5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-4-amine
95%
- Product Code: 90797
CAS:
2223044-20-8
| Molecular Weight: | 239.07922 g./mol | Molecular Formula: | C₁₀H₁₈BN₃O₃ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and materials science. Its boronate ester group makes it a valuable intermediate for introducing the pyrimidin-4-amine moiety into complex molecules, which is crucial in developing drugs targeting cancer, inflammation, and infectious diseases. Additionally, it serves as a building block in the synthesis of agrochemicals and organic electronic materials, contributing to advancements in crop protection and optoelectronic devices. Its stability and reactivity under mild conditions make it a preferred choice for chemists in various research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿9,612.00 |
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| 0.025 | 10-20 days | ฿21,600.00 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-4-amine
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and materials science. Its boronate ester group makes it a valuable intermediate for introducing the pyrimidin-4-amine moiety into complex molecules, which is crucial in developing drugs targeting cancer, inflammation, and infectious diseases. Additionally, it serves as a building block in the synthesis of agrochemicals and organic electronic materials, contributing to advancements in crop protection and optoelectronic devices. Its stability and reactivity under mild conditions make it a preferred choice for chemists in various research and industrial applications.
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