(3-(Morpholinomethyl)phenyl)boronic acid
97%
- Product Code: 117641
CAS:
397843-58-2
| Molecular Weight: | 221.06 g./mol | Molecular Formula: | C₁₁H₁₆BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08060623 | |
| Melting Point: | Boiling Point: | 394.6°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, enabling the formation of carbon-carbon bonds in complex organic molecules. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in the synthesis of biaryl compounds, which are essential in drug development. Additionally, it finds applications in material science for the creation of advanced polymers and organic electronic materials. Its morpholine moiety further enhances its solubility and reactivity in various organic solvents, making it a versatile reagent in research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft11,345.14 |
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| 0.250 | 10-20 days | Ft16,581.35 |
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| 1.000 | 10-20 days | Ft39,077.69 |
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| 5.000 | 10-20 days | Ft127,317.63 |
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(3-(Morpholinomethyl)phenyl)boronic acid
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, enabling the formation of carbon-carbon bonds in complex organic molecules. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in the synthesis of biaryl compounds, which are essential in drug development. Additionally, it finds applications in material science for the creation of advanced polymers and organic electronic materials. Its morpholine moiety further enhances its solubility and reactivity in various organic solvents, making it a versatile reagent in research and industrial processes.
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