2-(3-((3-Fluorophenoxy)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 41443
CAS:
1648930-12-4
| Molecular Weight: | 328.1855832 g./mol | Molecular Formula: | C₁₉H₂₂BFO₃ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in the field of medicinal chemistry. Its boronic ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of the fluorophenoxy group enhances its potential in designing bioactive molecules, as fluorine atoms often improve metabolic stability and binding affinity in drug candidates. Additionally, its structure can be tailored for use in the development of boron-based probes or sensors for biochemical applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿11,322.00 |
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| 1.000 | 10-20 days | ฿23,292.00 |
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| 5.000 | 10-20 days | ฿70,992.00 |
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2-(3-((3-Fluorophenoxy)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in the field of medicinal chemistry. Its boronic ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of the fluorophenoxy group enhances its potential in designing bioactive molecules, as fluorine atoms often improve metabolic stability and binding affinity in drug candidates. Additionally, its structure can be tailored for use in the development of boron-based probes or sensors for biochemical applications.
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