N-(tert-Butoxycarbonyl)-L-tyrosine Benzyl Ester
≥98%
- Product Code: 57994
CAS:
19391-35-6
| Molecular Weight: | 371.43 g./mol | Molecular Formula: | C₂₁H₂₅NO₅ |
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| EC Number: | MDL Number: | MFCD00190840 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is widely used in peptide synthesis as a protecting group for tyrosine. The tert-butoxycarbonyl (Boc) group safeguards the amino functionality, while the benzyl ester protects the carboxyl group during the synthesis process. It is particularly valuable in solid-phase peptide synthesis (SPPS) where selective deprotection is required to build complex peptides step-by-step. The Boc group can be removed under acidic conditions without affecting the benzyl ester, allowing for precise control over the synthesis. This makes it a crucial reagent in the production of peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and ease of removal under mild conditions make it a preferred choice for protecting tyrosine residues in peptide chains.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $83.27 |
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| 1.000 | 10-20 days | $281.08 |
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N-(tert-Butoxycarbonyl)-L-tyrosine Benzyl Ester
This compound is widely used in peptide synthesis as a protecting group for tyrosine. The tert-butoxycarbonyl (Boc) group safeguards the amino functionality, while the benzyl ester protects the carboxyl group during the synthesis process. It is particularly valuable in solid-phase peptide synthesis (SPPS) where selective deprotection is required to build complex peptides step-by-step. The Boc group can be removed under acidic conditions without affecting the benzyl ester, allowing for precise control over the synthesis. This makes it a crucial reagent in the production of peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and ease of removal under mild conditions make it a preferred choice for protecting tyrosine residues in peptide chains.
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