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CAS 136329-39-0

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(αR)-N-Methyl-α-phenyl-1-pyrrolidineethanamine

Description:
(αR)-N-Methyl-α-phenyl-1-pyrrolidineethanamine, also known as a specific enantiomer of a substituted phenylpyrrolidine, is a chemical compound characterized by its chiral structure, which influences its pharmacological properties. This compound features a pyrrolidine ring, a methyl group, and a phenyl group, contributing to its potential activity as a psychoactive substance. It is typically classified within the category of amphetamines due to its structural similarities and may exhibit stimulant effects. The presence of the methyl group on the nitrogen atom enhances its lipophilicity, potentially affecting its ability to cross the blood-brain barrier. The specific stereochemistry (αR) is crucial, as it can significantly alter the compound's interaction with biological targets, including neurotransmitter receptors. As with many compounds in this class, its safety profile, therapeutic applications, and regulatory status are essential considerations in research and development contexts. Overall, this compound exemplifies the importance of stereochemistry in determining the biological activity of chemical substances.
Formula:C13H20N2
InChI:InChI=1S/C13H20N2/c1-14-13(11-15-9-5-6-10-15)12-7-3-2-4-8-12/h2-4,7-8,13-14H,5-6,9-11H2,1H3/t13-/m0/s1
InChI key:InChIKey=ZINZYRWMDNKTBY-ZDUSSCGKSA-N
SMILES:[C@@H](CN1CCCC1)(NC)C2=CC=CC=C2
Synonyms:
  • (R)-N-Methyl-1-phenyl-2-(1-pyrrolidinyl)ethanamine
  • (R)-N-Methyl-1-phenyl-2-(pyrrolidin-1-yl)ethanamine
  • (αR)-N-Methyl-α-phenyl-1-pyrrolidineethanamine
  • 1-Pyrrolidineethanamine N-methyl-α-phenyl-, (αR)-
  • 1-Pyrrolidineethanamine, N-methyl-α-phenyl-, (R)-
  • Asimadilin
  • Asimadiline
  • N-methyl-1-phenyl-2-pyrrolidin-1-ylethanamine
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