(5-Fluoro-3-formyl-2-methoxyphenyl)boronic acid
95%
- Product Code: 113336
CAS:
1072951-73-5
| Molecular Weight: | 197.96 g./mol | Molecular Formula: | C₈H₈BFO₄ |
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| EC Number: | MDL Number: | MFCD09265144 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
(5-Fluoro-3-formyl-2-methoxyphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate for the construction of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form carbon-carbon bonds, enabling the synthesis of biaryl compounds. These biaryl structures are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its unique structure, featuring both formyl and boronic acid functional groups, makes it a versatile building block for designing and synthesizing novel compounds with potential biological activity. Its applications extend to medicinal chemistry, where it is used in the discovery and optimization of drug candidates targeting various diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,971.00 |
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| 0.250 | 10-20 days | ฿3,339.00 |
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| 1.000 | 10-20 days | ฿9,000.00 |
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(5-Fluoro-3-formyl-2-methoxyphenyl)boronic acid
(5-Fluoro-3-formyl-2-methoxyphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate for the construction of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form carbon-carbon bonds, enabling the synthesis of biaryl compounds. These biaryl structures are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its unique structure, featuring both formyl and boronic acid functional groups, makes it a versatile building block for designing and synthesizing novel compounds with potential biological activity. Its applications extend to medicinal chemistry, where it is used in the discovery and optimization of drug candidates targeting various diseases.
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