2,3-Difluoro-4-ethoxyphenylboronic acid
97%
- Product Code: 89894
CAS:
212386-71-5
| Molecular Weight: | 201.97 g./mol | Molecular Formula: | C₈H₉BF₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09258743 | |
| Melting Point: | 151-154℃ | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
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. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the construction of biaryl structures, which are common in many active pharmaceutical ingredients. Its specific substitution pattern, with ethoxy and fluorine groups, allows for fine-tuning of electronic properties, making it valuable in the design of molecules with precise biological activity. Additionally, it is employed in material science for the development of organic electronic materials, where its structural features contribute to desired electronic characteristics.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96.5 100% |
| Appearance | White crystalline |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿783.00 |
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2,3-Difluoro-4-ethoxyphenylboronic 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. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the construction of biaryl structures, which are common in many active pharmaceutical ingredients. Its specific substitution pattern, with ethoxy and fluorine groups, allows for fine-tuning of electronic properties, making it valuable in the design of molecules with precise biological activity. Additionally, it is employed in material science for the development of organic electronic materials, where its structural features contribute to desired electronic characteristics.
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