L-TYROSINE, N[(1,1-DIMETHYLETHOXY) CARBONYL] -2,6
98%
- Product Code: 38155
CAS:
99953-00-1
| Molecular Weight: | 309.36 g./mol | Molecular Formula: | C₁₆H₂₃NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 174-177 °C | Boiling Point: | 512.0±50.0 °C(Predicted) |
| Density: | 1.191±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃, dry |
Product Description:
This compound is primarily utilized in peptide synthesis as a protecting group for the amino acid tyrosine. The tert-butoxycarbonyl (Boc) group shields the amino functionality during the synthesis process, preventing unwanted side reactions. This protection is crucial in multi-step peptide synthesis, where selective deprotection allows for the sequential addition of amino acids. It is particularly valuable in the production of complex peptides and proteins for research, pharmaceutical development, and biochemical studies. Additionally, its stability under various reaction conditions makes it a reliable choice in organic synthesis and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $823.58 |
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L-TYROSINE, N[(1,1-DIMETHYLETHOXY) CARBONYL] -2,6
This compound is primarily utilized in peptide synthesis as a protecting group for the amino acid tyrosine. The tert-butoxycarbonyl (Boc) group shields the amino functionality during the synthesis process, preventing unwanted side reactions. This protection is crucial in multi-step peptide synthesis, where selective deprotection allows for the sequential addition of amino acids. It is particularly valuable in the production of complex peptides and proteins for research, pharmaceutical development, and biochemical studies. Additionally, its stability under various reaction conditions makes it a reliable choice in organic synthesis and medicinal chemistry.
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