N-(tert-Butyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
95%
- Product Code: 124213
CAS:
1260231-89-7
Molecular Weight: | 339.26 g./mol | Molecular Formula: | C₁₆H₂₆BNO₄S |
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EC Number: | MDL Number: | MFCD24849675 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. It is particularly useful in the development of bioactive compounds, including potential drug candidates, due to its stability and reactivity. Additionally, it serves as a building block in the synthesis of sulfonamide derivatives, which are widely explored for their therapeutic properties, such as antimicrobial and anti-inflammatory activities. The compound’s structure also lends itself to applications in material science, particularly in the design of organic electronic materials.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | €370.40 |
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N-(tert-Butyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. It is particularly useful in the development of bioactive compounds, including potential drug candidates, due to its stability and reactivity. Additionally, it serves as a building block in the synthesis of sulfonamide derivatives, which are widely explored for their therapeutic properties, such as antimicrobial and anti-inflammatory activities. The compound’s structure also lends itself to applications in material science, particularly in the design of organic electronic materials.
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