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AE08373

112883-29-1 | Fmoc-d-tyr-oh

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $25.00 $17.00 -   +
5g 97% in stock $40.00 $28.00 -   +
10g 97% in stock $80.00 $56.00 -   +
25g 97% in stock $142.00 $99.00 -   +
100g 97% in stock $521.00 $365.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE08373
Chemical Name: Fmoc-d-tyr-oh
CAS Number: 112883-29-1
Molecular Formula: C24H21NO5
Molecular Weight: 403.4272
MDL Number: MFCD00171384
SMILES: O=C(N[C@@H](C(=O)O)Cc1ccc(cc1)O)OCC1c2ccccc2-c2c1cccc2

 

Upstream Synthesis Route
  • Fmoc-D-Tyr-OH, a derivative of the amino acid tyrosine, is a valuable reagent widely utilized in chemical synthesis for its unique properties. This compound is commonly employed in peptide synthesis, particularly in the formation of peptide bonds. Due to the presence of the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group, Fmoc-D-Tyr-OH serves as a versatile building block for constructing complex peptide structures.In solid-phase peptide synthesis, Fmoc-D-Tyr-OH plays a crucial role in the stepwise assembly of peptides on a solid support. The Fmoc protecting group shields the amine group of tyrosine, allowing for selective deprotection and subsequent coupling reactions with other amino acids. This enables efficient and controlled elongation of peptide chains with high purity and yield.Additionally, Fmoc-D-Tyr-OH can be utilized in the synthesis of peptide mimetics, modified peptides, and bioconjugates for various research and pharmaceutical applications. Its compatibility with standard peptide synthesis protocols and ease of manipulation make it a valuable tool in the chemical synthesis of diverse peptide compounds with tailored functionalities and properties.
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