4-nitrophenylboronic acid
≥95%
- Product Code: 90708
CAS:
24067-17-2
| Molecular Weight: | 166.93 g./mol | Molecular Formula: | C₆H₆BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00161360 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃ |
Product Description:
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of biaryl compounds in pharmaceutical and material science research. It acts as a boronic acid derivative in organic synthesis, enabling the formation of carbon-carbon bonds. Additionally, it serves as a building block in the development of sensors for detecting sugars and other diol-containing molecules due to its ability to form reversible covalent bonds with diols. It is also employed in the preparation of advanced materials, such as polymers and metal-organic frameworks, for applications in catalysis and molecular recognition.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 95 100% |
| Appearance | White to brown Crystalline powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿600.00 |
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| 5.000 | 10-20 days | ฿2,950.00 |
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| 25.000 | 10-20 days | ฿13,590.00 |
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4-nitrophenylboronic acid
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of biaryl compounds in pharmaceutical and material science research. It acts as a boronic acid derivative in organic synthesis, enabling the formation of carbon-carbon bonds. Additionally, it serves as a building block in the development of sensors for detecting sugars and other diol-containing molecules due to its ability to form reversible covalent bonds with diols. It is also employed in the preparation of advanced materials, such as polymers and metal-organic frameworks, for applications in catalysis and molecular recognition.
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