N-Methyl-D-proline Hydrochloride
95%
- Product Code: 76559
CAS:
702710-17-6
| Molecular Weight: | 165.62 g./mol | Molecular Formula: | C₆H₁₂ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18375303 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
N-Methyl-D-proline Hydrochloride is widely used in the field of peptide synthesis and pharmaceutical research. It serves as a key building block in the development of bioactive peptides and peptidomimetics, which are essential for creating drugs with enhanced stability and specificity. This compound is particularly valuable in the design of peptide-based therapeutics targeting various diseases, including cancer, infectious diseases, and metabolic disorders. Its unique structure allows for the modulation of peptide conformation, improving binding affinity to target proteins. Additionally, it is utilized in the study of enzyme mechanisms and as a chiral auxiliary in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | SOLID |
| PURITY | 95-100 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $41.80 |
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| 5.000 | 10-20 days | $185.98 |
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| 25.000 | 10-20 days | $545.72 |
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N-Methyl-D-proline Hydrochloride
N-Methyl-D-proline Hydrochloride is widely used in the field of peptide synthesis and pharmaceutical research. It serves as a key building block in the development of bioactive peptides and peptidomimetics, which are essential for creating drugs with enhanced stability and specificity. This compound is particularly valuable in the design of peptide-based therapeutics targeting various diseases, including cancer, infectious diseases, and metabolic disorders. Its unique structure allows for the modulation of peptide conformation, improving binding affinity to target proteins. Additionally, it is utilized in the study of enzyme mechanisms and as a chiral auxiliary in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.
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