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CAS 1097192-05-6

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Fmoc-(S)-2-amino-hept-6-ynoic acid

Description:
Fmoc-(S)-2-amino-hept-6-ynoic acid is a synthetic amino acid derivative commonly used in peptide synthesis and research. The "Fmoc" (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective reactions during peptide assembly. This compound features a unique alkyne functional group at the 6-position of the heptanoic acid chain, which can participate in various chemical reactions, including click chemistry, making it valuable for constructing complex molecular architectures. The (S) configuration indicates that it is a chiral molecule, which is significant in biological systems and can influence the activity and properties of peptides synthesized from it. The presence of the alkyne also allows for potential applications in bioconjugation and labeling studies. Overall, Fmoc-(S)-2-amino-hept-6-ynoic acid is a versatile building block in organic and medicinal chemistry, particularly in the development of peptide-based therapeutics.
Formula:C22H21NO4
Synonyms:
  • Fmoc-(S)-2-amino-hept-6-ynoic acid
  • ylmethoxy)carbonyl]amino]-, (2S)-
  • (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hept-6-ynoic acid
  • Fmoc-L-bishomopropargylglycine
  • 2S-{[(9H-fluorenyl-9-ylmethoxy)carbonyl]amino}-6-heptynoic acid
  • Fmoc-(S)-2-amino-hept-6-ynoic
  • (9H-Fluoren-9-yl)MethOxy]Carbonyl L-BisHomoPrapargylGly-OH
  • (S)-2-(((9H-FLUOREN-9-YL)METHOXY)CARBONYLAMINO)HEPT-6-YNOIC ACID
  • Fmoc-L-BisHomoPrapargylGly-OH
  • 6-Heptynoic acid, 2-[[(9H-fluoren-9-
  • Fmoc-L-BisHomoPrapargylGly-OH(Fmoc-(S)-2-amino-hept-6-ynoic acid)
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