1,1-Diethyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
98%
- Product Code: 89430
CAS:
874290-94-5
| Molecular Weight: | 318.21 g./mol | Molecular Formula: | C₁₇H₂₇BN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08689494 | |
| Melting Point: | 184-186°C | Boiling Point: | 471.3°C |
| Density: | 1.07g/mL | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables efficient Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of boron-containing compounds for potential use in medicinal chemistry, such as enzyme inhibitors or receptor modulators. Its stability and reactivity make it a valuable tool in the design and production of novel bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $330.34 |
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1,1-Diethyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables efficient Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of boron-containing compounds for potential use in medicinal chemistry, such as enzyme inhibitors or receptor modulators. Its stability and reactivity make it a valuable tool in the design and production of novel bioactive molecules.
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