1-Phenyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)imidazo[1,5-a]pyridine
98%
- Product Code: 40263
CAS:
2247546-38-7
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| Density: | Storage Condition: | 2-8°C, airtight, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester functional group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is often employed as a key intermediate in the synthesis of complex organic molecules, including heterocyclic compounds. Additionally, its structure is advantageous in medicinal chemistry for designing drug candidates, especially those targeting specific biological pathways. Its stability and reactivity under mild conditions make it a preferred choice in various research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $124.75 |
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| 0.250 | 10-20 days | $383.44 |
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| 1.000 | 10-20 days | $945.09 |
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1-Phenyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)imidazo[1,5-a]pyridine
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester functional group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is often employed as a key intermediate in the synthesis of complex organic molecules, including heterocyclic compounds. Additionally, its structure is advantageous in medicinal chemistry for designing drug candidates, especially those targeting specific biological pathways. Its stability and reactivity under mild conditions make it a preferred choice in various research and industrial applications.
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