1-(4-fluorophenyl)-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
95%
- Product Code: 89988
CAS:
874301-65-2
| Molecular Weight: | 356.2 g./mol | Molecular Formula: | C₁₉H₂₂BFN₂O₃ |
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| EC Number: | MDL Number: | MFCD22494545 | |
| Melting Point: | Boiling Point: | ||
| 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 boronate ester group, makes it valuable for constructing compounds with potential therapeutic applications. The boronate ester group is often employed in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals. Additionally, the presence of the fluorophenyl group can enhance the metabolic stability and binding affinity of the resulting compounds, making it useful in the design of drugs targeting specific proteins or enzymes. Its applications are particularly relevant in the development of kinase inhibitors, which are important in cancer therapy and other disease treatments.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿5,391.00 |
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| 0.250 | 10-20 days | ฿21,582.00 |
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1-(4-fluorophenyl)-3-(3-(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 boronate ester group, makes it valuable for constructing compounds with potential therapeutic applications. The boronate ester group is often employed in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals. Additionally, the presence of the fluorophenyl group can enhance the metabolic stability and binding affinity of the resulting compounds, making it useful in the design of drugs targeting specific proteins or enzymes. Its applications are particularly relevant in the development of kinase inhibitors, which are important in cancer therapy and other disease treatments.
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