(+)-N-(o-chlorobenzyl)-alpha-methylphenethylamine hydrochloride

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Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: Product Name:BA-7205
CAS:5843-53-8
Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G
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Products Intro: Product Name:(+)-N-(o-chlorobenzyl)-alpha-methylphenethylamine hydrochloride
CAS:5843-53-8
Purity:0.99
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Products Intro: Product Name:Clobenzorex Hydrochloride
CAS:5843-53-8
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Products Intro: Product Name:BenzeneethanaMine,N-[(2-chlorophenyl)Methyl]-a-Methyl-, hydrochloride (1:1), (+)-
CAS:5843-53-8
Purity:99.70% Package:Pints
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Products Intro: Product Name:ClobenzorexHCl
CAS:5843-53-8
Purity:98% HPLC Package:1G;5G
(+)-N-(o-chlorobenzyl)-alpha-methylphenethylamine hydrochloride Basic information
Product Name:(+)-N-(o-chlorobenzyl)-alpha-methylphenethylamine hydrochloride
Synonyms:BenzeneethanaMine,N-[(2-chlorophenyl)Methyl]-a-Methyl-, hydrochloride (1:1), (+)-;(2-chlorobenzyl)-(1-methyl-2-phenyl-ethyl)amine hydrochloride;N-(2-chlorobenzyl)-1-phenylpropan-2-amine hydrochloride;BA-7205;Chlorhydrate de D-N-(phenyl-1 propyl-2) chloro-2 benzylamine;Chlorhydrate de D-N-(phenyl-1 propyl-2) chloro-2 benzylamine [french];Einecs 227-434-5;(S)-(+)-Clobenzorex Hydrochloride
CAS:5843-53-8
MF:C16H19Cl2N
MW:296.23476
EINECS:227-434-5
Product Categories:Amines;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:5843-53-8.mol
(+)-N-(o-chlorobenzyl)-alpha-methylphenethylamine hydrochloride Structure
(+)-N-(o-chlorobenzyl)-alpha-methylphenethylamine hydrochloride Chemical Properties
Melting point 182-183° (isopropanol)
alpha D20 +26.3° (water)
solubility Methanol (Slightly), Water (Slightly, Heated)
form Solid
color White to Off-White
Safety Information
ToxicityLD50 i.p. in mice: 103 mg/kg (Boissier et al.)
MSDS Information
(+)-N-(o-chlorobenzyl)-alpha-methylphenethylamine hydrochloride Usage And Synthesis
Chemical PropertiesWhite Solid
OriginatorAsenlix,Aventis
UsesThe S-enantiomer of Clobenzorex (C583000), an anorexic.
Manufacturing ProcessA solution of 21.0 g (0.15 mol) of 2-chlorobenzaldehyde in 100 ml of ethanol (95%) was added to a solution of 20.5 g (0.152 mol) of D-1-phenyl-2-aminopropane in 100 ml of ethanol (95%). After standing for 15 h at room temperature, the ethanol was driven off, and the oily residue was then distilled to yield 36.2 g (94%) of D-N-(2-chlorobenzylidene)-2-amino-1- phenylpropane, boiling point 142°-146°C/0.1 mm Hg.
To the solution of 36.0 g (0.14 mol) of D-N-(2-chlorobenzylidene)-2-amino-1- phenylpropane in 200 ml of dry methanol were added, in portions, 5.3 g (0.14 mol) of sodium borohydride. The mixture was stirred for 1 h at room
temperature, and refluxed for 1 h water (100 ml) was then added and the methanol was removed in vacuo. After acidifying carefully with dilute hydrochloric acid, the solution was made alkaline by dilute sodium hydroxide, and extracted with ether. 33.0 g (90%) of D-N-(1-phenyl-2-propyl)-2-
chlorobenzylamine, boiling point 132°-134°C/0.1 mm Hg, were obtained by distillation.
Therapeutic FunctionAnorexic
(+)-N-(o-chlorobenzyl)-alpha-methylphenethylamine hydrochloride Preparation Products And Raw materials
Raw materialsD-AMPHETAMINE HYDROCHLORIDE-->Sodium hydroxide-->2-Chlorobenzaldehyde
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