(4-((4-(Trifluoromethoxy)phenoxy)methyl)phenyl)boronic acid
98%
- Product Code: 131923
CAS:
870778-97-5
| Molecular Weight: | 312.05 g./mol | Molecular Formula: | C₁₄H₁₂BF₃O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08276770 | |
| Melting Point: | Boiling Point: | 415.5±55.0 °C(Predicted) | |
| Density: | 1.37±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, inert gas |
Product Description:
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceutical and agrochemical development. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for constructing complex aromatic structures. Commonly employed in the preparation of intermediates for bioactive molecules, including potential therapeutics targeting inflammation, cancer, and central nervous system disorders. Also utilized in materials science for designing organic electronic materials due to its stability and reactivity profile.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,140.00 |
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| 1.000 | 10-20 days | ฿10,620.00 |
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| 5.000 | 10-20 days | ฿40,640.00 |
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(4-((4-(Trifluoromethoxy)phenoxy)methyl)phenyl)boronic acid
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceutical and agrochemical development. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for constructing complex aromatic structures. Commonly employed in the preparation of intermediates for bioactive molecules, including potential therapeutics targeting inflammation, cancer, and central nervous system disorders. Also utilized in materials science for designing organic electronic materials due to its stability and reactivity profile.
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