(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(allyloxy)phenyl)propanoic acid

≥98%

  • Product Code: 38154
  CAS:    1175973-95-1
Molecular Weight: 443.49 g./mol Molecular Formula: C₂₇H₂₅NO₅
EC Number: MDL Number: MFCD08061623
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, store under inert gas
Product Description: This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amine functionality, enabling selective deprotection during solid-phase peptide synthesis. The allyloxy group on the phenyl ring can be utilized for further functionalization or as a protective group that can be removed under mild conditions. Its application is significant in the development of complex peptides and proteins, particularly in pharmaceutical research and bioconjugation studies. The compound’s structure allows for precise control over peptide assembly, making it valuable in the synthesis of bioactive peptides and peptidomimetics.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿1,530.00
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-
0.250 10-20 days ฿2,700.00
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(allyloxy)phenyl)propanoic acid
This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amine functionality, enabling selective deprotection during solid-phase peptide synthesis. The allyloxy group on the phenyl ring can be utilized for further functionalization or as a protective group that can be removed under mild conditions. Its application is significant in the development of complex peptides and proteins, particularly in pharmaceutical research and bioconjugation studies. The compound’s structure allows for precise control over peptide assembly, making it valuable in the synthesis of bioactive peptides and peptidomimetics.
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