3-tert-butyl-1-[2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea
95%
- Product Code: 80085
CAS:
2246885-97-0
| Molecular Weight: | 332.24546 g./mol | Molecular Formula: | C₁₈H₂₉BN₂O₃ |
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| EC Number: | MDL Number: | MFCD32206561 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of biologically active compounds. Its structure, featuring a urea moiety and a boronate ester group, makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in creating complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl group enhances the stability of the compound, making it suitable for use in various synthetic pathways. Its applications are particularly prominent in the synthesis of targeted drug molecules, where precision and efficiency are critical.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,896.00 |
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| 0.250 | 10-20 days | ฿15,300.00 |
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3-tert-butyl-1-[2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea
This chemical is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of biologically active compounds. Its structure, featuring a urea moiety and a boronate ester group, makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in creating complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl group enhances the stability of the compound, making it suitable for use in various synthetic pathways. Its applications are particularly prominent in the synthesis of targeted drug molecules, where precision and efficiency are critical.
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