3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)benzonitrile
98%
- Product Code: 243533
CAS:
479411-95-5
| Molecular Weight: | 297.09 g./mol | Molecular Formula: | C₁₄H₁₅BF₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12405369 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development. The presence of a nitrile and trifluoromethyl group enhances its utility in creating bioactive molecules with improved metabolic stability and binding affinity. It is particularly useful in the preparation of fluorinated aromatic compounds, which are common motifs in modern medicinal chemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $40.09 |
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| 0.250 | 10-20 days | $71.24 |
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| 1.000 | 10-20 days | $199.23 |
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| 25.000 | 10-20 days | $3,539.62 |
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| 5.000 | 10-20 days | $708.11 |
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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)benzonitrile
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development. The presence of a nitrile and trifluoromethyl group enhances its utility in creating bioactive molecules with improved metabolic stability and binding affinity. It is particularly useful in the preparation of fluorinated aromatic compounds, which are common motifs in modern medicinal chemistry.
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