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CAS 1434073-26-3

:

rel-1,1-Dimethylethyl (2R,4S)-4-amino-2-methyl-1-piperidinecarboxylate

Description:
Rel-1,1-Dimethylethyl (2R,4S)-4-amino-2-methyl-1-piperidinecarboxylate is a chemical compound characterized by its piperidine structure, which includes a piperidine ring with an amino group and a carboxylate functional group. The presence of the dimethyl group contributes to its steric properties, influencing its reactivity and interaction with biological targets. The specific stereochemistry indicated by the (2R,4S) configuration suggests that the compound exhibits chirality, which can significantly affect its pharmacological activity and interactions in biological systems. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential biological activity. Its solubility, stability, and reactivity can vary based on the functional groups present and the overall molecular structure. As with many piperidine derivatives, it may exhibit properties such as being a potential ligand for receptors or enzymes, making it a candidate for further research in drug development and therapeutic applications.
Formula:C11H22N2O2
InChI:InChI=1/C11H22N2O2/c1-8-7-9(12)5-6-13(8)10(14)15-11(2,3)4/h8-9H,5-7,12H2,1-4H3/t8-,9+/s2
InChI key:InChIKey=OGIPSHDJYIEDKG-BRJQIKQINA-N
SMILES:C(OC(C)(C)C)(=O)N1[C@H](C)C[C@@H](N)CC1
Synonyms:
  • 1-Piperidinecarboxylic acid, 4-amino-2-methyl-, 1,1-dimethylethyl ester, (2R,4S)-rel-
  • rel-1,1-Dimethylethyl (2R,4S)-4-amino-2-methyl-1-piperidinecarboxylate
  • trans-tert-Butyl 4-amino-2-methylpiperidine-1-carboxylate
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