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CAS 1290191-65-9

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Phenylmethyl (2R,5S)-5-amino-2-methyl-1-piperidinecarboxylate

Description:
Phenylmethyl (2R,5S)-5-amino-2-methyl-1-piperidinecarboxylate is a chemical compound characterized by its piperidine structure, which includes a piperidine ring substituted with an amino group and a carboxylate moiety. The presence of the phenylmethyl group indicates that there is a phenyl ring attached to a methyl group, contributing to the compound's hydrophobic characteristics. The specific stereochemistry denoted by (2R,5S) suggests that the compound has chiral centers, which can influence its biological activity and interactions with other molecules. This compound may exhibit properties typical of piperidine derivatives, such as potential pharmacological effects, including analgesic or anti-inflammatory activities. Its solubility, stability, and reactivity can vary based on the functional groups present and the overall molecular structure. As with many organic compounds, the characteristics of this substance can be influenced by environmental factors such as pH and temperature, which may affect its behavior in biological systems or during chemical reactions.
Formula:C14H20N2O2
InChI:InChI=1S/C14H20N2O2/c1-11-7-8-13(15)9-16(11)14(17)18-10-12-5-3-2-4-6-12/h2-6,11,13H,7-10,15H2,1H3/t11-,13+/m1/s1
InChI key:InChIKey=MWKAMUJIXBCKIH-YPMHNXCESA-N
SMILES:C(OCC1=CC=CC=C1)(=O)N2[C@H](C)CC[C@H](N)C2
Synonyms:
  • 1-Piperidinecarboxylic acid, 5-amino-2-methyl-, phenylmethyl ester, (2R,5S)-
  • (-)-(2R,5S)-Benzyl 5-amino-2-methylpiperidine-1-carboxylate
  • Phenylmethyl (2R,5S)-5-amino-2-methyl-1-piperidinecarboxylate
  • benzyl (2R,5S)-5-amino-2-methylpiperidine-1-carboxylate
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