(4-(N-(tert-Butyl)sulfamoyl)- 2-fluorophenyl)boronic acid
98%
- Product Code: 89261
CAS:
1704097-26-6
Molecular Weight: | 275.1 g./mol | Molecular Formula: | C₁₀H₁₅BFNO₄S |
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Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical research and development. Additionally, the compound's tert-butyl sulfamoyl and fluorine substituents enhance its stability and selectivity in various chemical transformations, contributing to its use in the synthesis of biologically active compounds and advanced materials.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $1,859.25 |
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(4-(N-(tert-Butyl)sulfamoyl)- 2-fluorophenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical research and development. Additionally, the compound's tert-butyl sulfamoyl and fluorine substituents enhance its stability and selectivity in various chemical transformations, contributing to its use in the synthesis of biologically active compounds and advanced materials.
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