Fmoc-L-3-iodophenylalanine is a modified amino acid commonly used in peptide synthesis and research. It features a phenylalanine backbone with an iodine atom substituted at the meta position of the aromatic ring, which can influence the compound's reactivity and properties. The Fmoc (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective deprotection during peptide synthesis. This compound is typically utilized in solid-phase peptide synthesis due to its stability and ease of handling. Its unique characteristics, such as the presence of the iodine atom, can enhance the biological activity of peptides, making it valuable in medicinal chemistry and drug development. Additionally, the Fmoc group facilitates purification and characterization of peptides. Overall, Fmoc-L-3-iodophenylalanine is a versatile building block in the field of peptide chemistry, contributing to the synthesis of complex biomolecules with potential therapeutic applications.

fmoc-l-3-iodophenylalanine

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L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-iodo-

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

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CAS 210282-31-8: fmoc-l-3-iodophenylalanine

L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-iodo-

Ref: IN-DA002KNT

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

Ref: 10-F611954

Fmoc-3-iodo-L-phenylalanine

Ref: 3D-FF50057

Fmoc-3-iodo-L-phenylalanine

Ref: 54-BIF0125