2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazole
98%
- Product Code: 115706
CAS:
1229584-17-1
| Molecular Weight: | 270.13 g./mol | Molecular Formula: | C₁₅H₁₉BN₂O₂ |
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| EC Number: | MDL Number: | MFCD18383629 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it finds application in the synthesis of imidazole-containing compounds, which are often explored for their biological activity, including potential use in drug discovery and development. Its stability and reactivity make it a versatile tool in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $443.81 |
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2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazole
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it finds application in the synthesis of imidazole-containing compounds, which are often explored for their biological activity, including potential use in drug discovery and development. Its stability and reactivity make it a versatile tool in medicinal chemistry and material science research.
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