2-Cycloheptylideneacetic acid
98%
- Product Code: 131705
CAS:
1903-29-3
| Molecular Weight: | 154.21 g./mol | Molecular Formula: | C₉H₁₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11172853 | |
| Melting Point: | 91 °C | Boiling Point: | 158 °C at 20 mmHg |
| Density: | 1.133±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used primarily as an intermediate in organic synthesis, this compound plays a role in the preparation of cyclic ketones and functionalized alkenes. Its conjugated structure makes it suitable for use in olefination reactions, where it helps form extended carbon-carbon double bonds in complex molecules. It is also employed in the development of specialty chemicals such as fragrances and pharmaceuticals, where the cycloheptyl ring system is a desired structural motif. Due to its reactivity as a Michael acceptor, it participates in cycloaddition and nucleophilic addition reactions, enabling the construction of polycyclic frameworks. Its application in research settings includes probing reaction mechanisms involving carbanions and stabilized enolates.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $138.85 |
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| 0.250 | 10-20 days | $235.21 |
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| 1.000 | 10-20 days | $685.43 |
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2-Cycloheptylideneacetic acid
Used primarily as an intermediate in organic synthesis, this compound plays a role in the preparation of cyclic ketones and functionalized alkenes. Its conjugated structure makes it suitable for use in olefination reactions, where it helps form extended carbon-carbon double bonds in complex molecules. It is also employed in the development of specialty chemicals such as fragrances and pharmaceuticals, where the cycloheptyl ring system is a desired structural motif. Due to its reactivity as a Michael acceptor, it participates in cycloaddition and nucleophilic addition reactions, enabling the construction of polycyclic frameworks. Its application in research settings includes probing reaction mechanisms involving carbanions and stabilized enolates.
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