4-(N-tert-butylamino)-3-nitrophenylboronic acid pinacol ester
95%
- Product Code: 46408
CAS:
1218791-23-1
| Molecular Weight: | 320.19 g./mol | Molecular Formula: | C₁₆H₂₅BN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13195754 | |
| Melting Point: | Boiling Point: | 429.7±40.0 °C at 760 mmHg | |
| Density: | 1.10±0.1 g/cm3 | Storage Condition: | 2-8℃, dry, airtight |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules. It is particularly valuable in cross-coupling reactions, such as Suzuki-Miyaura couplings, where it facilitates the formation of carbon-carbon bonds. Its boronic ester group enhances stability and reactivity, making it suitable for constructing aromatic systems in pharmaceuticals and agrochemicals. Additionally, it finds application in materials science for developing advanced polymers and functionalized surfaces. Its nitro and tert-butylamino groups contribute to its versatility in selective transformations and modifications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,088.00 |
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| 0.250 | 10-20 days | ฿3,492.00 |
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| 1.000 | 10-20 days | ฿9,144.00 |
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4-(N-tert-butylamino)-3-nitrophenylboronic acid pinacol ester
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules. It is particularly valuable in cross-coupling reactions, such as Suzuki-Miyaura couplings, where it facilitates the formation of carbon-carbon bonds. Its boronic ester group enhances stability and reactivity, making it suitable for constructing aromatic systems in pharmaceuticals and agrochemicals. Additionally, it finds application in materials science for developing advanced polymers and functionalized surfaces. Its nitro and tert-butylamino groups contribute to its versatility in selective transformations and modifications.
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