3-Amino-4-fluorobenzeneboronic acid pinacol ester
98%
- Product Code: 90185
CAS:
1003575-43-6
| Molecular Weight: | 237.08 g./mol | Molecular Formula: | C₁₂H₁₇BFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11044430 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex biaryl structures. Its boronic ester group enables efficient coupling with aryl halides, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the fluorine substituent enhances the stability and reactivity of the compound, allowing for selective modifications in drug discovery and development. It is also employed in the preparation of fluorescent probes and sensors due to its ability to interact with specific biological targets.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €71.71 |
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3-Amino-4-fluorobenzeneboronic acid pinacol ester
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex biaryl structures. Its boronic ester group enables efficient coupling with aryl halides, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the fluorine substituent enhances the stability and reactivity of the compound, allowing for selective modifications in drug discovery and development. It is also employed in the preparation of fluorescent probes and sensors due to its ability to interact with specific biological targets.
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