2-(4-(Furan-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 41565
CAS:
868755-79-7
| Molecular Weight: | 270.1313 g./mol | Molecular Formula: | C₁₆H₁₉BO₃ |
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| EC Number: | MDL Number: | MFCD08435855 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a key intermediate in the development of organic electronic materials, such as OLEDs and organic semiconductors, due to its ability to introduce furan-containing aromatic systems into molecular frameworks. Its stability and reactivity also make it suitable for use in medicinal chemistry for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $355.05 |
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2-(4-(Furan-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a key intermediate in the development of organic electronic materials, such as OLEDs and organic semiconductors, due to its ability to introduce furan-containing aromatic systems into molecular frameworks. Its stability and reactivity also make it suitable for use in medicinal chemistry for drug discovery and development.
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