1,1-Dipropyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
95%
- Product Code: 79944
CAS:
874298-10-9
| Molecular Weight: | 346.27204 g./mol | Molecular Formula: | C₁₉H₃₁BN₂O₃ |
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| EC Number: | MDL Number: | MFCD22494493 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a urea moiety and a boronic ester group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for forming carbon-carbon bonds, enabling the synthesis of complex molecules used in drug discovery and development. Additionally, the boronic ester group can serve as a protective group for boron-containing compounds, which are often employed in targeted drug delivery systems. Its application extends to the preparation of bioactive molecules, including potential anticancer and anti-inflammatory agents, due to its ability to interact with specific biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,842.00 |
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| 0.250 | 10-20 days | ฿18,900.00 |
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1,1-Dipropyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a urea moiety and a boronic ester group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for forming carbon-carbon bonds, enabling the synthesis of complex molecules used in drug discovery and development. Additionally, the boronic ester group can serve as a protective group for boron-containing compounds, which are often employed in targeted drug delivery systems. Its application extends to the preparation of bioactive molecules, including potential anticancer and anti-inflammatory agents, due to its ability to interact with specific biological targets.
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