(3-(Cyclopropylamino)-4,5-difluorophenyl)boronic acid
98%
- Product Code: 65517
CAS:
1704068-53-0
| Molecular Weight: | 212.99 g./mol | Molecular Formula: | C₉H₁₀BF₂NO₂ |
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| EC Number: | MDL Number: | MFCD28384257 | |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
(3-(Cyclopropylamino)-4,5-difluorophenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides or pseudohalides, facilitating the creation of complex biaryl structures. This compound is also explored in medicinal chemistry for its potential in designing bioactive molecules, especially in the development of enzyme inhibitors or receptor modulators due to its unique structural features. Additionally, it may serve as a building block in the synthesis of fluorescent probes or sensors, leveraging its aromatic and functional group properties for specific molecular recognition applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿24,430.00 |
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(3-(Cyclopropylamino)-4,5-difluorophenyl)boronic acid
(3-(Cyclopropylamino)-4,5-difluorophenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides or pseudohalides, facilitating the creation of complex biaryl structures. This compound is also explored in medicinal chemistry for its potential in designing bioactive molecules, especially in the development of enzyme inhibitors or receptor modulators due to its unique structural features. Additionally, it may serve as a building block in the synthesis of fluorescent probes or sensors, leveraging its aromatic and functional group properties for specific molecular recognition applications.
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