2-(2-(Oxiran-2-yl)ethyl)isoindoline-1,3-dione

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Reagent Code: #222119
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CAS Number 86506-70-9

science Other reagents with same CAS 86506-70-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.22 g/mol
Formula C₁₂H₁₁NO₃
badge Registry Numbers
MDL Number MFCD13192149
thermostat Physical Properties
Boiling Point 359.5±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.353±0.06 g/cm3(Predicted)
Storage 2-8°C, inert atmosphere

description Product Description

Used primarily as a reactive intermediate in organic synthesis, especially in the preparation of epoxy-based resins and polymers. Its epoxide group readily undergoes ring-opening reactions with nucleophiles such as amines and alcohols, making it valuable in crosslinking agents for coatings, adhesives, and composite materials. Commonly employed in the development of high-performance thermosetting systems where thermal stability and mechanical strength are required. Also finds use in modifying epoxy resins to improve toughness and adhesion properties. Due to the phthalimide group, it can act as a protected amine precursor, enabling controlled amine release in specialized synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,940.00
inventory 250mg
10-20 days ฿9,870.00
inventory 1g
10-20 days ฿23,720.00

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2-(2-(Oxiran-2-yl)ethyl)isoindoline-1,3-dione
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Used primarily as a reactive intermediate in organic synthesis, especially in the preparation of epoxy-based resins and polymers. Its epoxide group readily undergoes ring-opening reactions with nucleophiles such as amines and alcohols, making it valuable in crosslinking agents for coatings, adhesives, and composite materials. Commonly employed in the development of high-performance thermosetting systems where thermal stability and mechanical strength are required. Also finds use in modifying epoxy resins

Used primarily as a reactive intermediate in organic synthesis, especially in the preparation of epoxy-based resins and polymers. Its epoxide group readily undergoes ring-opening reactions with nucleophiles such as amines and alcohols, making it valuable in crosslinking agents for coatings, adhesives, and composite materials. Commonly employed in the development of high-performance thermosetting systems where thermal stability and mechanical strength are required. Also finds use in modifying epoxy resins to improve toughness and adhesion properties. Due to the phthalimide group, it can act as a protected amine precursor, enabling controlled amine release in specialized synthetic pathways.

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