(2-(Difluoromethyl)phenyl)boronic acid
97%
- Product Code: 123597
CAS:
879275-70-4
| Molecular Weight: | 171.94 g./mol | Molecular Formula: | C₇H₇BF₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09864669 | |
| Melting Point: | Boiling Point: | 301.1 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals and agrochemicals. Its difluoromethyl group enhances the stability and reactivity of the boronic acid, making it valuable in the development of bioactive compounds. Additionally, it is employed in materials science for creating advanced polymers and organic electronic materials. Its unique structure allows for precise modifications in molecular design, contributing to innovations in drug discovery and functional materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $919.45 |
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| 0.250 | 10-20 days | $1,315.64 |
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(2-(Difluoromethyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals and agrochemicals. Its difluoromethyl group enhances the stability and reactivity of the boronic acid, making it valuable in the development of bioactive compounds. Additionally, it is employed in materials science for creating advanced polymers and organic electronic materials. Its unique structure allows for precise modifications in molecular design, contributing to innovations in drug discovery and functional materials.
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