1-benzyl-3-[2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea
95%
- Product Code: 80030
CAS:
2246852-97-9
| Molecular Weight: | 382.26108 g./mol | Molecular Formula: | C₂₁H₂₇BN₂O₄ |
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| EC Number: | MDL Number: | MFCD32206487 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure, featuring a urea moiety and a boronic ester group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the construction of complex organic molecules, including drug candidates. The boronic ester functionality allows for efficient coupling with aryl halides, enabling the formation of carbon-carbon bonds in a controlled manner. Additionally, the benzyl group can provide stability and influence the solubility of the compound, making it suitable for use in various reaction conditions. Its application extends to the synthesis of biologically active compounds, where its structural features can be tailored to enhance drug efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $110.17 |
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| 0.100 | 10-20 days | $329.97 |
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1-benzyl-3-[2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceutical intermediates. Its structure, featuring a urea moiety and a boronic ester group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the construction of complex organic molecules, including drug candidates. The boronic ester functionality allows for efficient coupling with aryl halides, enabling the formation of carbon-carbon bonds in a controlled manner. Additionally, the benzyl group can provide stability and influence the solubility of the compound, making it suitable for use in various reaction conditions. Its application extends to the synthesis of biologically active compounds, where its structural features can be tailored to enhance drug efficacy and selectivity.
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