1-(3-bromophenyl)cyclobutane-1-carbonitrile
≥95%
- Product Code: 74649
CAS:
29786-38-7
| Molecular Weight: | 236.11 g./mol | Molecular Formula: | C₁₁H₁₀BrN |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | 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 structure, featuring a cyclobutane ring and a nitrile group, makes it valuable in the synthesis of pharmaceuticals and agrochemicals. The bromine atom on the phenyl ring allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse derivatives. Additionally, the nitrile group can be transformed into other functional groups, such as carboxylic acids or amines, expanding its utility in drug discovery and material science. Its applications are particularly relevant in the design of molecules with potential biological activity, where the cyclobutane ring can impart specific conformational properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless oil |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿13,510.00 |
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| 1.000 | 10-20 days | ฿28,030.00 |
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| 5.000 | 10-20 days | ฿88,070.00 |
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1-(3-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 structure, featuring a cyclobutane ring and a nitrile group, makes it valuable in the synthesis of pharmaceuticals and agrochemicals. The bromine atom on the phenyl ring allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the creation of diverse derivatives. Additionally, the nitrile group can be transformed into other functional groups, such as carboxylic acids or amines, expanding its utility in drug discovery and material science. Its applications are particularly relevant in the design of molecules with potential biological activity, where the cyclobutane ring can impart specific conformational properties.
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