[2-(Phenylthio)ethyl]amine hydrochloride

Base Information

Chemical Name:[2-(Phenylthio)ethyl]amine hydrochloride
CAS No.:34946-13-9
Molecular Formula:C8H12ClNS
Molecular Weight:189.709
Hs Code.:
DSSTox Substance ID:DTXSID40956411
Mol file:34946-13-9.mol

Synonyms:34946-13-9;[2-(phenylthio)ethyl]amine hydrochloride;MFCD00464838;2-(Phenylthio)ethan-1-amine hydrochloride;2-phenylsulfanylethanamine;hydrochloride;SCHEMBL3671919;[2-(Phenylthio)ethyl]amine HCl;DTXSID40956411;2-(Phenylthio)ethanaminehydrochloride;AKOS016367766;BS-40720;CS-0320281;2-(phenylsulfanyl)ethan-1-amine hydrochloride;2-(PHENYLSULFANYL)ETHANAMINE HYDROCHLORIDE;2-(Phenylsulfanyl)ethan-1-amine--hydrogen chloride (1/1)

Suppliers and Price of [2-(Phenylthio)ethyl]amine 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

TRC
[2-(phenylthio)ethyl]aminehydrochloride
50mg
$ 45.00

ChemBridge Corporation
[2-(phenylthio)ethyl]aminehydrochloride 95%
250 mg
$ 64.00

Total 5 raw suppliers

Chemical Property of [2-(Phenylthio)ethyl]amine hydrochloride

Chemical Property:

Vapor Pressure:0.0191mmHg at 25°C
Melting Point:160-161 °C
Boiling Point:252.6°Cat760mmHg
Flash Point:106.6°C
PSA：51.32000
Density:g/cm³
LogP:3.23970
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:189.0378983
Heavy Atom Count:11
Complexity:79.3

Purity/Quality:

99% ^*data from raw suppliers

[2-(phenylthio)ethyl]aminehydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)SCCN.Cl

Technology Process of [2-(Phenylthio)ethyl]amine hydrochloride

There total 3 articles about [2-(Phenylthio)ethyl]amine 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: 99.0%

: 106118-84-7
(2-azidoethyl)(phenyl)sulfane

: 34946-13-9
(2-aminoethyl) phenyl sulfide hydrochloride

Guidance literature:: (2-azidoethyl)(phenyl)sulfane; With 1,3-diphenyl-disiloxane; triphenylphosphine; at 20 ℃; for 24h;

With water;

With hydrogenchloride; In 1,4-dioxane; chemoselective reaction;
DOI:10.1021/acs.joc.9b00831

Reference yield: 85.0%

: 141858-26-6
(2-Phenylsulfanyl-ethyl)-phosphoramidic acid dimethyl ester

: 34946-13-9
(2-aminoethyl) phenyl sulfide hydrochloride

Guidance literature:: With hydrogenchloride; In toluene; for 48h; Ambient temperature;

Reference yield:

: 4837-01-8
1-bromo-2-phenylthioethane

: 34946-13-9
(2-aminoethyl) phenyl sulfide hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium azide / acetone; water / 23 °C

2.1: triphenylphosphine / 20 h / 110 °C / Green chemistry

2.2: Green chemistry

With sodium azide; triphenylphosphine; In water; acetone; 2.1: |Staudinger Azide Reduction;
DOI:10.1039/c8gc02136h