(2,3-Difluoro-4-(4-methylpiperidin-1-yl)phenyl)boronic acid
98%
- Product Code: 88985
CAS:
1704069-62-4
| Molecular Weight: | 255.07 g./mol | Molecular Formula: | C₁₂H₁₆BF₂NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384261 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of biologically active compounds, such as drugs targeting specific enzymes or receptors. Additionally, it may be employed in material science for the creation of advanced polymers or organic electronic materials, where precise molecular architecture is crucial.
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 | $1,512.87 |
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(2,3-Difluoro-4-(4-methylpiperidin-1-yl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of biologically active compounds, such as drugs targeting specific enzymes or receptors. Additionally, it may be employed in material science for the creation of advanced polymers or organic electronic materials, where precise molecular architecture is crucial.
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