Boc-MeTyr-OH
97%
- Product Code: 55038
CAS:
82038-34-4
| Molecular Weight: | 295.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06658544 | |
| Melting Point: | Boiling Point: | 626.2°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is widely used in peptide synthesis as a protected form of tyrosine. It serves as a building block in the production of complex peptides, ensuring the tyrosine residue remains intact during the reaction process. The Boc (tert-butoxycarbonyl) group protects the amino group, while the methyl ester protects the carboxyl group, allowing selective deprotection and coupling in multi-step peptide synthesis. It is particularly valuable in pharmaceutical research for creating peptide-based drugs, where precise control over amino acid incorporation is essential. Additionally, it is employed in biochemical studies to investigate protein structure and function by incorporating modified tyrosine residues into peptides.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,978.00 |
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| 1.000 | 10-20 days | ฿10,026.00 |
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| 5.000 | 10-20 days | ฿30,213.00 |
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| 10.000 | 10-20 days | ฿47,241.00 |
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Boc-MeTyr-OH
This compound is widely used in peptide synthesis as a protected form of tyrosine. It serves as a building block in the production of complex peptides, ensuring the tyrosine residue remains intact during the reaction process. The Boc (tert-butoxycarbonyl) group protects the amino group, while the methyl ester protects the carboxyl group, allowing selective deprotection and coupling in multi-step peptide synthesis. It is particularly valuable in pharmaceutical research for creating peptide-based drugs, where precise control over amino acid incorporation is essential. Additionally, it is employed in biochemical studies to investigate protein structure and function by incorporating modified tyrosine residues into peptides.
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