(5-(2-Hydroxypropan-2-yl)pyridin-3-yl)boronic acid
95%
- Product Code: 89337
CAS:
1310404-56-8
| Molecular Weight: | 181.00 g./mol | Molecular Formula: | C₈H₁₂BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09992911 | |
| Melting Point: | Boiling Point: | 394.7±52.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of pyridine derivatives, which are valuable in drug discovery and material science. Its stability and reactivity make it a versatile reagent in medicinal chemistry for designing biologically active compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5mg | 10-20 days | $619.68 |
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| 25mg | 10-20 days | $1,817.04 |
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(5-(2-Hydroxypropan-2-yl)pyridin-3-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of pyridine derivatives, which are valuable in drug discovery and material science. Its stability and reactivity make it a versatile reagent in medicinal chemistry for designing biologically active compounds.
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