N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzo[d]oxazol-2-amine
95%
- Product Code: 50498
CAS:
330793-73-2
| Molecular Weight: | 336.2000 g./mol | Molecular Formula: | C₁₉H₂₁BN₂O₃ |
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| EC Number: | MDL Number: | MFCD17392819 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group serves as a key functional group, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. It is commonly employed in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its benzo[d]oxazol-2-amine moiety contributes to its potential use in the design of fluorescent probes or bioactive compounds due to its electron-rich structure. Researchers also explore its application in polymer chemistry for creating functionalized polymers with specific properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $287.49 |
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N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzo[d]oxazol-2-amine
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group serves as a key functional group, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. It is commonly employed in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its benzo[d]oxazol-2-amine moiety contributes to its potential use in the design of fluorescent probes or bioactive compounds due to its electron-rich structure. Researchers also explore its application in polymer chemistry for creating functionalized polymers with specific properties.
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