41820-21-7

Basic information

• Product Name: Phenethylamine, D-.alpha.-methyl-
• Synonyms: 1-Amphetamine hydrochloride;Nsc126789;(R)-Amphetamine Hydrochloride;(-)-PhenaMinuM Hydrochloride;(αR)-α-Methyl-benzeneethanaMine Hydrochloride;LevaMfetaMine Hydrochloride;l-α-MethylphenethylaMine Hydrochloride;(R)-AMphetaMine/(R)-1-phenylpropan-2-aMine
• CAS NO: 41820-21-7
• Molecular Formula: C₉H₁₃N*ClH
• Molecular Weight: 135.20622
• Product Categories: Amines;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 41820-21-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 152-154?C
• Appearance: /
• Storage Temp.: Hygroscopic, -20°C Freezer, Under Inert Atmosphere
• CAS DataBase Reference: Phenethylamine, D-.alpha.-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenethylamine, D-.alpha.-methyl-(41820-21-7)
• EPA Substance Registry System: Phenethylamine, D-.alpha.-methyl-(41820-21-7)

Safety Data

• Hazardous Substances Data: 41820-21-7(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Uses

CNS stimulant; anorexic. Controlled substance (stimulant).

Upstream product

• 154669-56-4 (2S)-2-[N-(tert-butoxycarbonyl)amino]-1-iodo-3-phenylpropane 
• 66605-57-0 (S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol 
• 3182-95-4 L-Phenylalaninol 
• 63-91-2 L-phenylalanine 
• 14593-16-9 N-acetylamphetamine 
• 167421-83-2 tert-butyl N-[(1R)-1-methyl-2-phenylethyl]carbamate 
• 75-16-1 methylmagnesium bromide 
• 221375-48-0 (N(E),R)-2-methyl-N-(2-phenylethylidene)-2-propanesulfinamide 
• 50505-64-1 (R,R)-(+)-N-(1-phenylethyl)-1-phenyl-2-aminopropane hydrochloride 

Downstream Products

• 132076-55-2 (R)-(-)-3-propiophenone hydrochloride 
• 1094619-98-3 (R)-6-(2-methoxyphenyl)-4-oxo-5-(1-phenylpropan-2-yl)-isothiazolo[5,4-d]pyrimidine-3-carboxamide 
• 1094619-97-2 (R)-methyl 6-(2-methoxyphenyl)-4-oxo-5-(1-phenylpropan-2-yl)-isothiazolo[5,4-d]pyrimidine-3-carboxylate 
• 1094619-52-9 (R)-6-(2-hydroxyphenyl)-4-oxo-5-(1-phenylpropan-2-yl)-isothiazolo[5,4-d]pyrimidine-3-carbonitrile 
• 1094619-99-4 (R)-6-(2-methoxyphenyl)-4-oxo-5-(1-phenylpropan-2-yl)-isothiazolo[5,4-d]pyrimidine-3-carbonitrile 
• 1094619-96-1 (R)-2-methoxy-N-(1-phenylpropan-2-yl)benzamide 
• 15547-41-8 (R)-3-methyl-3,4-dihydroisoquinoline 
• 1018678-55-1 (R)-4-amino-N-(1-phenylpropan-2-yl)-2-(trifluoromethyl)nicotinamide 
• 15302-18-8 (R)-N-(1-methyl-2-phenylethyl)formamide 

Relevant articles and documents

PHENETHYL SUBSTITUTED IMIDAZO[4,5-C]QUINOLINE COMPOUNDS WITH AN N-1 BRANCHED GROUP

Imidazo[4,5-c]quinoline compounds having a substituent that is attached at the N-1 position by a branched group, single enantiomers of the compounds, pharmaceutical compositions containing the compounds, and methods of making the compounds are disclosed.

Efficient procedure for the reduction of α-amino acids to enantiomerically pure α-methylamines

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Cytochrome P-455 nm Complex Formation in the Metabolism of Phenylalkylamines. 8. Stereoselectivity in Metabolic Intermediary Complex Formation with a Series of Chiral 2-Substituted 1-Phenyl-2-aminoethanes

The formation of cytochrome P-450 metabolic intermediary (MI) complexes from the enantiomers of four 2-alkyl-substituted 1-phenyl-2-aminoethanes was investigated during reduced nicotinamide adenine dinucleotide phosphate (NADPH) dependent metabolism in li