t-Butyloxycarbonyl-valyl-alanyl-4-aminobenzylalcohol N-[(2-Methyl-2-propanyl)oxy]carbonyl-L-valyl-N-[4-(hydroxymethyl)phenyl]-L-alaninamide
95%
- Product Code: 121671
CAS:
1884577-99-4
| Molecular Weight: | 393.5 g./mol | Molecular Formula: | C₂₀H₃₁N₃O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28557280 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily used in peptide synthesis as a protecting group for amino acids. It helps in the selective deprotection of specific functional groups during the synthesis of complex peptides, ensuring the desired sequence is achieved without unwanted side reactions. Its structure allows for stability under various reaction conditions, making it suitable for use in solid-phase peptide synthesis. Additionally, it is employed in the development of pharmaceuticals, particularly in the creation of peptide-based drugs, where precise control over amino acid coupling is essential. Its role in protecting the amine group of valine and alanine derivatives is crucial for maintaining the integrity of the peptide chain during synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿61,776.00 |
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t-Butyloxycarbonyl-valyl-alanyl-4-aminobenzylalcohol N-[(2-Methyl-2-propanyl)oxy]carbonyl-L-valyl-N-[4-(hydroxymethyl)phenyl]-L-alaninamide
This compound is primarily used in peptide synthesis as a protecting group for amino acids. It helps in the selective deprotection of specific functional groups during the synthesis of complex peptides, ensuring the desired sequence is achieved without unwanted side reactions. Its structure allows for stability under various reaction conditions, making it suitable for use in solid-phase peptide synthesis. Additionally, it is employed in the development of pharmaceuticals, particularly in the creation of peptide-based drugs, where precise control over amino acid coupling is essential. Its role in protecting the amine group of valine and alanine derivatives is crucial for maintaining the integrity of the peptide chain during synthesis.
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