2-methyl-N-(1-phenylethyl)propanamide

Base Information

Chemical Name:2-methyl-N-(1-phenylethyl)propanamide
CAS No.:72924-95-9
Molecular Formula:C12H17NO
Molecular Weight:191.273
Hs Code.:
DSSTox Substance ID:DTXSID90392486
Mol file:72924-95-9.mol

Synonyms:2-methyl-N-(1-phenylethyl)propanamide;72924-95-9;Propanamide, 2-methyl-N-(1-phenylethyl)-;SCHEMBL7855088;DTXSID90392486;AKOS003871297;N-(1-PHENYL-ETHYL)-ISOBUTYRAMIDE;Z54930712

Suppliers and Price of 2-methyl-N-(1-phenylethyl)propanamide

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 1 raw suppliers

Chemical Property of 2-methyl-N-(1-phenylethyl)propanamide

Chemical Property:

PSA：32.59000
LogP:3.36010
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:191.131014166
Heavy Atom Count:14
Complexity:183

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2-methyl-N-(1-phenylethyl)propanamide

There total 6 articles about 2-methyl-N-(1-phenylethyl)propanamide 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: 89.0%

: 618-36-0
rac-methylbenzylamine

: 1821-12-1
4-Phenylbutyric acid

: 72924-95-9
N-(α-methylbenzyl)isobutyramide

: 98379-81-8
3-Methyl-but-2-enoic acid (1-phenyl-ethyl)-amide

: 19145-73-4,78172-89-1
N-(1-phenylethyl)hexanamide

: 78172-90-4
2-Naphthalen-1-yl-N-(1-phenyl-ethyl)-acetamide

: 75056-45-0
N-(1-phenylethyl)-4-phenylbutyramide

: 64528-63-8
N-(1-phenylethyl)pivalamide

Guidance literature:: With potassium hydroxide; bis(o-nitrophenyl)phenylphosphonate; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; other acids; multistep reaction;
DOI:10.1246/cl.1981.285

Reference yield: 79.0%

: 563-83-7
ISOPROPYLAMIDE

: 4545-21-5
acetophenone p-toluenesulfonylhydrazone

: 72924-95-9
N-(α-methylbenzyl)isobutyramide

Guidance literature:: With copper(l) iodide; tetra-(n-butyl)ammonium iodide; lithium tert-butoxide; In tetrahydrofuran; at 80 ℃; for 6h; Schlenk technique; Inert atmosphere;
DOI:10.1002/asia.201600733