Pinacol 4-(3-methoxyphenyl urea) phenylboronic acid pinacol ester
95%
- Product Code: 46232
CAS:
1669414-60-1
| Molecular Weight: | 368.2345 g./mol | Molecular Formula: | C₂₀H₂₅BN₂O₄ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic ester functional group, which is highly valuable in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal in constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a methoxyphenyl urea moiety, may also contribute to its potential use in designing bioactive compounds or enzyme inhibitors, particularly in medicinal chemistry. Additionally, the pinacol ester group enhances stability, making it suitable for storage and handling in various chemical processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,028.00 |
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| 0.250 | 10-20 days | ฿13,392.00 |
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| 1.000 | 10-20 days | ฿32,292.00 |
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Pinacol 4-(3-methoxyphenyl urea) phenylboronic acid pinacol ester
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic ester functional group, which is highly valuable in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal in constructing carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a methoxyphenyl urea moiety, may also contribute to its potential use in designing bioactive compounds or enzyme inhibitors, particularly in medicinal chemistry. Additionally, the pinacol ester group enhances stability, making it suitable for storage and handling in various chemical processes.
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