2-(1-([1,1'-biphenyl]-4-yl)cyclopropyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 61102
| Molecular Weight: | 320.24 g./mol | Molecular Formula: | C₂₁H₂₅BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, enabling the construction of biaryl structures, which are prevalent in pharmaceuticals, agrochemicals, and materials science. Its stability and reactivity make it a valuable tool in the development of active pharmaceutical ingredients (APIs) and advanced organic materials. Additionally, it is employed in the synthesis of boron-containing compounds, which are useful in various catalytic and medicinal applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White solid |
| PURITY | 94.5-100 |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿17,600.00 |
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| 0.050 | 10-20 days | ฿22,600.00 |
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| 0.250 | 10-20 days | ฿45,200.00 |
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| 1.000 | 10-20 days | ฿72,000.00 |
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| 5.000 | 10-20 days | ฿350,000.00 |
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2-(1-([1,1'-biphenyl]-4-yl)cyclopropyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, enabling the construction of biaryl structures, which are prevalent in pharmaceuticals, agrochemicals, and materials science. Its stability and reactivity make it a valuable tool in the development of active pharmaceutical ingredients (APIs) and advanced organic materials. Additionally, it is employed in the synthesis of boron-containing compounds, which are useful in various catalytic and medicinal applications.
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