Pinacol vinylboronate
98%
- Product Code: 50625
CAS:
75927-49-0
| Molecular Weight: | 154.02 g./mol | Molecular Formula: | C₈H₁₅BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192492 | |
| Melting Point: | Boiling Point: | ||
| Density: | 0.908 g/mL at 25 °C(lit.) | Storage Condition: | 2~8℃ |
Product Description:
Pinacol vinylboronate is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a valuable reagent for introducing vinyl groups into organic molecules, enabling the construction of complex alkenes. This compound is especially useful in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise control over carbon-carbon bond formation is critical. Additionally, it finds application in the preparation of conjugated systems for use in organic electronics and photovoltaics. Its stability and reactivity make it a preferred choice for chemists working on stereoselective transformations and functional group modifications.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| APPEARANCE | Colorless to light yellow liquid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿460.00 |
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| 5.000 | 10-20 days | ฿1,280.00 |
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| 25.000 | 10-20 days | ฿5,330.00 |
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Pinacol vinylboronate
Pinacol vinylboronate is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a valuable reagent for introducing vinyl groups into organic molecules, enabling the construction of complex alkenes. This compound is especially useful in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise control over carbon-carbon bond formation is critical. Additionally, it finds application in the preparation of conjugated systems for use in organic electronics and photovoltaics. Its stability and reactivity make it a preferred choice for chemists working on stereoselective transformations and functional group modifications.
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