(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5,5,5-trifluoropentanoic acid

98%

  • Product Code: 104341
  CAS:    144207-41-0
Molecular Weight: 393.36 g./mol Molecular Formula: C₂₀H₁₈F₃NO₄
EC Number: MDL Number: MFCD31580021
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS) methods. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactions during the peptide chain assembly. The trifluoropentanoic acid moiety can introduce specific properties into the peptide, such as enhanced stability or unique interactions in biological systems. It is particularly valuable in the development of peptides for pharmaceutical research, where precise control over structure and function is critical. Additionally, its application extends to the study of protein-protein interactions and the design of peptide-based therapeutics.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $515.66
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0.250 10-20 days $772.65
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1.000 10-20 days $1,932.47
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5,5,5-trifluoropentanoic acid
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS) methods. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactions during the peptide chain assembly. The trifluoropentanoic acid moiety can introduce specific properties into the peptide, such as enhanced stability or unique interactions in biological systems. It is particularly valuable in the development of peptides for pharmaceutical research, where precise control over structure and function is critical. Additionally, its application extends to the study of protein-protein interactions and the design of peptide-based therapeutics.
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