Fmoc-Phe(4-CF3)-OH

≥95%

  • Product Code: 50395
  CAS:    247113-86-6
Molecular Weight: 455.43 g./mol Molecular Formula: C₂₅H₂₀F₃NO₄
EC Number: MDL Number: MFCD00797581
Melting Point: 128-138°C Boiling Point:
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. The presence of the trifluoromethyl (CF3) group on the phenyl ring enhances the hydrophobicity and stability of the peptide, making it useful in the development of peptides with specific structural or functional properties. It is often employed in the synthesis of modified peptides for research in drug discovery, biochemical studies, and the development of peptide-based therapeutics. The CF3 group can also influence the peptide's interaction with biological targets, making it valuable in designing peptides with enhanced binding affinity or selectivity.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days Ft7,854.32
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-
1.000 10-20 days Ft19,490.36
+
-
5.000 10-20 days Ft78,446.28
+
-
10.000 10-20 days Ft143,414.15
+
-
Fmoc-Phe(4-CF3)-OH
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. The presence of the trifluoromethyl (CF3) group on the phenyl ring enhances the hydrophobicity and stability of the peptide, making it useful in the development of peptides with specific structural or functional properties. It is often employed in the synthesis of modified peptides for research in drug discovery, biochemical studies, and the development of peptide-based therapeutics. The CF3 group can also influence the peptide's interaction with biological targets, making it valuable in designing peptides with enhanced binding affinity or selectivity.
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