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63769-58-4

D-Tyrosine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-

Catalog#: AR00IBYT  |   CAS#: 63769-58-4  |   MDL#: MFCD00038249  |   MF: C21H25NO5  |   MW: 371.4269

Packsize Purity Price Availability Quantity
1g 97% $5.00 Global Stock Buy Now Add To Cart
5g 97% $17.00 Global Stock Buy Now Add To Cart
10g 97% $30.00 Global Stock Buy Now Add To Cart
25g 97% $65.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00IBYT
Chemical Name D-Tyrosine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-
CAS Number 63769-58-4
Molecular Formula C21H25NO5
Molecular Weight 371.4269
MDL Number MFCD00038249
SMILES OC(=O)[C@@H](Cc1ccc(cc1)OCc1ccccc1)NC(=O)OC(C)(C)C

Boc-D-Tyr(Bzl)-OH, also known as N-Boc-D-tyrosine benzyl ester, is a common building block used in peptide synthesis and organic chemistry. This compound serves as a protected form of D-tyrosine, where the amino group is temporarily blocked by the Boc (tert-butoxycarbonyl) group, and the carboxyl group is esterified with the benzyl group.In chemical synthesis, Boc-D-Tyr(Bzl)-OH plays a crucial role in the assembly of peptides and other complex organic molecules. By selectively protecting the amino group with the Boc group, chemists can control the order of chemical reactions and prevent side reactions from occurring. This protection strategy allows for the stepwise addition of amino acids in peptide synthesis, leading to the formation of desired peptide chains with high purity and yield.Moreover, the benzyl ester moiety on Boc-D-Tyr(Bzl)-OH can be cleaved under mild conditions using hydrogenation or acidic hydrolysis, enabling the deprotection of the tyrosine residue and the subsequent modification of the peptide chain. This flexibility in manipulation makes Boc-D-Tyr(Bzl)-OH a versatile tool for customizing and functionalizing peptides for various research and therapeutic applications.Overall, Boc-D-Tyr(Bzl)-OH is a valuable reagent in chemical synthesis, particularly in peptide chemistry, where precise control over amino acid manipulations is essential for the synthesis of bioactive peptides and peptide-based drugs.
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