4-Methyl-3-Nitrophenylboronic Acid
≥98%
- Product Code: 90680
CAS:
80500-27-2
| Molecular Weight: | 180.95 g./mol | Molecular Formula: | C₇H₈BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191550 | |
| Melting Point: | 265-270 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
4-Methyl-3-Nitrophenylboronic Acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, which is a fundamental process in creating complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the production of various bioactive compounds and fine chemicals. Its boronic acid group makes it highly reactive and suitable for coupling with aryl halides, enabling the synthesis of biaryl structures. Additionally, it is utilized in the development of sensors and probes for detecting specific molecules in biochemical research. Its nitro and methyl substituents further enhance its reactivity and selectivity in diverse chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,710.00 |
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4-Methyl-3-Nitrophenylboronic Acid
4-Methyl-3-Nitrophenylboronic Acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, which is a fundamental process in creating complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the production of various bioactive compounds and fine chemicals. Its boronic acid group makes it highly reactive and suitable for coupling with aryl halides, enabling the synthesis of biaryl structures. Additionally, it is utilized in the development of sensors and probes for detecting specific molecules in biochemical research. Its nitro and methyl substituents further enhance its reactivity and selectivity in diverse chemical transformations.
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