(2-((diethylamino)methyl)-5-fluorophenyl)boronic acid
98%
- Product Code: 88992
CAS:
1334170-68-1
| Molecular Weight: | 225.06 g./mol | Molecular Formula: | C₁₁H₁₇BFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14687158 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of biologically active compounds. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes, aiding in biochemical research and diagnostics. Its fluorophenyl moiety further enhances its utility in designing compounds with targeted properties.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿30,780.00 |
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(2-((diethylamino)methyl)-5-fluorophenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of biologically active compounds. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes, aiding in biochemical research and diagnostics. Its fluorophenyl moiety further enhances its utility in designing compounds with targeted properties.
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