Bis(pinacolato)diboron
98%
- Product Code: 143084
Alias:
Bis(Pinna alcohol combination) diboron; Divaleryl diboron, Pinna alcohol tetraboronate, Bisectal alcohol tetraboron, Bisectal alcohol tetraboron, Bis-3,3-dimethyl-2-butanone diboron; Bisectal alcohol diboron; Related CA No.: 78183-34-3
CAS:
73183-34-3
| Molecular Weight: | 253.94 g./mol | Molecular Formula: | C₁₂H₂₄B₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00799570 | |
| Melting Point: | 137-140 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. It serves as a source of boron, transferring boronate groups to aryl or vinyl halides in the presence of a palladium catalyst. This reactivity makes it valuable in pharmaceutical, agrochemical, and materials science research for constructing complex organic molecules. Its stability and ease of handling enhance its utility in laboratory and industrial settings.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿280.00 |
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| 5g | 10-20 days | ฿450.00 |
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| 25g | 10-20 days | ฿640.00 |
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| 100g | 10-20 days | ฿2,360.00 |
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| 500g | 10-20 days | ฿10,660.00 |
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| 2.5kg | 10-20 days | ฿52,520.00 |
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Bis(pinacolato)diboron
Widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. It serves as a source of boron, transferring boronate groups to aryl or vinyl halides in the presence of a palladium catalyst. This reactivity makes it valuable in pharmaceutical, agrochemical, and materials science research for constructing complex organic molecules. Its stability and ease of handling enhance its utility in laboratory and industrial settings.
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