Boc-3,5-Dibromo-L-tyrosine
95%
- Product Code: 122380
CAS:
58960-71-7
| Molecular Weight: | 439.11 g./mol | Molecular Formula: | C₁₄H₁₇Br₂NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00076993 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Boc-3,5-Dibromo-L-tyrosine is primarily used in peptide synthesis as a protected form of tyrosine. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, preventing unwanted reactions during the synthesis process. The dibromo modification on the aromatic ring of tyrosine allows for specific interactions or further functionalization in the synthesis of complex peptides or proteins. This compound is particularly valuable in the development of peptide-based drugs, where precise control over the structure and reactivity of amino acids is crucial. Additionally, it can be employed in biochemical research to study enzyme-substrate interactions or to create modified peptides with enhanced stability or activity. Its application extends to the field of medicinal chemistry, where it aids in the design of targeted therapeutics and the exploration of new bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿6,291.00 |
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| 5.000 | 10-20 days | ฿22,491.00 |
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Boc-3,5-Dibromo-L-tyrosine
Boc-3,5-Dibromo-L-tyrosine is primarily used in peptide synthesis as a protected form of tyrosine. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, preventing unwanted reactions during the synthesis process. The dibromo modification on the aromatic ring of tyrosine allows for specific interactions or further functionalization in the synthesis of complex peptides or proteins. This compound is particularly valuable in the development of peptide-based drugs, where precise control over the structure and reactivity of amino acids is crucial. Additionally, it can be employed in biochemical research to study enzyme-substrate interactions or to create modified peptides with enhanced stability or activity. Its application extends to the field of medicinal chemistry, where it aids in the design of targeted therapeutics and the exploration of new bioactive molecules.
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