1-Isobutyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
95%
- Product Code: 90408
CAS:
874291-03-9
| Molecular Weight: | 318.2189 g./mol | Molecular Formula: | C₁₇H₂₇BN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09027289 | |
| Melting Point: | Boiling Point: | 415.1 °C at 760 mmHg | |
| Density: | 1.06 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for constructing carbon-carbon bonds in pharmaceutical research. Additionally, it is employed in the development of proteolysis-targeting chimeras (PROTACs), which are innovative therapeutic agents designed to degrade specific disease-causing proteins. Its structural features also make it suitable for use in the preparation of boron-containing compounds, which are increasingly explored for their potential in cancer therapy and imaging applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,277.00 |
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| 1.000 | 10-20 days | ฿6,102.00 |
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1-Isobutyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for constructing carbon-carbon bonds in pharmaceutical research. Additionally, it is employed in the development of proteolysis-targeting chimeras (PROTACs), which are innovative therapeutic agents designed to degrade specific disease-causing proteins. Its structural features also make it suitable for use in the preparation of boron-containing compounds, which are increasingly explored for their potential in cancer therapy and imaging applications.
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