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CAS 270596-47-9

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Boc-(S)-3-amino-5-hexynoic acid

Description:
Boc-(S)-3-amino-5-hexynoic acid is a chemical compound characterized by its structure, which includes a protected amino group and a terminal alkyne. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, facilitating its use in peptide synthesis and other organic reactions without interfering with the amino group’s reactivity. The "S" designation indicates that the compound has a specific stereochemistry, which is crucial for biological activity and interactions. The presence of the hexynoic acid moiety contributes to its unique properties, including potential applications in medicinal chemistry and materials science. This compound is typically used in research settings, particularly in the synthesis of peptides or as an intermediate in the development of bioactive molecules. Its CAS number, 270596-47-9, allows for precise identification in chemical databases. Overall, Boc-(S)-3-amino-5-hexynoic acid is valued for its versatility in synthetic chemistry and its role in the development of complex organic structures.
Formula:C11H17NO4
InChI:InChI=1/C11H17NO4/c1-5-6-8(7-9(13)14)12-10(15)16-11(2,3)4/h1,8H,6-7H2,2-4H3,(H,12,15)(H,13,14)/t8-/m0/s1
SMILES:C#CC[C@@H](CC(=O)O)N=C(O)OC(C)(C)C
Synonyms:
  • (3S)-3-[(tert-butoxycarbonyl)amino]hex-5-ynoic acid
  • Boc-β-HoGly(Propargyl)-OH
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