(1-Cyclopropylvinyl)benzene

≥95%

Reagent Code: #165893
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CAS Number 825-76-3

science Other reagents with same CAS 825-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.21 g/mol
Formula C₁₁H₁₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a specialty intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique vinyl-cyclopropyl structure enables participation in cycloaddition and radical reactions, making it valuable for constructing complex ring systems. It also finds use in polymer chemistry as a monomer for creating functionalized polystyrene derivatives with enhanced thermal or mechanical properties. Due to the strain in the cyclopropyl ring, it can undergo ring-opening reactions under catalytic conditions, allowing for selective carbon-carbon bond formation in advanced synthetic routes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,450.00
inventory 1g
10-20 days ฿37,870.00
inventory 5g
10-20 days ฿160,000.00

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(1-Cyclopropylvinyl)benzene
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Used primarily as a specialty intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique vinyl-cyclopropyl structure enables participation in cycloaddition and radical reactions, making it valuable for constructing complex ring systems. It also finds use in polymer chemistry as a monomer for creating functionalized polystyrene derivatives with enhanced thermal or mechanical properties. Due to the strain in the cyclopropyl ring, it can undergo ring-

Used primarily as a specialty intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique vinyl-cyclopropyl structure enables participation in cycloaddition and radical reactions, making it valuable for constructing complex ring systems. It also finds use in polymer chemistry as a monomer for creating functionalized polystyrene derivatives with enhanced thermal or mechanical properties. Due to the strain in the cyclopropyl ring, it can undergo ring-opening reactions under catalytic conditions, allowing for selective carbon-carbon bond formation in advanced synthetic routes.

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