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CAS 219297-13-9

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Boc-(S)-3-amino-4-(4-pyridyl)-butyric acid

Description:
Boc-(S)-3-amino-4-(4-pyridyl)-butyric acid is a chemical compound characterized by its structure, which includes a butyric acid backbone with an amino group and a pyridine ring. The "Boc" (tert-butyloxycarbonyl) group serves as a protecting group for the amino functionality, making it useful in peptide synthesis and other organic reactions. The presence of the (S) configuration indicates that the compound is a chiral molecule, which can exhibit specific biological activity or interact with biological systems in a particular manner. The 4-pyridyl group contributes to the compound's polarity and potential interactions with biological targets, making it of interest in medicinal chemistry. This compound is typically used in research and development, particularly in the synthesis of pharmaceuticals or as a building block in organic synthesis. Its solubility, stability, and reactivity can vary based on the conditions and solvents used, which are important considerations in its application in laboratory settings.
Formula:C14H20N2O4
InChI:InChI=1/C14H20N2O4/c1-14(2,3)20-13(19)16-11(9-12(17)18)8-10-4-6-15-7-5-10/h4-7,11H,8-9H2,1-3H3,(H,16,19)(H,17,18)/t11-/m0/s1
InChI key:BYTKQINZDKLYGV-NSHDSACASA-N
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccncc1)CC(=O)O)O
Synonyms:
  • (3S)-3-[(tert-butoxycarbonyl)amino]-4-pyridin-4-ylbutanoic acid
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