1-(4-Chlorobenzyl)-3-(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Urea
95%
- Product Code: 90464
CAS:
874298-88-1
| Molecular Weight: | 386.68016 g./mol | Molecular Formula: | C₂₀H₂₄BClN₂O₃ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a urea moiety and a boronic ester group, makes it valuable in the design of protease inhibitors and other therapeutic agents targeting specific enzymes or proteins. The boronic ester functionality is often leveraged in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex molecules for pharmaceutical applications. Additionally, its potential role in the development of boron-based drugs, such as those targeting cancer or infectious diseases, is an area of active research. Its stability and reactivity make it a useful building block in the creation of novel compounds with potential therapeutic benefits.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | $230.52 |
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| 250mg | 10-20 days | $919.20 |
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1-(4-Chlorobenzyl)-3-(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Urea
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a urea moiety and a boronic ester group, makes it valuable in the design of protease inhibitors and other therapeutic agents targeting specific enzymes or proteins. The boronic ester functionality is often leveraged in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex molecules for pharmaceutical applications. Additionally, its potential role in the development of boron-based drugs, such as those targeting cancer or infectious diseases, is an area of active research. Its stability and reactivity make it a useful building block in the creation of novel compounds with potential therapeutic benefits.
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