4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)phenol
98%
- Product Code: 46245
CAS:
1243143-45-4
| Molecular Weight: | 288.0706 g./mol | Molecular Formula: | C₁₃H₁₆BF₃O₃ |
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| EC Number: | MDL Number: | MFCD16994250 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key boronic ester intermediate. Its structure, featuring a trifluoromethyl group, enhances its reactivity and selectivity in forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals and agrochemicals. Additionally, the trifluoromethyl group imparts unique properties to the final compounds, such as increased metabolic stability and lipophilicity, which are advantageous in drug development. It is also employed in materials science for the synthesis of advanced organic materials, including polymers and liquid crystals, due to its ability to introduce specific functional groups into complex molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,934.00 |
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)phenol
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key boronic ester intermediate. Its structure, featuring a trifluoromethyl group, enhances its reactivity and selectivity in forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals and agrochemicals. Additionally, the trifluoromethyl group imparts unique properties to the final compounds, such as increased metabolic stability and lipophilicity, which are advantageous in drug development. It is also employed in materials science for the synthesis of advanced organic materials, including polymers and liquid crystals, due to its ability to introduce specific functional groups into complex molecules.
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