1-(4-fluorobenzyl)-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
95%
- Product Code: 79980
CAS:
874301-88-9
| Molecular Weight: | 370.22556 g./mol | Molecular Formula: | C₂₀H₂₄BFN₂O₃ |
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| EC Number: | MDL Number: | MFCD22494690 | |
| 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 in the synthesis of biologically active molecules. Its structure, featuring a urea linkage and a boronate ester group, makes it a valuable intermediate in the preparation of targeted therapies, especially for diseases like cancer and inflammatory disorders. The boronate ester moiety is crucial for Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex molecules. Additionally, the presence of the fluorobenzyl group enhances the compound's ability to interact with biological targets, improving its potential as a precursor for developing enzyme inhibitors or receptor modulators. Its applications are also explored in the development of boron-containing drugs, which are gaining attention for their therapeutic potential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿5,292.00 |
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| 0.250 | 10-20 days | ฿21,150.00 |
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1-(4-fluorobenzyl)-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 in the synthesis of biologically active molecules. Its structure, featuring a urea linkage and a boronate ester group, makes it a valuable intermediate in the preparation of targeted therapies, especially for diseases like cancer and inflammatory disorders. The boronate ester moiety is crucial for Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex molecules. Additionally, the presence of the fluorobenzyl group enhances the compound's ability to interact with biological targets, improving its potential as a precursor for developing enzyme inhibitors or receptor modulators. Its applications are also explored in the development of boron-containing drugs, which are gaining attention for their therapeutic potential.
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