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CAS 1268520-05-3

:

rel-Phenylmethyl (3R,4R)-4-amino-3-fluoro-1-piperidinecarboxylate

Description:
Rel-Phenylmethyl (3R,4R)-4-amino-3-fluoro-1-piperidinecarboxylate is a chemical compound characterized by its piperidine core, which features a fluorine atom and an amino group at specific positions on the ring. The presence of the phenylmethyl group contributes to its lipophilicity, potentially influencing its biological activity and interaction with various receptors. The stereochemistry indicated by the (3R,4R) configuration suggests specific spatial arrangements of the substituents, which can significantly affect the compound's pharmacological properties. This compound may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals targeting neurological or psychiatric conditions. Its unique structure may also allow for specific interactions with biological targets, making it a candidate for further research in drug development. As with many compounds in this class, understanding its solubility, stability, and reactivity is crucial for assessing its potential applications in therapeutic contexts.
Formula:C13H17FN2O2
InChI:InChI=1/C13H17FN2O2/c14-11-8-16(7-6-12(11)15)13(17)18-9-10-4-2-1-3-5-10/h1-5,11-12H,6-9,15H2/t11-,12-/s2
InChI key:InChIKey=SYVUWEZGXXHYPH-XXCBQWOANA-N
SMILES:C(OCC1=CC=CC=C1)(=O)N2C[C@@H](F)[C@H](N)CC2
Synonyms:
  • 1-Piperidinecarboxylic acid, 4-amino-3-fluoro-, phenylmethyl ester, (3R,4R)-rel-
  • rel-Phenylmethyl (3R,4R)-4-amino-3-fluoro-1-piperidinecarboxylate
  • (3R,4R)-rel-Benzyl 4-amino-3-fluoropiperidine-1-carboxylate
  • trans-1-Cbz-4-aMino-3-fluoropiperidine
  • benzyl trans-4-amino-3-fluoropiperidine-1-carboxylate
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