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CAS 175671-49-5

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2-Piperidinecarboxylicacid,4-hydroxy-,(2R,4S)-(9CI)

Description:
2-Piperidinecarboxylic acid, 4-hydroxy-, (2R,4S)-(9CI), also known as L-4-hydroxyproline, is an amino acid derivative characterized by its piperidine ring structure and a carboxylic acid functional group. This compound features a hydroxyl group at the fourth position of the piperidine ring, which contributes to its unique properties. It is a chiral molecule, existing in specific stereoisomeric forms, with the (2R,4S) configuration being biologically relevant. This compound is soluble in water and exhibits moderate stability under standard conditions. It is often utilized in biochemical research and pharmaceutical applications due to its role in protein synthesis and as a precursor for various bioactive compounds. Additionally, 2-Piperidinecarboxylic acid, 4-hydroxy-, has potential applications in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological and metabolic disorders. Its structural characteristics and functional groups make it a valuable compound in organic synthesis and medicinal chemistry.
Formula:C11H19NO5
InChI:InChI=1/C11H19NO5/c1-11(2,3)17-10(16)12-5-4-7(13)6-8(12)9(14)15/h7-8,13H,4-6H2,1-3H3,(H,14,15)/t7-,8+/m1/s1
Synonyms:
  • 1,2-piperidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-dimethylethyl) ester, (2S,4R)-
  • (2S,4R)-1-(tert-butoxycarbonyl)-4-hydroxypiperidine-2-carboxylic acid
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