Fmoc-3,5-dibromo-Tyr-OH, also known as Fmoc-3,5-dibromo-tyrosine, is a derivative of the amino acid tyrosine, characterized by the presence of two bromine atoms at the 3 and 5 positions of the aromatic ring. The "Fmoc" (9-fluorenylmethoxycarbonyl) group is a common protecting group used in peptide synthesis, which helps to prevent unwanted reactions during the coupling process. This compound is typically utilized in the field of organic chemistry and peptide synthesis, particularly in the development of modified peptides for research and therapeutic applications. The presence of bromine atoms can enhance the compound's reactivity and influence its biological properties. Fmoc-3,5-dibromo-Tyr-OH is soluble in organic solvents and exhibits stability under standard laboratory conditions. Its unique structure allows for specific interactions in biological systems, making it a valuable tool in the study of protein function and structure. As with all chemical substances, proper handling and safety precautions should be observed when working with this compound.

Fmoc-3,5-dibromo-Tyr-OH

Fmoc-3,5-dibromo-L-tyrosine

L-Tyrosine, 3,5-dibromo-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-

This is a synthetic compound that is used as a reagent in organic chemistry. Fmoc-3,5-dibromo-L-tyrosine is a white solid that is soluble in water and methanol. It has been used to synthesize peptides and proteins.

CAS 201484-26-6: Fmoc-3,5-dibromo-Tyr-OH

Fmoc-3,5-dibromo-L-tyrosine

Ref: 7W-GM2797

L-Tyrosine, 3,5-dibromo-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-

Ref: IN-DA002DFU

Fmoc-3,5-dibromo-L-tyrosine

Ref: 3D-FF47875

(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(3,5-dibromo-4-hydroxyphenyl)propanoic acid

Ref: 10-F771802

Fmoc-3,5-dibromo-Tyr-OH

Ref: 01-4008952