(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid
98%
- Product Code: 90281
CAS:
380430-62-6
| Molecular Weight: | 301.0592 g./mol | Molecular Formula: | C₁₄H₁₂BNO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03411934 | |
| Melting Point: | 140-148 ℃ | Boiling Point: | 537.1 °C at 760 mmHg |
| Density: | 1.40±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a key intermediate for constructing complex aromatic compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are essential in pharmaceuticals and agrochemicals. Additionally, the benzyloxycarbonyl protecting group enhances its stability during synthetic processes, making it a valuable reagent in multi-step organic transformations. The nitro group further allows for subsequent functionalization, expanding its utility in the development of advanced materials and bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿8,802.00 |
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| 5.000 | 10-20 days | ฿27,792.00 |
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(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid
(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a key intermediate for constructing complex aromatic compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are essential in pharmaceuticals and agrochemicals. Additionally, the benzyloxycarbonyl protecting group enhances its stability during synthetic processes, making it a valuable reagent in multi-step organic transformations. The nitro group further allows for subsequent functionalization, expanding its utility in the development of advanced materials and bioactive molecules.
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