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Home  > Fmoc-3,5-diiodo-l-tyrosine

AI05913

103213-31-6 | Fmoc-3,5-diiodo-l-tyrosine

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $27.00 $19.00 -   +
5g 95% in stock $82.00 $58.00 -   +
10g 95% in stock $153.00 $107.00 -   +
25g 95% in stock $358.00 $250.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AI05913
Chemical Name: Fmoc-3,5-diiodo-l-tyrosine
CAS Number: 103213-31-6
Molecular Formula: C24H19I2NO5
Molecular Weight: 655.2203
MDL Number: MFCD00063330
SMILES: O=C(N[C@H](C(=O)O)Cc1cc(I)c(c(c1)I)O)OCC1c2ccccc2c2c1cccc2

 

Upstream Synthesis Route
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3,5-diiodo-L-tyrosine is a versatile compound frequently utilized in chemical synthesis as a key intermediate for the modification and functionalization of various biomolecules. Its unique chemical structure, incorporating the fluorine and iodine substituents on the tyrosine residue, imparts distinct attributes that are crucial for designing novel compounds and materials in synthetic chemistry.In chemical synthesis, N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3,5-diiodo-L-tyrosine serves as a valuable building block for the creation of peptide conjugates, pharmaceuticals, and bioconjugates with enhanced properties. The presence of the fluorenylmethoxycarbonyl (Fmoc) protecting group enables selective deprotection under mild conditions, facilitating the sequential coupling of amino acids in peptide synthesis. Moreover, the strategic placement of diiodotyrosine provides a reactive site for cross-coupling reactions, facilitating the attachment of diverse functional groups or labels for molecular imaging or drug delivery purposes.Overall, the strategic incorporation of N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3,5-diiodo-L-tyrosine in chemical synthesis enhances the efficiency and versatility of organic reactions, opening up new avenues for the development of advanced materials, biologically active compounds, and molecular probes.
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