4,4a,5,5a,6,6a-Hexahydro-1H-4,6-Ethenocyclopropa[F]Isobenzofuran-1,3(3aH)-Dione

98%

Reagent Code: #197178
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CAS Number 24447-28-7

science Other reagents with same CAS 24447-28-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.2 g/mol
Formula C₁₁H₁₀O₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a reactive intermediate in organic synthesis, especially in the development of complex polycyclic compounds. Its strained ring system makes it valuable in cycloaddition reactions and polymerization processes. Commonly employed in the synthesis of specialty resins and high-performance materials due to its ability to form thermally stable cross-linked structures. Also finds use in research settings for modeling reaction mechanisms involving bridgehead olefins and strained carbocycles.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿15,450.00
1g
10-20 days ฿30,880.00
100mg
10-20 days ฿9,270.00
4,4a,5,5a,6,6a-Hexahydro-1H-4,6-Ethenocyclopropa[F]Isobenzofuran-1,3(3aH)-Dione
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Used primarily as a reactive intermediate in organic synthesis, especially in the development of complex polycyclic compounds. Its strained ring system makes it valuable in cycloaddition reactions and polymerization processes. Commonly employed in the synthesis of specialty resins and high-performance materials due to its ability to form thermally stable cross-linked structures. Also finds use in research settings for modeling reaction mechanisms involving bridgehead olefins and strained carbocycles.

Used primarily as a reactive intermediate in organic synthesis, especially in the development of complex polycyclic compounds. Its strained ring system makes it valuable in cycloaddition reactions and polymerization processes. Commonly employed in the synthesis of specialty resins and high-performance materials due to its ability to form thermally stable cross-linked structures. Also finds use in research settings for modeling reaction mechanisms involving bridgehead olefins and strained carbocycles.

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