Quinoline-6-sulfonyl chloride
98%
- Product Code: 124609
CAS:
65433-99-0
| Molecular Weight: | 227.67 g./mol | Molecular Formula: | C₉H₆ClNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03086095 | |
| Melting Point: | Boiling Point: | 385.826 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Quinoline-6-sulfonyl chloride is widely used as a key intermediate in organic synthesis, particularly in the preparation of sulfonamide derivatives. These derivatives are essential in the development of pharmaceuticals, including antimicrobial and anticancer agents, due to their bioactive properties. It is also employed in the synthesis of dyes and pigments, where its sulfonyl chloride group enables the introduction of sulfonamide functionalities into organic molecules. Additionally, it serves as a reagent in research laboratories for modifying and functionalizing quinoline-based compounds, aiding in the study of their chemical and biological activities. Its role in coupling reactions further makes it valuable for creating complex organic structures in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $752.64 |
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Quinoline-6-sulfonyl chloride
Quinoline-6-sulfonyl chloride is widely used as a key intermediate in organic synthesis, particularly in the preparation of sulfonamide derivatives. These derivatives are essential in the development of pharmaceuticals, including antimicrobial and anticancer agents, due to their bioactive properties. It is also employed in the synthesis of dyes and pigments, where its sulfonyl chloride group enables the introduction of sulfonamide functionalities into organic molecules. Additionally, it serves as a reagent in research laboratories for modifying and functionalizing quinoline-based compounds, aiding in the study of their chemical and biological activities. Its role in coupling reactions further makes it valuable for creating complex organic structures in medicinal chemistry and material science.
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