(4-(Hexylcarbamoyl)phenyl)boronic acid
95%
- Product Code: 46523
CAS:
1611473-73-4
| Molecular Weight: | 249.1138 g./mol | Molecular Formula: | C₁₃H₂₀BNO₃ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its hexylcarbamoyl group enhances solubility in organic solvents, making it suitable for reactions in non-aqueous environments. It is also employed in the development of pharmaceuticals and agrochemicals, where it serves as a key intermediate for constructing complex molecules. Additionally, its boronic acid moiety is valuable in the design of sensors and probes for detecting sugars and other diol-containing compounds, leveraging its ability to form reversible complexes with such molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿8,352.00 |
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| 1.000 | 10-20 days | ฿16,992.00 |
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| 5.000 | 10-20 days | ฿65,592.00 |
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(4-(Hexylcarbamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its hexylcarbamoyl group enhances solubility in organic solvents, making it suitable for reactions in non-aqueous environments. It is also employed in the development of pharmaceuticals and agrochemicals, where it serves as a key intermediate for constructing complex molecules. Additionally, its boronic acid moiety is valuable in the design of sensors and probes for detecting sugars and other diol-containing compounds, leveraging its ability to form reversible complexes with such molecules.
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