2-Amino-N-(quinolin-8-yl)benzenesulfonamide
95%
- Product Code: 42757
CAS:
16082-64-7
| Molecular Weight: | 299.35 g./mol | Molecular Formula: | C₁₅H₁₃N₃O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring both a quinoline and a sulfonamide moiety, makes it valuable for developing compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers often explore its derivatives for their ability to inhibit specific pathways or interactions in disease models. Additionally, it is studied for its potential use in designing fluorescent probes or sensors due to its aromatic and electron-rich structure, which can interact with biological targets and emit detectable signals.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,037.00 |
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| 0.250 | 10-20 days | ฿14,967.00 |
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2-Amino-N-(quinolin-8-yl)benzenesulfonamide
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring both a quinoline and a sulfonamide moiety, makes it valuable for developing compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers often explore its derivatives for their ability to inhibit specific pathways or interactions in disease models. Additionally, it is studied for its potential use in designing fluorescent probes or sensors due to its aromatic and electron-rich structure, which can interact with biological targets and emit detectable signals.
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