(4-(Cyclohexylcarbamoyl)-3-fluorophenyl)boronic acid
97%
- Product Code: 90669
CAS:
874289-11-9
Molecular Weight: | 265.09 g./mol | Molecular Formula: | C₁₃H₁₇BFNO₃ |
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EC Number: | MDL Number: | ||
Melting Point: | 157-159°C | Boiling Point: | |
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its cyclohexyl and fluorine substituents enhance its stability and reactivity, allowing for selective and efficient coupling with various aryl halides. Additionally, it is employed in the development of bioactive compounds and materials science research, where its unique structure contributes to the design of novel polymers and advanced materials.
Product Specification:
Test | Specification |
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APPEARANCE | White to off-white solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿2,410.00 |
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1.000 | 10-20 days | ฿6,280.00 |
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(4-(Cyclohexylcarbamoyl)-3-fluorophenyl)boronic acid
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its cyclohexyl and fluorine substituents enhance its stability and reactivity, allowing for selective and efficient coupling with various aryl halides. Additionally, it is employed in the development of bioactive compounds and materials science research, where its unique structure contributes to the design of novel polymers and advanced materials.
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