N-(tert-Butoxycarbonyl)-β-phenyl-D-phenylalanine
98%
- Product Code: 77629
CAS:
143060-31-5
| Molecular Weight: | 341.40 g./mol | Molecular Formula: | C₆H₅₂CHCHNHCO₂CCH₃₃CO₂H |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191187 | |
| Melting Point: | 157 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Widely utilized in peptide synthesis, it serves as a key building block for introducing phenylalanine derivatives into peptide chains. Its tert-butoxycarbonyl (Boc) protecting group ensures selective deprotection during solid-phase peptide synthesis, enabling precise control over the assembly process. This compound is particularly valuable in creating peptides with specific structural or functional properties, often employed in drug development and biochemical research. Additionally, it aids in the study of enzyme-substrate interactions and the design of peptide-based therapeutics. Its stability and compatibility with various synthetic protocols make it a preferred choice in organic and medicinal chemistry laboratories.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | £323.24 |
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N-(tert-Butoxycarbonyl)-β-phenyl-D-phenylalanine
Widely utilized in peptide synthesis, it serves as a key building block for introducing phenylalanine derivatives into peptide chains. Its tert-butoxycarbonyl (Boc) protecting group ensures selective deprotection during solid-phase peptide synthesis, enabling precise control over the assembly process. This compound is particularly valuable in creating peptides with specific structural or functional properties, often employed in drug development and biochemical research. Additionally, it aids in the study of enzyme-substrate interactions and the design of peptide-based therapeutics. Its stability and compatibility with various synthetic protocols make it a preferred choice in organic and medicinal chemistry laboratories.
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