4-Carboxy-3-nitrophenylboronic Acid
98%, containing different amounts of acid anhydride
- Product Code: 90724
CAS:
80500-28-3
| Molecular Weight: | 210.94 g./mol | Molecular Formula: | C₇H₆BNO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10696661 | |
| Melting Point: | 220°C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, this compound serves as a versatile reagent for forming carbon-carbon bonds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex biaryl structures. Its boronic acid group facilitates the coupling with aryl halides, while the nitro and carboxyl groups enhance reactivity and selectivity. Additionally, it finds applications in the development of pharmaceutical intermediates and materials science, where its functional groups allow for further derivatization. Its stability and reactivity make it a useful tool in research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | £71.65 |
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4-Carboxy-3-nitrophenylboronic Acid
Used primarily in organic synthesis, this compound serves as a versatile reagent for forming carbon-carbon bonds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex biaryl structures. Its boronic acid group facilitates the coupling with aryl halides, while the nitro and carboxyl groups enhance reactivity and selectivity. Additionally, it finds applications in the development of pharmaceutical intermediates and materials science, where its functional groups allow for further derivatization. Its stability and reactivity make it a useful tool in research and industrial processes.
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