Benzylboronic acid pinacol ester
97%
- Product Code: 91202
Alias:
2-Benzyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:
87100-28-5
| Molecular Weight: | 218.1 g./mol | Molecular Formula: | C₁₃H₁₉BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05663841 | |
| Melting Point: | Boiling Point: | 65 °C0.15 mm Hg | |
| Density: | 0.980 g/mL at 25 °C | Storage Condition: | room temperature |
Product Description:
Benzylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex molecules in pharmaceuticals, agrochemicals, and materials science. The compound serves as a stable and reactive boronic ester, facilitating the introduction of benzyl groups into target molecules. Its stability under various conditions makes it a preferred reagent in multi-step synthetic processes. Additionally, it is employed in the development of bioactive compounds and functional materials due to its efficient reactivity and compatibility with diverse reaction conditions.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 97-100 |
| REFRACTIVE INDEX N20D | 1.486-1.49 |
| SPECIFIC GRAVITY 2020C | 0.983-0.987 |
| APPEARANCE | COLORLESS TO PALE YELLOW LIQUID |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft3,232.23 |
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| 5.000 | 10-20 days | Ft11,636.04 |
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| 25.000 | 10-20 days | Ft45,897.70 |
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Benzylboronic acid pinacol ester
Benzylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex molecules in pharmaceuticals, agrochemicals, and materials science. The compound serves as a stable and reactive boronic ester, facilitating the introduction of benzyl groups into target molecules. Its stability under various conditions makes it a preferred reagent in multi-step synthetic processes. Additionally, it is employed in the development of bioactive compounds and functional materials due to its efficient reactivity and compatibility with diverse reaction conditions.
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