2-Cycloheptylideneacetic acid

98%

Reagent Code: #131705
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CAS Number 1903-29-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.21 g/mol
Formula C₉H₁₄O₂
badge Registry Numbers
MDL Number MFCD11172853
thermostat Physical Properties
Melting Point 91 °C
Boiling Point 158 °C at 20 mmHg
inventory_2 Storage & Handling
Density 1.133±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,680.00
inventory 250mg
10-20 days ฿4,540.00
inventory 1g
10-20 days ฿13,230.00
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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