(3-Amino-4-fluorophenyl)boronic acid hydrochloride
98%
- Product Code: 89125
CAS:
1704081-06-0
| Molecular Weight: | 191.4 g./mol | Molecular Formula: | C₆H₈BClFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12128735 | |
| Melting Point: | 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, where it acts as a key intermediate for constructing complex molecules. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the presence of the amino and fluorine groups enhances its reactivity and selectivity, enabling its use in the synthesis of biologically active compounds, such as drug candidates targeting specific enzymes or receptors. Its application extends to material science, where it contributes to the creation of functionalized polymers and organic electronics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,410.23 |
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(3-Amino-4-fluorophenyl)boronic acid hydrochloride
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex molecules. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the presence of the amino and fluorine groups enhances its reactivity and selectivity, enabling its use in the synthesis of biologically active compounds, such as drug candidates targeting specific enzymes or receptors. Its application extends to material science, where it contributes to the creation of functionalized polymers and organic electronics.
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