Benzeneethanamine, alpha-methyl-N-(2-phenylethyl)-

Base Information

Chemical Name:Benzeneethanamine, alpha-methyl-N-(2-phenylethyl)-
CAS No.:21026-75-5
Molecular Formula:C17H21 N
Molecular Weight:239.36
Hs Code.:2921499090
DSSTox Substance ID:DTXSID00943322
Nikkaji Number:J99.841I
Mol file:21026-75-5.mol

Synonyms:IEM 570;IEM 570 hydrochloride;IEM 570, (+-)-isomer;IEM-570

Suppliers and Price of Benzeneethanamine, alpha-methyl-N-(2-phenylethyl)-

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 2 raw suppliers

Chemical Property of Benzeneethanamine, alpha-methyl-N-(2-phenylethyl)-

Chemical Property:

Vapor Pressure:1.94E-05mmHg at 25°C
Boiling Point:362.4°Cat760mmHg
Flash Point:168.8°C
PSA：12.03000
Density:g/cm³
LogP:3.84080
XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:6
Exact Mass:239.167399674
Heavy Atom Count:18
Complexity:202

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CC1=CC=CC=C1)NCCC2=CC=CC=C2

Technology Process of Benzeneethanamine, alpha-methyl-N-(2-phenylethyl)-

There total 7 articles about Benzeneethanamine, alpha-methyl-N-(2-phenylethyl)- 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: 94.0%

: 851219-33-5
N-(1-methyl-2-phenyl-ethyl)-2-nitro-N-phenethyl-benzenesulfonamide

: 21026-75-5,24997-89-5
N-Phenethyl-β-phenylisopropylamine

Guidance literature:: With potassium carbonate; thiophenol; In acetonitrile; at 50 ℃;
DOI:10.1039/b418168a

Reference yield: 55.0%

: 38084-50-3
Phenylacetic acid β-phenylisopropylamide

: 21026-75-5,24997-89-5
N-Phenethyl-β-phenylisopropylamine

Guidance literature:: With lithium aluminium tetrahydride; In benzene; Heating;
DOI:10.1007/BF00760702

Reference yield:

: 60-12-8
2-phenylethanol

: 21026-75-5,24997-89-5
N-Phenethyl-β-phenylisopropylamine

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / diphenyl-2-pyridylphosphine; di-tert-butyl azodicarboxylate / CH₂Cl₂ / 2 h / 20 °C

2: 40 percent / diphenyl-2-pyridylphosphine; di-tert-butyl azodicarboxylate / CH₂Cl₂ / 2 h / 20 °C

3: 94 percent / PhSH; potassium carbonate / acetonitrile / 50 °C

With 2-(diphenylphosphino)pyridine; di-tert-butyl-diazodicarboxylate; potassium carbonate; thiophenol; In dichloromethane; acetonitrile; 1: Mitsunobu reaction / 2: Mitsunobu reaction;
DOI:10.1039/b418168a