(5-fluoro-2-(isopropoxymethyl)phenyl)boronic acid
98%
- Product Code: 90882
CAS:
1333392-80-5
| Molecular Weight: | 212.02 g./mol | Molecular Formula: | C₁₀H₁₄BFO₃ |
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| EC Number: | MDL Number: | MFCD14687289 | |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
(5-fluoro-2-(isopropoxymethyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and drug candidates. Its boronic acid group facilitates efficient coupling with aryl halides, enabling the construction of diverse aromatic structures. Additionally, it may be utilized in the development of sensors and diagnostic agents due to its ability to interact with specific biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,765.44 |
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(5-fluoro-2-(isopropoxymethyl)phenyl)boronic acid
(5-fluoro-2-(isopropoxymethyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and drug candidates. Its boronic acid group facilitates efficient coupling with aryl halides, enabling the construction of diverse aromatic structures. Additionally, it may be utilized in the development of sensors and diagnostic agents due to its ability to interact with specific biological targets.
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