3-((Diethylamino)methyl)-5-fluorophenylboronic acid
98%
- Product Code: 89954
CAS:
1704066-81-8
| Molecular Weight: | 225.07 g./mol | Molecular Formula: | C₁₁H₁₇BFNO₂ |
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| EC Number: | MDL Number: | MFCD23751277 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceuticals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex molecules, including drug candidates. The presence of the fluorine atom enhances its potential in designing bioactive compounds, as fluorine is often incorporated to improve metabolic stability and binding affinity in drug molecules. Additionally, its diethylamino group can contribute to the solubility and reactivity of the compound in various chemical processes. It is particularly relevant in the synthesis of targeted therapies and enzyme inhibitors, where precise molecular modifications are critical for efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft328,718.04 |
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3-((Diethylamino)methyl)-5-fluorophenylboronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceuticals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex molecules, including drug candidates. The presence of the fluorine atom enhances its potential in designing bioactive compounds, as fluorine is often incorporated to improve metabolic stability and binding affinity in drug molecules. Additionally, its diethylamino group can contribute to the solubility and reactivity of the compound in various chemical processes. It is particularly relevant in the synthesis of targeted therapies and enzyme inhibitors, where precise molecular modifications are critical for efficacy.
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