2,4,6-Trifluorobenzeneboronic acid
96%
- Product Code: 89557
Alias:
2,4,6-Trifluorophenylboronic acid
CAS:
182482-25-3
Molecular Weight: | 175.9 g./mol | Molecular Formula: | C₆H₄BF₃O₂ |
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EC Number: | MDL Number: | MFCD01863169 | |
Melting Point: | 228-235 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, it serves as a key intermediate in the preparation of pharmaceuticals and agrochemicals. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This property is particularly valuable in the development of complex organic molecules, including drug candidates and advanced materials. Additionally, its trifluorinated aromatic ring enhances its utility in creating compounds with improved stability and bioavailability, making it a versatile reagent in medicinal chemistry and material science.
Product Specification:
Test | Specification |
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PURITYNEUTRALIZATION TITRATION | 95.5 100% |
APPEARANCE | WHITE TO YELLOW CRYSTALS,GRANULES,POWDER, CHUNKS |
INFRARED SPECTRUM | Conforms to Structure |
PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $23.61 |
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5.000 | 10-20 days | $76.34 |
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25.000 | 10-20 days | $339.03 |
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2,4,6-Trifluorobenzeneboronic acid
Used primarily in organic synthesis, it serves as a key intermediate in the preparation of pharmaceuticals and agrochemicals. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This property is particularly valuable in the development of complex organic molecules, including drug candidates and advanced materials. Additionally, its trifluorinated aromatic ring enhances its utility in creating compounds with improved stability and bioavailability, making it a versatile reagent in medicinal chemistry and material science.
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