Selegiline

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Identification

Molecular formula
C13H17N
CAS Number
14611-51-9
IUPAC Name
(2R)-N-methyl-1-phenyl-N-prop-2-ynyl-propan-2-amine
Molecular Weight
187.30g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0000g/cm3
Synonyms
selegiline
Interesting facts

Interesting Facts about (2R)-N-methyl-1-phenyl-N-prop-2-ynyl-propan-2-amine

(2R)-N-methyl-1-phenyl-N-prop-2-ynyl-propan-2-amine is a fascinating compound known for its unique properties and applications in various fields. Here are some noteworthy points about this compound:

  • Synthetic Utility: This compound serves as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows chemists to modify and synthesize a variety of derivatives.
  • Chirality: The designation of the (2R) configuration highlights its chiral nature, which plays a crucial role in biological activity. Chiral compounds can exhibit different actions in biological systems, making their study critical in medicinal chemistry.
  • Medical Significance: Compounds similar to (2R)-N-methyl-1-phenyl-N-prop-2-ynyl-propan-2-amine have shown potential in the treatment of neurological disorders, particularly as stimulants or antidepressants. This opens pathways for further research into their pharmacological effects.
  • Binding Affinity: As with many amine-based compounds, variations in structure can lead to significant changes in binding affinity to neurotransmitter receptors, which is key for their effectiveness in therapeutic applications.
  • Research Applications: The compound is often used in research settings to probe mechanisms of action in neurochemistry and psychopharmacology. Scientists aim to unveil how modifications can enhance or alter activity.

In summary, (2R)-N-methyl-1-phenyl-N-prop-2-ynyl-propan-2-amine is not just a chemical compound; it embodies the intersection of synthesis, pharmacology, and neuroscience. Its chiral nature and synthetic versatility make it a compound of significant interest in contemporary research.

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