3-[2-(Trimethylsilyl)ethynyl]benzeneboronic acid pinacol ester
97%
- Product Code: 90106
CAS:
915402-03-8
| Molecular Weight: | 300.28 g./mol | Molecular Formula: | C₁₇H₂₅BO₂Si |
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| EC Number: | MDL Number: | MFCD08706285 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, airtight, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its structure, featuring a boronic ester group and a trimethylsilyl-protected alkyne, makes it a versatile building block for constructing complex molecules. The boronic ester moiety facilitates the formation of carbon-carbon bonds with aryl or vinyl halides, while the protected alkyne can be deprotected and further functionalized. This chemical is valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular architecture is required. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,780.00 |
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3-[2-(Trimethylsilyl)ethynyl]benzeneboronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its structure, featuring a boronic ester group and a trimethylsilyl-protected alkyne, makes it a versatile building block for constructing complex molecules. The boronic ester moiety facilitates the formation of carbon-carbon bonds with aryl or vinyl halides, while the protected alkyne can be deprotected and further functionalized. This chemical is valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular architecture is required. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
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