(2-Methylpropyl)boronic acid
95%
- Product Code: 54483
Alias:
(2-Methylpropyl)boronic acid isobutylboronic acid
CAS:
84110-40-7
| Molecular Weight: | 101.94 g./mol | Molecular Formula: | C₄H₁₁BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00134156 | |
| Melting Point: | 108-111 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
(2-Methylpropyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the synthesis of complex organic molecules, enabling the creation of compounds with specific functional properties. Additionally, it is utilized in the development of boron-containing drugs, where its boronic acid group plays a critical role in binding to biological targets. Its stability and reactivity also make it a useful reagent in research and industrial applications for constructing diverse molecular architectures.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 108 112? |
| PURITY TITRATION BY NAOH | 94.5 103.5% |
| APPEARANCE | White to tan powder,crystals and/or chunks |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $14.57 |
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| 5.000 | 10-20 days | $25.11 |
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| 25.000 | 10-20 days | $93.42 |
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(2-Methylpropyl)boronic acid
(2-Methylpropyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the synthesis of complex organic molecules, enabling the creation of compounds with specific functional properties. Additionally, it is utilized in the development of boron-containing drugs, where its boronic acid group plays a critical role in binding to biological targets. Its stability and reactivity also make it a useful reagent in research and industrial applications for constructing diverse molecular architectures.
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