2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)phenol
98%
- Product Code: 131608
CAS:
1638624-76-6
Molecular Weight: | 288.07 g./mol | Molecular Formula: | C₁₃H₁₆BF₃O₃ |
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EC Number: | MDL Number: | MFCD16994245 | |
Melting Point: | Boiling Point: | 331.1±42.0 °C(Predicted) | |
Density: | 1.23±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily in organic synthesis as a boronic ester reagent for Suzuki-Miyaura cross-coupling reactions. Its phenolic hydroxyl group allows for further functionalization or coordination in catalytic systems, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The presence of the electron-withdrawing trifluoromethyl group enhances reactivity and stability in coupling processes, enabling efficient construction of biaryl compounds. It is also employed in the synthesis of fluorinated organic molecules where controlled molecular architecture is required.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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100mg | 10-20 days | ฿3,900.00 |
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250mg | 10-20 days | ฿6,500.00 |
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1g | 10-20 days | ฿19,500.00 |
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2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)phenol
Used primarily in organic synthesis as a boronic ester reagent for Suzuki-Miyaura cross-coupling reactions. Its phenolic hydroxyl group allows for further functionalization or coordination in catalytic systems, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The presence of the electron-withdrawing trifluoromethyl group enhances reactivity and stability in coupling processes, enabling efficient construction of biaryl compounds. It is also employed in the synthesis of fluorinated organic molecules where controlled molecular architecture is required.
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