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CAS 152491-46-8

:

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

Description:
Rel-1,1-Dimethylethyl (2R,4S)-4-hydroxy-2-methyl-1-piperidinecarboxylate, with CAS number 152491-46-8, is a chemical compound characterized by its piperidine structure, which includes a hydroxyl group and a carboxylate moiety. This compound is notable for its chirality, possessing specific stereochemistry at the 2 and 4 positions of the piperidine ring, which can influence its biological activity and interactions. The presence of the dimethyl group contributes to its steric properties, potentially affecting its solubility and reactivity. Typically, compounds of this nature may exhibit pharmacological properties, making them of interest in medicinal chemistry. The hydroxyl group can participate in hydrogen bonding, enhancing solubility in polar solvents, while the carboxylate can engage in ionic interactions. Overall, the unique structural features of this compound suggest potential applications in drug development and synthesis, although specific biological activities would require further investigation through experimental studies.
Formula:C11H21NO3
InChI:InChI=1/C11H21NO3/c1-8-7-9(13)5-6-12(8)10(14)15-11(2,3)4/h8-9,13H,5-7H2,1-4H3/t8-,9+/s2
InChI key:InChIKey=RCXJVQLRZJXWNM-BRJQIKQINA-N
SMILES:C(OC(C)(C)C)(=O)N1[C@H](C)C[C@@H](O)CC1
Synonyms:
  • trans-4-Hydroxy-2-methylpiperidine-1-carboxylic acid tert-butyl ester
  • 1-Piperidinecarboxylic acid, 4-hydroxy-2-methyl-, 1,1-dimethylethyl ester, (2R,4S)-rel-
  • rel-1,1-Dimethylethyl (2R,4S)-4-hydroxy-2-methyl-1-piperidinecarboxylate
  • 1-Piperidinecarboxylic acid, 4-hydroxy-2-methyl-, 1,1-dimethylethyl ester, trans-
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