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CAS 1161932-04-2

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(3S,4S)-4-aMino-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester

Description:
(3S,4S)-4-Amino-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester is a chemical compound characterized by its piperidine ring structure, which features a hydroxyl group and an amino group at specific positions. This compound is a derivative of piperidine, a six-membered nitrogen-containing heterocycle, and is notable for its chirality, as indicated by the (3S,4S) configuration. The tert-butyl ester group enhances its lipophilicity, potentially influencing its solubility and bioavailability in various applications, particularly in medicinal chemistry. The presence of both amino and hydroxyl functional groups suggests that this compound may participate in hydrogen bonding, which can affect its reactivity and interactions with biological targets. Additionally, the compound may serve as a building block in the synthesis of more complex molecules, especially in the development of pharmaceuticals. Its specific properties, such as melting point, boiling point, and reactivity, would depend on the conditions under which it is studied or utilized.
Formula:C10H20N2O3
InChI:InChI=1S/C10H20N2O3/c1-10(2,3)15-9(14)12-5-4-7(11)8(13)6-12/h7-8,13H,4-6,11H2,1-3H3/t7-,8-/m0/s1
InChI key:KREUZCYJWPQPJX-YUMQZZPRSA-N
SMILES:CC(C)(C)OC(=O)N1CC[C@@H]([C@H](C1)O)N
Synonyms:
  • (3S,4S)-4-Amino-1-Boc-piperidin-3-ol
  • 1-Piperidinecarboxylic acid, 4-amino-3-hydroxy-, 1,1-dimethylethyl ester, (3S,4S)-
  • (3S,4S)-1-Boc-4-amino-3-hydroxy-piperidine
  • CPD3642
  • (3S,4S)-4-aMino-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester
  • (3S,4S)-tert-Butyl 4-amino-3-hydroxypiperidine-1-carboxylate
  • tert-butyl (3S,4S)-4-amino-3-hydroxypiperidine-1-carboxylate
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