppliers

Chemical Property of 2-(p-Aminophenyl)-N-(alpha-methylphenethyl)acetamide

Chemical Property:

Vapor Pressure:6.95E-11mmHg at 25°C
Boiling Point:519.2°C at 760 mmHg
Flash Point:267.8°C
PSA：58.61000
Density:1.113g/cm³
LogP:3.98020
XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:268.157563266
Heavy Atom Count:20
Complexity:291

Purity/Quality:

99% ^*data from raw suppliers

2-(4-Aminophenyl)-N-(1-methyl-2-phenylethyl)acetamide hydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CC1=CC=CC=C1)NC(=O)CC2=CC=C(C=C2)N

Technology Process of 2-(p-Aminophenyl)-N-(alpha-methylphenethyl)acetamide

There total 3 articles about 2-(p-Aminophenyl)-N-(alpha-methylphenethyl)acetamide 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:

: 1197-55-3
4-aminophenylacetic acid

: 2792-95-2
4-Aminophenylacetic acid β-phenylisopropylamide

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH

2: (i) DCC, CHCl₃, (ii) H₂, HCl, Pd-C, MeOH

With sodium hydroxide;
DOI:10.1021/jo01327a040