(S)-2-(4-Methylphenylsulfonamido)propanoic acid
97%
- Product Code: 51147
CAS:
21957-58-4
| Molecular Weight: | 243.28 g./mol | Molecular Formula: | C₁₀H₁₃NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02259513 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This chemical is primarily utilized in the pharmaceutical and biochemical research fields. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzyme inhibition. Its structure, featuring a sulfonamide group, makes it valuable in designing drugs that interact with specific proteins or enzymes, often in the context of anti-inflammatory or antimicrobial applications. Researchers also explore its potential in chiral synthesis due to its stereochemistry, which is crucial for producing enantiomerically pure substances. Additionally, it may be used in studies related to metabolic pathways or as a reference standard in analytical chemistry for method development and validation.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off-white to pink Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿290.00 |
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| 1.000 | 10-20 days | ฿350.00 |
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| 5.000 | 10-20 days | ฿940.00 |
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(S)-2-(4-Methylphenylsulfonamido)propanoic acid
This chemical is primarily utilized in the pharmaceutical and biochemical research fields. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzyme inhibition. Its structure, featuring a sulfonamide group, makes it valuable in designing drugs that interact with specific proteins or enzymes, often in the context of anti-inflammatory or antimicrobial applications. Researchers also explore its potential in chiral synthesis due to its stereochemistry, which is crucial for producing enantiomerically pure substances. Additionally, it may be used in studies related to metabolic pathways or as a reference standard in analytical chemistry for method development and validation.
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