N-benzyl-2-(4-phenylmethoxyphenyl)ethanamine Hydrochloride

Base Information

Chemical Name:N-benzyl-2-(4-phenylmethoxyphenyl)ethanamine Hydrochloride
CAS No.:32293-43-9
Molecular Formula:C₂₂H₂₃NO*ClH
Molecular Weight:353.892
Hs Code.:
DSSTox Substance ID:DTXSID50468479
NSC Number:154576
Mol file:32293-43-9.mol

Synonyms:32293-43-9;N-benzyl-2-(4-phenylmethoxyphenyl)ethanamine Hydrochloride;SCHEMBL4456317;DTXSID50468479;NSC154576;NSC-154576;N-Benzyl-2-[4-(benzyloxy)phenyl]ethan-1-amine--hydrogen chloride (1/1)

Suppliers and Price of N-benzyl-2-(4-phenylmethoxyphenyl)ethanamine Hydrochloride

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

American Custom Chemicals Corporation
N-BENZYL-O-BENZYLTYRAMINE HYDROCHLORIDE 95.00%
5MG
$ 503.55

Total 8 raw suppliers

Chemical Property of N-benzyl-2-(4-phenylmethoxyphenyl)ethanamine Hydrochloride

Chemical Property:

Vapor Pressure:5.01E-09mmHg at 25°C
Boiling Point:470.6 °C at 760 mmHg
Flash Point:200.5 °C
PSA：21.26000
LogP:5.79080
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:8
Exact Mass:353.1546421
Heavy Atom Count:25
Complexity:312

Purity/Quality:

99% ^*data from raw suppliers

N-BENZYL-O-BENZYLTYRAMINE HYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNCCC2=CC=C(C=C2)OCC3=CC=CC=C3.Cl

Technology Process of N-benzyl-2-(4-phenylmethoxyphenyl)ethanamine Hydrochloride

There total 4 articles about N-benzyl-2-(4-phenylmethoxyphenyl)ethanamine Hydrochloride 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%

: 788824-90-8
N-t-butoxycarbonyl-N-benzyl-O-benzyltyramine

: 32293-43-9
N,O-dibenzyltyramine hydrochloride

Guidance literature:: With hydrogenchloride; In ethyl acetate; at 20 ℃;
DOI:10.1021/jm0505718

Reference yield:

: 182921-01-3
N-(tert-butoxycarbonyl)-2-[4-(benzyloxy)phenyl]ethylamine

: 32293-43-9
N,O-dibenzyltyramine hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaH / dimethylformamide / 0 °C

1.2: 80 percent / dimethylformamide / 2.75 h / 0 - 20 °C

2.1: 85 percent / HCl / ethyl acetate / 20 °C

With hydrogenchloride; sodium hydride; In ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm0505718

Reference yield:

: 51-67-2
tyrosamine

: 32293-43-9
N,O-dibenzyltyramine hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1.1: 91 percent / aq. NaHCO₃ / tetrahydrofuran / 24 h

2.1: 58 percent / K₂CO₃ / dimethylformamide / 20 °C

3.1: NaH / dimethylformamide / 0 °C

3.2: 80 percent / dimethylformamide / 2.75 h / 0 - 20 °C

4.1: 85 percent / HCl / ethyl acetate / 20 °C

With hydrogenchloride; sodium hydride; sodium hydrogencarbonate; potassium carbonate; In tetrahydrofuran; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm0505718