(S)-5-Phenyl-1H-pyrrol-3-yl 2-(4-methylphenylsulfonamido)propanoate
≥95%
- Product Code: 117489
CAS:
99740-00-8
| Molecular Weight: | 384.45 g./mol | Molecular Formula: | C₂₀H₂₀N₂O₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08704359 | |
| Melting Point: | 153-155°C | Boiling Point: | 613.3°C at 760 mmHg |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a phenylpyrrole moiety and a sulfonamido group, makes it valuable for developing compounds with potential therapeutic applications, particularly in targeting enzyme inhibition or receptor modulation. Researchers often explore its use in designing drugs for conditions such as inflammation, cancer, or neurological disorders due to its ability to interact with specific biological pathways. Additionally, its chiral center allows for the study of stereospecific interactions, enhancing the precision of drug development.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,290.00 |
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| 1.000 | 10-20 days | ฿9,300.00 |
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| 5.000 | 10-20 days | ฿33,070.00 |
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(S)-5-Phenyl-1H-pyrrol-3-yl 2-(4-methylphenylsulfonamido)propanoate
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a phenylpyrrole moiety and a sulfonamido group, makes it valuable for developing compounds with potential therapeutic applications, particularly in targeting enzyme inhibition or receptor modulation. Researchers often explore its use in designing drugs for conditions such as inflammation, cancer, or neurological disorders due to its ability to interact with specific biological pathways. Additionally, its chiral center allows for the study of stereospecific interactions, enhancing the precision of drug development.
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