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CAS 169209-63-6

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(2R,4R)-APDC

Description:
(2R,4R)-APDC, or (2R,4R)-2-amino-4-phenyl-1,3-thiazolidine-4-carboxylic acid, is a chiral compound characterized by its specific stereochemistry, which is crucial for its biological activity. This substance typically appears as a white to off-white solid and is soluble in polar solvents, reflecting its functional groups. The presence of both amino and carboxylic acid groups contributes to its potential as a ligand in coordination chemistry and its utility in pharmaceutical applications. Its thiazolidine ring structure imparts unique reactivity, making it a candidate for various synthetic transformations. The compound's chirality is significant in the context of drug design, as enantiomers can exhibit different biological effects. Additionally, (2R,4R)-APDC may participate in hydrogen bonding due to its functional groups, influencing its interactions in biological systems. Overall, its structural features and stereochemistry make it a compound of interest in both organic synthesis and medicinal chemistry.
Formula:C6H10N2O4
InChI:InChI=1S/C6H10N2O4/c7-6(5(11)12)1-3(4(9)10)8-2-6/h3,8H,1-2,7H2,(H,9,10)(H,11,12)/t3-,6-/m1/s1
InChI key:XZFMJVJDSYRWDQ-AWFVSMACSA-N
SMILES:C1[C@@H](NC[C@]1(C(=O)O)N)C(=O)O
Synonyms:
  • Ly-314,593
  • (2R,4R)-4-Aminopyrrolidine-2,4-Dicarboxylate
  • (2R,4R)-4-Aminopyrrolidine-2,4-Dicarboxylic Acid
  • 2,4-Pyrrolidinedicarboxylicacid,4-amino-,(2R,4R)-(9CI)
  • 2,4-Pyrrolidinedicarboxylic acid, 4-amino-, (2R,4R)-
  • (2R,4R)-APDC
  • 4-amino-2,4-pyrrolidinedicarboxylic acid
  • 2R, 4R-APDC monohydrate
Found 4 products.