2-(4-Methylpiperidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine
95%
- Product Code: 41701
CAS:
1402174-21-3
| Molecular Weight: | 303.21 g./mol | Molecular Formula: | C₁₆H₂₆BN₃O₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. The pyrimidine moiety further enhances its versatility, allowing it to serve as a building block in the development of bioactive compounds. Its stability and reactivity make it a preferred choice in medicinal chemistry for designing drug candidates targeting various diseases. Additionally, it finds applications in materials science for synthesizing advanced organic materials with specific electronic or optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $419.49 |
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| 1.000 | 10-20 days | $853.44 |
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| 5.000 | 10-20 days | $2,932.80 |
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2-(4-Methylpiperidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. The pyrimidine moiety further enhances its versatility, allowing it to serve as a building block in the development of bioactive compounds. Its stability and reactivity make it a preferred choice in medicinal chemistry for designing drug candidates targeting various diseases. Additionally, it finds applications in materials science for synthesizing advanced organic materials with specific electronic or optical properties.
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