1-(4-bromophenyl)cyclobutane-1-carbonitrile
90%
- Product Code: 74643
CAS:
485828-58-8
| Molecular Weight: | 236.11 g./mol | Molecular Formula: | C₁₁H₁₀BrN |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 336.236°C at 760 mmHg | |
| Density: | 1.46±0.1 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique cyclobutane ring and bromophenyl group make it valuable in the construction of pharmaceutical compounds, particularly in the design of molecules with potential biological activity. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce the bromophenyl moiety into larger organic frameworks. Additionally, the nitrile group provides a reactive site for further functionalization, enabling the synthesis of amines, carboxylic acids, or heterocycles. Its applications extend to materials science, where it can be used to create polymers or small molecules with specific electronic or optical properties. Researchers also explore its use in agrochemical research for developing novel pesticides or herbicides.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Yellow liquid |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,640.00 |
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| 0.250 | 10-20 days | ฿7,050.00 |
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1-(4-bromophenyl)cyclobutane-1-carbonitrile
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique cyclobutane ring and bromophenyl group make it valuable in the construction of pharmaceutical compounds, particularly in the design of molecules with potential biological activity. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce the bromophenyl moiety into larger organic frameworks. Additionally, the nitrile group provides a reactive site for further functionalization, enabling the synthesis of amines, carboxylic acids, or heterocycles. Its applications extend to materials science, where it can be used to create polymers or small molecules with specific electronic or optical properties. Researchers also explore its use in agrochemical research for developing novel pesticides or herbicides.
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