ethyl 3-oxabicyclo[4.1.0]heptane-7-carboxylate

98%

Reagent Code: #183769

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.21 g/mol
Formula C₉H₁₄O₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and fine chemicals. Its strained bicyclic structure makes it valuable for ring-opening reactions and cycloadditions, enabling the construction of complex molecular frameworks. Commonly employed in the synthesis of bioactive compounds, including potential drug candidates targeting central nervous system disorders and anti-inflammatory agents. Also utilized in the preparation of chiral building blocks for asymmetric synthesis due to its rigid scaffold and functional handle for further modification.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,528.00
inventory 250mg
10-20 days ฿4,752.00

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ethyl 3-oxabicyclo[4.1.0]heptane-7-carboxylate
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and fine chemicals. Its strained bicyclic structure makes it valuable for ring-opening reactions and cycloadditions, enabling the construction of complex molecular frameworks. Commonly employed in the synthesis of bioactive compounds, including potential drug candidates targeting central nervous system disorders and anti-inflammatory agents. Also utilized in the preparation of chiral building blocks for asymm

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and fine chemicals. Its strained bicyclic structure makes it valuable for ring-opening reactions and cycloadditions, enabling the construction of complex molecular frameworks. Commonly employed in the synthesis of bioactive compounds, including potential drug candidates targeting central nervous system disorders and anti-inflammatory agents. Also utilized in the preparation of chiral building blocks for asymmetric synthesis due to its rigid scaffold and functional handle for further modification.

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