(R)-Benzyl 2-amino-3-(3-(methylsulfonyl)phenyl)propanoate hydrochloride
97%
- Product Code: 57094
CAS:
2049127-88-8
| Molecular Weight: | 369.86 g./mol | Molecular Formula: | C₁₇H₂₀ClNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30570304 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring a benzyl ester and a methylsulfonyl group, makes it valuable for designing molecules with specific biological activities. It is often employed in the creation of enzyme inhibitors or receptor modulators, targeting conditions such as inflammation, neurological disorders, or metabolic diseases. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, which is crucial in optimizing drug efficacy and reducing side effects. Researchers also explore its potential in peptide mimetics and prodrug formulations, enhancing drug delivery and stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,744.00 |
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| 0.250 | 10-20 days | ฿5,616.00 |
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| 1.000 | 10-20 days | ฿8,424.00 |
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(R)-Benzyl 2-amino-3-(3-(methylsulfonyl)phenyl)propanoate hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring a benzyl ester and a methylsulfonyl group, makes it valuable for designing molecules with specific biological activities. It is often employed in the creation of enzyme inhibitors or receptor modulators, targeting conditions such as inflammation, neurological disorders, or metabolic diseases. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, which is crucial in optimizing drug efficacy and reducing side effects. Researchers also explore its potential in peptide mimetics and prodrug formulations, enhancing drug delivery and stability.
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