2-(4-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)phenyl)-1,1,1-trifluoropropan-2-ol
97%
- Product Code: 115712
CAS:
1467061-57-9
| Molecular Weight: | 302.10 g./mol | Molecular Formula: | C₁₄H₁₈BF₃O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28133801 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex organic molecules.
In medicinal chemistry, it is often used to create biologically active compounds, including potential drug candidates targeting various diseases. The trifluoromethyl group in its structure enhances the metabolic stability and bioavailability of the resulting molecules, making it advantageous in drug design.
Additionally, its application extends to materials science, where it contributes to the synthesis of advanced polymers and organic electronic materials. The unique combination of boronic ester and trifluoromethyl groups allows for the creation of materials with tailored properties, such as improved thermal stability and electronic conductivity.
Overall, this chemical serves as a versatile building block in both life sciences and material sciences, enabling the development of innovative solutions in drug discovery and advanced material design.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,775.00 |
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| 0.250 | 10-20 days | ฿17,541.00 |
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2-(4-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)phenyl)-1,1,1-trifluoropropan-2-ol
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex organic molecules.
In medicinal chemistry, it is often used to create biologically active compounds, including potential drug candidates targeting various diseases. The trifluoromethyl group in its structure enhances the metabolic stability and bioavailability of the resulting molecules, making it advantageous in drug design.
Additionally, its application extends to materials science, where it contributes to the synthesis of advanced polymers and organic electronic materials. The unique combination of boronic ester and trifluoromethyl groups allows for the creation of materials with tailored properties, such as improved thermal stability and electronic conductivity.
Overall, this chemical serves as a versatile building block in both life sciences and material sciences, enabling the development of innovative solutions in drug discovery and advanced material design.
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