N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)phenyl)acetamide
98%
- Product Code: 83342
CAS:
1150271-57-0
| Molecular Weight: | 329.12 g./mol | Molecular Formula: | C₁₅H₁₉BF₃NO₃ |
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| EC Number: | MDL Number: | MFCD12026072 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a tetramethyl dioxaborolane group, makes it a valuable building block for constructing complex molecules, especially in pharmaceutical and agrochemical research. The trifluoromethyl group enhances its stability and reactivity, making it suitable for introducing fluorine-containing moieties into target compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) and advanced materials due to its ability to facilitate precise and efficient bond formation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $92.57 |
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| 0.250 | 10-20 days | $156.81 |
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| 1.000 | 10-20 days | $422.68 |
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N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)phenyl)acetamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a tetramethyl dioxaborolane group, makes it a valuable building block for constructing complex molecules, especially in pharmaceutical and agrochemical research. The trifluoromethyl group enhances its stability and reactivity, making it suitable for introducing fluorine-containing moieties into target compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) and advanced materials due to its ability to facilitate precise and efficient bond formation.
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