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CAS 63039-48-5

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(S)-N-BOC-Propargylglycine

Description:
(S)-N-BOC-Propargylglycine is a chemical compound characterized by its unique structure, which includes a propargyl group and a protected amino acid functionality. The "N-BOC" designation indicates that the amine group is protected by a tert-butyloxycarbonyl (BOC) group, which is commonly used in organic synthesis to temporarily mask the reactivity of amines. This compound is typically utilized in peptide synthesis and medicinal chemistry due to its ability to introduce alkyne functionalities, which can participate in various coupling reactions, including click chemistry. The presence of the propargyl group allows for further functionalization, making it a versatile building block in the development of bioactive molecules. Additionally, (S)-N-BOC-Propargylglycine is often studied for its potential applications in drug design and development, particularly in the context of targeting specific biological pathways. Its chirality, indicated by the (S) configuration, is crucial for its biological activity, as enantiomers can exhibit significantly different properties in biological systems.
Formula:C10H14NO4
InChI:InChI=1/C10H15NO4/c1-5-6-7(8(12)13)11-9(14)15-10(2,3)4/h1,7H,6H2,2-4H3,(H,11,14)(H,12,13)/p-1/t7-/m0/s1
SMILES:C#CC[C@@H](C(=O)[O-])N=C(O)OC(C)(C)C
Synonyms:
  • (S)-N-tert-Butoxycarbonyl-2-amino-4-pentynoic acid
  • Boc-L-Propargylglycine
  • (2S)-2-[(tert-butoxycarbonyl)amino]pent-4-ynoic acid
  • (2S)-2-[(tert-butoxycarbonyl)amino]pent-4-ynoate
  • Boc-(S)-2-Propargylglycine
  • Boc-Pra-OH
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