Boc-N-Me-Glu(Obzl)-OH
98%
- Product Code: 104828
CAS:
200615-91-4
| Molecular Weight: | 351.39 g./mol | Molecular Formula: | C₁₈H₂₅NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00038756 | |
| Melting Point: | Boiling Point: | 501 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
This chemical is widely used in peptide synthesis as a protected amino acid derivative. Its primary application is in the construction of peptides, where it serves as a building block to introduce glutamic acid residues with specific side-chain protections. The Boc (tert-butoxycarbonyl) group protects the amino group, while the Obzl (benzyl ester) group protects the carboxyl side chain, ensuring selective reactivity during peptide elongation. It is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase methods, enabling the synthesis of complex peptides and proteins. Additionally, it finds use in the development of peptide-based drugs, biomaterials, and research tools, where precise control over amino acid incorporation is essential. Its stability and compatibility with various coupling reagents make it a valuable component in organic and medicinal chemistry workflows.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,698.00 |
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Boc-N-Me-Glu(Obzl)-OH
This chemical is widely used in peptide synthesis as a protected amino acid derivative. Its primary application is in the construction of peptides, where it serves as a building block to introduce glutamic acid residues with specific side-chain protections. The Boc (tert-butoxycarbonyl) group protects the amino group, while the Obzl (benzyl ester) group protects the carboxyl side chain, ensuring selective reactivity during peptide elongation. It is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase methods, enabling the synthesis of complex peptides and proteins. Additionally, it finds use in the development of peptide-based drugs, biomaterials, and research tools, where precise control over amino acid incorporation is essential. Its stability and compatibility with various coupling reagents make it a valuable component in organic and medicinal chemistry workflows.
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