N-(6-BroMo-naphthalen-2-yl)MethanesulfonaMide
≥95%
- Product Code: 50849
CAS:
1132940-86-3
| Molecular Weight: | 300.17 g./mol | Molecular Formula: | C₁₁H₁₀BrNO₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 441.4±37.0℃(Predicted) | |
| Density: | 1.665±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
N-(6-Bromo-naphthalen-2-yl)methanesulfonamide is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly those targeting specific enzymes or receptors. Its structure, featuring a brominated naphthalene ring, makes it valuable for designing molecules with potential therapeutic applications, such as anti-inflammatory or anticancer agents. Additionally, it is employed in the synthesis of complex organic molecules for material science, where its sulfonamide group can enhance stability and reactivity. Researchers also explore its use in creating fluorescent probes or sensors due to its aromatic properties, which can be tailored for specific detection purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,220.00 |
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| 1.000 | 10-20 days | ฿22,815.00 |
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| 5.000 | 10-20 days | ฿68,796.00 |
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N-(6-BroMo-naphthalen-2-yl)MethanesulfonaMide
N-(6-Bromo-naphthalen-2-yl)methanesulfonamide is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly those targeting specific enzymes or receptors. Its structure, featuring a brominated naphthalene ring, makes it valuable for designing molecules with potential therapeutic applications, such as anti-inflammatory or anticancer agents. Additionally, it is employed in the synthesis of complex organic molecules for material science, where its sulfonamide group can enhance stability and reactivity. Researchers also explore its use in creating fluorescent probes or sensors due to its aromatic properties, which can be tailored for specific detection purposes.
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