(S)-N-(2-(4-(tert-Butyl)-4,5-dihydrooxazol-2-yl)phenyl)-1-phenylmethanesulfonamide
97%
- Product Code: 113839
CAS:
784194-02-1
| Molecular Weight: | 372.48 g./mol | Molecular Formula: | C₂₀H₂₄N₂O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30536247 | |
| Melting Point: | Boiling Point: | 528.1±60.0°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 as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a sulfonamide group and an oxazoline ring, makes it a valuable building block for developing potential therapeutic agents. It is often employed in the design and optimization of small-molecule inhibitors, particularly those targeting enzymes or receptors involved in disease pathways. Researchers leverage its chiral center to explore stereospecific interactions in drug development, aiming to enhance efficacy and reduce off-target effects. Additionally, it has shown promise in the study of anti-inflammatory and anti-cancer compounds, where its unique chemical framework contributes to the modulation of specific biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿7,380.00 |
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| 1.000 | 10-20 days | ฿14,760.00 |
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(S)-N-(2-(4-(tert-Butyl)-4,5-dihydrooxazol-2-yl)phenyl)-1-phenylmethanesulfonamide
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a sulfonamide group and an oxazoline ring, makes it a valuable building block for developing potential therapeutic agents. It is often employed in the design and optimization of small-molecule inhibitors, particularly those targeting enzymes or receptors involved in disease pathways. Researchers leverage its chiral center to explore stereospecific interactions in drug development, aiming to enhance efficacy and reduce off-target effects. Additionally, it has shown promise in the study of anti-inflammatory and anti-cancer compounds, where its unique chemical framework contributes to the modulation of specific biological targets.
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