(6-(2-aminopropan-2-yl)pyridin-3-yl)boronic acid
95%
- Product Code: 91368
CAS:
2225180-57-2
| Molecular Weight: | 180.01202 g./mol | Molecular Formula: | C₈H₁₃BN₂O₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. This functionality is essential in the synthesis of drug candidates, agrochemicals, and advanced materials. Additionally, its pyridine moiety contributes to its stability and reactivity in various catalytic processes, enhancing its utility in medicinal chemistry and material science applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿8,928.00 |
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| 0.100 | 10-20 days | ฿25,200.00 |
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| 0.500 | 10-20 days | ฿55,800.00 |
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(6-(2-aminopropan-2-yl)pyridin-3-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. This functionality is essential in the synthesis of drug candidates, agrochemicals, and advanced materials. Additionally, its pyridine moiety contributes to its stability and reactivity in various catalytic processes, enhancing its utility in medicinal chemistry and material science applications.
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