CAS 1085-42-3

Benzylamphetamine

Description:

Benzylamphetamine, with the CAS number 1085-42-3, is a chemical compound that belongs to the class of substituted amphetamines. It is characterized by the presence of a benzyl group attached to the nitrogen atom of the amphetamine structure, which contributes to its unique properties. This compound typically exhibits stimulant effects on the central nervous system, similar to other amphetamines, and may influence neurotransmitter activity, particularly dopamine and norepinephrine. Benzylamphetamine is often studied for its potential applications in pharmacology and neuroscience, although its use may be restricted or regulated in various jurisdictions due to its structural similarity to controlled substances. In terms of physical properties, it is generally a solid at room temperature, with solubility in organic solvents. Safety and handling precautions are essential when working with this compound, as it may pose health risks if ingested or improperly handled. As with many amphetamines, research into its effects and potential therapeutic uses continues to evolve.

Formula: C₁₆H₁₉N

InChI: InChI=1S/C16H19N/c1-14(12-15-8-4-2-5-9-15)17-13-16-10-6-3-7-11-16/h2-11,14,17H,12-13H2,1H3

InChI key: InChIKey=JLCDKDGHTWGGQM-UHFFFAOYSA-N

SMILES: C(C(NCC1=CC=CC=C1)C)C2=CC=CC=C2

Synonyms:

• 1-Phenyl-2-(benzylamino)propane
• 1-Phenyl-2-[(phenylmethyl)amino]propane
• 1-Phenyl-2-benzylamino-propan
• 1-Phenyl-2-benzylamino-propan [German]
• 1-Phenyl-2-benzylaminopropane
• Benzeneethanamine, α-methyl-N-(phenylmethyl)-
• Benzylamphetamine
• N-Benzyl-α-methylphenethylamine
• N-Benzylamphetamine
• N-benzyl-1-phenylpropan-2-amine
• Phenethylamine, N-benzyl-alpha-methyl-
• Phenethylamine, N-benzyl-α-methyl-
• α-Methyl-N-(phenylmethyl)benzeneethanamine

Benzyl(1-phenylpropan-2-yl)amine

Controlled Product

CAS: 1085-42-3

Benzyl(1-phenylpropan-2-yl)amine is a piperidine derivative that acts as an inhibitor of cytochrome P450 enzymes. It binds to the CYP2D6 enzyme and has been shown to have an inhibitory effect on the activity of this enzyme in rat liver microsomes. The binding constants for benzyl(1-phenylpropan-2-yl)amine with the CYP2D6 enzyme were determined by competitive inhibition studies and it was found that this compound has a high binding affinity with the CYP2D6 enzyme. Studies also demonstrated that benzyl(1-phenylpropan-2-yl)amine inhibits the activity of CYP3A4 and CYP3A5 enzymes. This drug may be useful in treating some individuals who are taking drugs metabolized by these two enzymes, but will not be effective in people who are not taking any drugs metabolized by these two enzymes.

Formula: C₁₆H₁₉N

Purity: Min. 95%

Molecular weight: 225.33 g/mol

Ref: 3D-BAA08542