3,5-Difluorophenylboronic acid
98%
- Product Code: 89931
Alias:
3,5-Difluorophenylboronic acid
CAS:
156545-07-2
| Molecular Weight: | 157.91 g./mol | Molecular Formula: | C₆H₅BF₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318138 | |
| Melting Point: | 210-217 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
3,5-Difluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with aryl boronic acids. Additionally, it is employed in the development of bioactive compounds and drug candidates, where the difluorophenyl moiety can enhance metabolic stability and binding affinity. Its role in materials science includes the creation of organic electronic components and polymers with tailored properties.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 98-100 |
| PURITYNEUTRALIZATION TITRATION | 97.5-102.5 |
| APPEARANCE | Off-white powder |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿450.00 |
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| 25.000 | 10-20 days | ฿1,100.00 |
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| 100.000 | 10-20 days | ฿4,350.00 |
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| 500.000 | 10-20 days | ฿19,400.00 |
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3,5-Difluorophenylboronic acid
3,5-Difluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with aryl boronic acids. Additionally, it is employed in the development of bioactive compounds and drug candidates, where the difluorophenyl moiety can enhance metabolic stability and binding affinity. Its role in materials science includes the creation of organic electronic components and polymers with tailored properties.
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