2,4-Dimethoxyprimidine-5-boronic acid
98%
- Product Code: 89570
Alias:
2,4-Dimethoxypyrimidine-5-boronic acid 2,4-dimethoxy-5-pyrimidineboronic acid
CAS:
89641-18-9
| Molecular Weight: | 183.96 g./mol | Molecular Formula: | C₆H₉BN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318985 | |
| Melting Point: | 113-117 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
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 constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures commonly found in drug molecules. Additionally, it is employed in the synthesis of agrochemicals and materials science applications, where precise molecular design is crucial. Its dimethoxy groups enhance stability and reactivity, making it a valuable reagent in medicinal chemistry for developing potential therapeutic agents.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 98-100 |
| APPEARANCE | White to tan solid |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿850.00 |
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| 5.000 | 10-20 days | ฿2,830.00 |
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| 25.000 | 10-20 days | ฿9,860.00 |
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2,4-Dimethoxyprimidine-5-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 constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures commonly found in drug molecules. Additionally, it is employed in the synthesis of agrochemicals and materials science applications, where precise molecular design is crucial. Its dimethoxy groups enhance stability and reactivity, making it a valuable reagent in medicinal chemistry for developing potential therapeutic agents.
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