4-Amino-3-fluorophenylboronic acid hydrochloride
97%
- Product Code: 90615
CAS:
1256355-32-4
| Molecular Weight: | 191.4 g./mol | Molecular Formula: | C₆H₈BClFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11867880 | |
| Melting Point: | 150-160 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, airtight, dry |
Product Description:
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes, aiding in biochemical and environmental monitoring. Its fluorine substituent enhances its stability and reactivity, making it a preferred choice in various catalytic and material science applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,391.00 |
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| 1.000 | 10-20 days | ฿13,221.00 |
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4-Amino-3-fluorophenylboronic acid hydrochloride
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes, aiding in biochemical and environmental monitoring. Its fluorine substituent enhances its stability and reactivity, making it a preferred choice in various catalytic and material science applications.
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