4-Fluoronaphthalene-1-boronic acid
98%
- Product Code: 90613
CAS:
182344-25-8
| Molecular Weight: | 189.98 g./mol | Molecular Formula: | C₁₀H₈BFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04039221 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds. Additionally, it is employed in the development of fluorescent probes and materials for organic electronics due to its naphthalene backbone, which can impart desirable optical properties.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 240 242? |
| Purity | 97.5 100% |
| APPEARANCE | White solid |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿640.00 |
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| 1.000 | 10-20 days | ฿2,310.00 |
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| 5.000 | 10-20 days | ฿9,330.00 |
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4-Fluoronaphthalene-1-boronic acid
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds. Additionally, it is employed in the development of fluorescent probes and materials for organic electronics due to its naphthalene backbone, which can impart desirable optical properties.
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