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CAS 1609403-03-3

:

1-Piperidinecarboxylic acid, 4-amino-3-methyl-, 1,1-dimethylethyl ester, hydrochloride (1:1), (3R,4S)-rel-

Description:
1-Piperidinecarboxylic acid, 4-amino-3-methyl-, 1,1-dimethylethyl ester, hydrochloride (1:1), (3R,4S)-rel- is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. This compound features a carboxylic acid derivative with an ester functional group, indicating it is likely to exhibit moderate polarity and solubility in polar solvents. The presence of an amino group suggests potential basicity and reactivity, particularly in forming salts or participating in nucleophilic reactions. The specific stereochemistry denoted by (3R,4S) indicates the spatial arrangement of atoms around the chiral centers, which can significantly influence the compound's biological activity and interaction with receptors. As a hydrochloride salt, it is typically more stable and soluble in aqueous solutions, making it suitable for pharmaceutical applications. Overall, this compound's unique structural features contribute to its potential utility in medicinal chemistry and drug development.
Formula:C11H22N2O2·ClH
InChI:InChI=1/C11H22N2O2.ClH/c1-8-7-13(6-5-9(8)12)10(14)15-11(2,3)4;/h8-9H,5-7,12H2,1-4H3;1H/t8-,9+;/s2
InChI key:InChIKey=BJRKUDHNJGUHRE-LZPPVNAUNA-N
SMILES:C(OC(C)(C)C)(=O)N1C[C@H](C)[C@H](N)CC1.Cl
Synonyms:
  • 1-Piperidinecarboxylic acid, 4-amino-3-methyl-, 1,1-dimethylethyl ester, hydrochloride (1:1), (3R,4S)-rel-
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