(3,4-Difluoro-5-morpholinophenyl)boronic acid
98%
- Product Code: 89078
CAS:
1704067-18-4
| Molecular Weight: | 243.02 g./mol | Molecular Formula: | C₁₀H₁₂BF₂NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384253 | |
| 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. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group, enabling the coupling with aryl or vinyl halides in the presence of a palladium catalyst. This process is widely employed to create complex organic molecules, including drug intermediates and bioactive compounds. Additionally, its morpholine and difluoro substituents can enhance the stability and reactivity of the resulting products, making it a versatile reagent in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿33,900.00 |
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(3,4-Difluoro-5-morpholinophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group, enabling the coupling with aryl or vinyl halides in the presence of a palladium catalyst. This process is widely employed to create complex organic molecules, including drug intermediates and bioactive compounds. Additionally, its morpholine and difluoro substituents can enhance the stability and reactivity of the resulting products, making it a versatile reagent in medicinal chemistry and material science research.
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