N-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzenesulfonamide
95%
- Product Code: 83413
CAS:
2213440-04-9
| Molecular Weight: | 393.6926 g./mol | Molecular Formula: | C₁₈H₂₁BClNO₄S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a dioxaborolane group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. This reaction is crucial in the synthesis of complex molecules, including potential drug candidates.
Additionally, the compound’s benzenesulfonamide moiety suggests potential applications in medicinal chemistry, where sulfonamide derivatives are often explored for their biological activity, such as antimicrobial, anti-inflammatory, or enzyme-inhibiting properties. Researchers may utilize this chemical to design and optimize new therapeutic agents targeting specific diseases.
In material science, its boronate ester group could be leveraged in the development of functional materials, such as sensors or polymers, due to its ability to interact with diols or other functional groups. Overall, this chemical serves as a versatile building block in both pharmaceutical and materials research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿3,474.00 |
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| 0.250 | 10-20 days | ฿9,630.00 |
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| 1.000 | 10-20 days | ฿28,620.00 |
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N-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzenesulfonamide
This chemical is primarily used in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a dioxaborolane group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. This reaction is crucial in the synthesis of complex molecules, including potential drug candidates.
Additionally, the compound’s benzenesulfonamide moiety suggests potential applications in medicinal chemistry, where sulfonamide derivatives are often explored for their biological activity, such as antimicrobial, anti-inflammatory, or enzyme-inhibiting properties. Researchers may utilize this chemical to design and optimize new therapeutic agents targeting specific diseases.
In material science, its boronate ester group could be leveraged in the development of functional materials, such as sensors or polymers, due to its ability to interact with diols or other functional groups. Overall, this chemical serves as a versatile building block in both pharmaceutical and materials research.
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