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CAS 374794-75-9

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rel-1,1-Dimethylethyl (3R,4S)-3-hydroxy-4-methyl-1-piperidinecarboxylate

Description:
Rel-1,1-Dimethylethyl (3R,4S)-3-hydroxy-4-methyl-1-piperidinecarboxylate, with the CAS number 374794-75-9, is a chemical compound characterized by its piperidine structure, which includes a hydroxyl group and a carboxylate moiety. This compound is typically classified as an amino acid derivative due to the presence of the piperidine ring and the carboxylate functional group. The stereochemistry indicated by the (3R,4S) notation suggests specific spatial arrangements of the atoms, which can significantly influence the compound's biological activity and interactions. The presence of the dimethyl group contributes to its steric properties, potentially affecting its solubility and reactivity. Such compounds are often of interest in medicinal chemistry for their potential therapeutic applications, particularly in the development of pharmaceuticals. The specific configuration and functional groups can also play a crucial role in determining the compound's pharmacokinetics and pharmacodynamics. Overall, this compound exemplifies the complexity and diversity of organic molecules used in various chemical and biological contexts.
Formula:C11H21NO3
InChI:InChI=1/C11H21NO3/c1-8-5-6-12(7-9(8)13)10(14)15-11(2,3)4/h8-9,13H,5-7H2,1-4H3/t8-,9-/s2
InChI key:InChIKey=ADHBFIMXBSFQLJ-MDWBIBFBNA-N
SMILES:C(OC(C)(C)C)(=O)N1C[C@@H](O)[C@H](C)CC1
Synonyms:
  • rel-1,1-Dimethylethyl (3R,4S)-3-hydroxy-4-methyl-1-piperidinecarboxylate
  • (trans)-3-Hydroxy-4-methylpiperidine-1-carboxylic acid tert-butyl ester
  • 1-Piperidinecarboxylic acid, 3-hydroxy-4-methyl-, 1,1-dimethylethyl ester, (3R,4S)-rel-
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