(S)-Benzyl 2-amino-3-(3-(methylsulfonyl)phenyl)propanoate hydrochloride
97%
- Product Code: 73954
CAS:
1194550-59-8
| Molecular Weight: | 369.86 g./mol | Molecular Formula: | C₁₇H₂₀ClNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29919305 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). Its structure, featuring a benzyl ester and a methylsulfonyl group, makes it a valuable intermediate in the preparation of biologically active molecules. It is often employed in the design and production of protease inhibitors, which are critical in treating diseases such as HIV and hepatitis C. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, enhancing the efficacy and specificity of therapeutic agents. The compound is also explored in medicinal chemistry for its potential role in targeting specific enzymes or receptors involved in inflammatory and neurological disorders.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to yellow powder or crystals |
| 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 | ฿3,160.00 |
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| 5.000 | 10-20 days | ฿12,490.00 |
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| 10.000 | 10-20 days | ฿21,260.00 |
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| 25.000 | 10-20 days | ฿41,920.00 |
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(S)-Benzyl 2-amino-3-(3-(methylsulfonyl)phenyl)propanoate hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). Its structure, featuring a benzyl ester and a methylsulfonyl group, makes it a valuable intermediate in the preparation of biologically active molecules. It is often employed in the design and production of protease inhibitors, which are critical in treating diseases such as HIV and hepatitis C. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, enhancing the efficacy and specificity of therapeutic agents. The compound is also explored in medicinal chemistry for its potential role in targeting specific enzymes or receptors involved in inflammatory and neurological disorders.
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