N-Fmoc-N-Methyl-beta-alanine
≥97%
- Product Code: 76509
CAS:
172965-84-3
| Molecular Weight: | 325.36 g./mol | Molecular Formula: | C₁₉H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861327 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a building block for constructing peptides with specific structural features. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group is particularly advantageous in solid-phase peptide synthesis, allowing for selective deprotection and subsequent coupling reactions. The N-methyl group introduces conformational constraints, which can enhance the stability and biological activity of the resulting peptides. This makes it valuable in the development of peptide-based drugs, where modifying the peptide backbone can improve pharmacokinetic properties and target specificity. Additionally, it is employed in research to study peptide structure-activity relationships, aiding in the design of novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿387.00 |
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| 1.000 | 10-20 days | ฿954.00 |
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N-Fmoc-N-Methyl-beta-alanine
This compound is primarily utilized in the field of peptide synthesis, where it serves as a building block for constructing peptides with specific structural features. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group is particularly advantageous in solid-phase peptide synthesis, allowing for selective deprotection and subsequent coupling reactions. The N-methyl group introduces conformational constraints, which can enhance the stability and biological activity of the resulting peptides. This makes it valuable in the development of peptide-based drugs, where modifying the peptide backbone can improve pharmacokinetic properties and target specificity. Additionally, it is employed in research to study peptide structure-activity relationships, aiding in the design of novel therapeutic agents.
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