o-Phenethyl-N-acetylaniline

Base Information Edit

Chemical Name:o-Phenethyl-N-acetylaniline
CAS No.:54888-53-8
Molecular Formula:C16H17NO
Molecular Weight:239.31200
Hs Code.:
Mol file:54888-53-8.mol

Synonyms:N-Bibenzyl-2-yl-acetamid;2-Acetamino-bibenzyl;N-bibenzyl-2-yl-acetamide;N-(2-Phenethyl-phenyl)-acetamide;

Suppliers and Price of o-Phenethyl-N-acetylaniline

Supply Marketing:Edit

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 4 raw suppliers

Chemical Property of o-Phenethyl-N-acetylaniline Edit

Chemical Property:

Melting Point:98 °C
Boiling Point:408.2±24.0 °C(Predicted)
PKA:15.07±0.70(Predicted)
PSA：29.10000
Density:1.107±0.06 g/cm3(Predicted)
LogP:3.50320

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of o-Phenethyl-N-acetylaniline

There total 7 articles about o-Phenethyl-N-acetylaniline 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: 85.0%

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

: 103-84-4
Acetanilid

: 54888-53-8
2-acetamidobibenzyl

: N-(2-(1-phenylethyl)phenyl)acetamide

Guidance literature:: With [Ir(1,5-cyclooctadiene)₂]triflate; 1,4-bis[bis(pentafluorophenyl)phosphino]butane; In 1,4-dioxane; at 120 ℃; Reagent/catalyst; Solvent; Inert atmosphere; Sealed tube;
DOI:10.1002/anie.201506581

Reference yield:

: 4714-25-4
2-nitrostilbene

: 54888-53-8
2-acetamidobibenzyl

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / hydrazine hydrate / nickel / ethanol

2: Raney nickel / ethanol / 0.5 h / Heating

With nickel; hydrazine hydrate; nickel; In ethanol;