4-nitro-N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzamide
97%
- Product Code: 83536
CAS:
2293965-52-1
| Molecular Weight: | 368.191 g./mol | Molecular Formula: | C₁₉H₂₁BN₂O₅ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry as an intermediate in the development of boron-containing molecules. Its structure, featuring a tetramethyl dioxaborolane group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the nitro and amide functional groups enhance its reactivity, allowing it to serve as a precursor for further chemical modifications. Its applications also extend to the design of bioactive compounds, particularly in the development of enzyme inhibitors or receptor modulators, where the boronate ester moiety can improve binding affinity and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.005 | 10-20 days | £100.96 |
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| 0.250 | 10-20 days | £310.21 |
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4-nitro-N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzamide
This compound is primarily utilized in organic synthesis and medicinal chemistry as an intermediate in the development of boron-containing molecules. Its structure, featuring a tetramethyl dioxaborolane group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the nitro and amide functional groups enhance its reactivity, allowing it to serve as a precursor for further chemical modifications. Its applications also extend to the design of bioactive compounds, particularly in the development of enzyme inhibitors or receptor modulators, where the boronate ester moiety can improve binding affinity and selectivity.
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