4-[2-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxymethyl]-benzonitrile
98%
- Product Code: 81215
CAS:
2246880-79-3
| Molecular Weight: | 335.2 g./mol | Molecular Formula: | C₂₀H₂₂BNO₃ |
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| EC Number: | MDL Number: | MFCD31614103 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the preparation of complex molecules. It is often employed in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. The presence of the boronate ester group makes it a valuable reagent for coupling with aryl halides, enabling the synthesis of biaryl compounds, which are important in pharmaceuticals, agrochemicals, and materials science. Additionally, its benzonitrile moiety can serve as a functional group for further chemical modifications, making it versatile in the development of advanced organic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,206.00 |
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| 0.250 | 10-20 days | ฿17,010.00 |
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| 1.000 | 10-20 days | ฿34,020.00 |
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4-[2-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxymethyl]-benzonitrile
This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the preparation of complex molecules. It is often employed in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. The presence of the boronate ester group makes it a valuable reagent for coupling with aryl halides, enabling the synthesis of biaryl compounds, which are important in pharmaceuticals, agrochemicals, and materials science. Additionally, its benzonitrile moiety can serve as a functional group for further chemical modifications, making it versatile in the development of advanced organic compounds.
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