114352-01-1

Basic information

• Product Name: (R)-amphetamine D-tartaric salt
• Synonyms: (R)-amphetamine D-tartaric salt
• CAS NO: 114352-01-1
• Molecular Weight: 285.297
• Mol File: 114352-01-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-amphetamine D-tartaric salt(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-amphetamine D-tartaric salt(114352-01-1)
• EPA Substance Registry System: (R)-amphetamine D-tartaric salt(114352-01-1)

Safety Data

• Hazardous Substances Data: 114352-01-1(Hazardous Substances Data)

Upstream product

• 147-71-7 D-tartaric acid 
• 60-15-1 2-amino-1-phenylpropane 
• 705-60-2 (2-nitroprop-1-enyl)benzene 
• 100-52-7 benzaldehyde 

Downstream Products

• 167421-83-2 tert-butyl N-[(1R)-1-methyl-2-phenylethyl]carbamate 
• 156-34-3 l-amphetamine 

Relevant articles and documents

Stereoisomers of Allenic Amines as Inactivators of Monoamine Oxidase Type B. Stereochemical Probes of the Active Site

The kinetics of inactivation of mitochondrial monoamine oxidase type B (MAO-B) by a series of 18 stereoisomers of tertiary α-allenic amines have been investigated in detail.The chirality of the allene group in N-methyl-N-aralkylpenta-2,3-dienamines was found to have a profound effect on the inactivation rate, with the (R)-allenes being up to 200-fold more potent than their (S)-allenic counterparts.The ability of (S)-allenes to inactivate MAO was severely compromised by the presence of N-phenethyl or N-α-substituted-aralkyl substituents.The opposing chiralities in both the allene and aralkyl groups of (R,R)- and (S,S)-N-methyl-N-(1,2,3,4-tetrahydro-1-naphthyl)-penta-2,3-dieneamine resulted in a difference of more than 3 oredrs of magnitude in inactivation rates.The stereoselectivity of MAO-B was examined further with a series of reversible aralkylamine inhibitors; thus (R)-1,2,3,4-tetrahydro-1-naphthylamine was determined to be 150-fold more potent than its enantiomer.