(4-((2-Methoxyphenyl)carbamoyl)phenyl)boronic acid
98%
- Product Code: 89181
CAS:
1704069-56-6
| Molecular Weight: | 271.08 g./mol | Molecular Formula: | C₁₄H₁₄BNO₄ |
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| EC Number: | MDL Number: | MFCD28384306 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
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 structure, featuring a methoxyphenyl group, enhances its reactivity and selectivity in these reactions, making it valuable for constructing complex organic molecules, such as pharmaceuticals and advanced materials. Additionally, its boronic acid moiety allows it to interact with diols and other Lewis bases, enabling its use in sensor development and biochemical applications, such as glucose sensing or protein labeling. The compound’s stability and compatibility with various reaction conditions further broaden its utility in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿36,640.00 |
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(4-((2-Methoxyphenyl)carbamoyl)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 structure, featuring a methoxyphenyl group, enhances its reactivity and selectivity in these reactions, making it valuable for constructing complex organic molecules, such as pharmaceuticals and advanced materials. Additionally, its boronic acid moiety allows it to interact with diols and other Lewis bases, enabling its use in sensor development and biochemical applications, such as glucose sensing or protein labeling. The compound’s stability and compatibility with various reaction conditions further broaden its utility in medicinal chemistry and material science.
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