Boc-N-Me-Leu-OH
97%
- Product Code: 77503
CAS:
53363-89-6
| Molecular Weight: | 245.32 g./mol | Molecular Formula: | CH₃₂CHCH₂CHCOOHNCH₃COOCCH₃₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00038522 | |
| Melting Point: | 55 - 60 °C | Boiling Point: | 338.2 °C at 760 mmHg |
| Density: | Storage Condition: | room temperature |
Product Description:
Boc-N-Me-Leu-OH is widely used in peptide synthesis as a protected amino acid derivative. It serves as a key building block for constructing peptides with specific sequences, particularly when leucine with a methylated nitrogen is required. The Boc (tert-butoxycarbonyl) group protects the amino group during synthesis, ensuring selective reactions at other sites. This compound is essential in medicinal chemistry for developing peptide-based drugs, where precise control over amino acid incorporation is crucial. It is also employed in research to study protein structure and function, as well as in the development of enzyme inhibitors and other bioactive molecules. Its stability and compatibility with various coupling reagents make it a valuable tool in organic and peptide chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿490.00 |
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| 5.000 | 10-20 days | ฿1,910.00 |
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| 25.000 | 10-20 days | ฿8,600.00 |
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Boc-N-Me-Leu-OH
Boc-N-Me-Leu-OH is widely used in peptide synthesis as a protected amino acid derivative. It serves as a key building block for constructing peptides with specific sequences, particularly when leucine with a methylated nitrogen is required. The Boc (tert-butoxycarbonyl) group protects the amino group during synthesis, ensuring selective reactions at other sites. This compound is essential in medicinal chemistry for developing peptide-based drugs, where precise control over amino acid incorporation is crucial. It is also employed in research to study protein structure and function, as well as in the development of enzyme inhibitors and other bioactive molecules. Its stability and compatibility with various coupling reagents make it a valuable tool in organic and peptide chemistry.
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