4-Fluoro-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzenesulfonamide
95%
- Product Code: 46890
CAS:
1469930-84-4
| Molecular Weight: | 377.2380432 g./mol | Molecular Formula: | C₁₈H₂₁BFNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 489.4±55.0 °C at 760 mmHg | |
| Density: | 1.27±0.1 g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a key intermediate. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of bioactive compounds and materials science research, where its unique structure contributes to the creation of novel polymers and advanced materials. Its sulfonamide moiety also makes it relevant in medicinal chemistry for designing potential drug candidates with specific biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿9,792.00 |
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| 1.000 | 10-20 days | ฿18,792.00 |
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| 5.000 | 10-20 days | ฿56,592.00 |
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4-Fluoro-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzenesulfonamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a key intermediate. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of bioactive compounds and materials science research, where its unique structure contributes to the creation of novel polymers and advanced materials. Its sulfonamide moiety also makes it relevant in medicinal chemistry for designing potential drug candidates with specific biological activities.
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