4-(N,O-Dimethylhydroxylaminocarbonyl)phenylboronic acid
98%
- Product Code: 60913
CAS:
179055-26-6
| Molecular Weight: | 209 g./mol | Molecular Formula: | C₉H₁₂BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04115671 | |
| Melting Point: | 118-124°C | Boiling Point: | 438.2°C |
| Density: | 1.25g/mL | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis as a versatile building block, particularly in cross-coupling reactions. It serves as a key reagent in Suzuki-Miyaura reactions, which are widely employed in the formation of carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is utilized in the preparation of biaryl compounds, which are essential in drug discovery and material science. Its stability and reactivity make it a preferred choice for researchers working on advanced organic transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,400.00 |
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| 5.000 | 10-20 days | ฿4,340.00 |
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4-(N,O-Dimethylhydroxylaminocarbonyl)phenylboronic acid
This chemical is primarily used in organic synthesis as a versatile building block, particularly in cross-coupling reactions. It serves as a key reagent in Suzuki-Miyaura reactions, which are widely employed in the formation of carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is utilized in the preparation of biaryl compounds, which are essential in drug discovery and material science. Its stability and reactivity make it a preferred choice for researchers working on advanced organic transformations.
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