5-Norbornen-2-yl acetate, mixture of endo and exo

98%

Reagent Code: #216653
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Alias 5-Norectene-2-yl acetate
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CAS Number 6143-29-9

science Other reagents with same CAS 6143-29-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.19 g/mol
Formula C₉H₁₂O₂
badge Registry Numbers
EC Number 228-144-1
MDL Number MFCD00167565
thermostat Physical Properties
Boiling Point 73-76 °C14 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.044 g/mL at 25 °C(lit.)
Storage Room temperature, flammable area

description Product Description

Used primarily as a monomer in copolymerization reactions, especially in the production of specialty polymers with unique thermal and mechanical properties. Its strained norbornene structure enhances reactivity in ring-opening metathesis polymerization (ROMP), making it valuable in creating advanced materials such as high-performance resins, optical films, and photoresists. Also employed in chemical synthesis as a protected diol precursor, where the acetate group can be selectively removed or modified. Its mixture of endo and exo isomers allows for tuning polymer microstructure and material properties. Common in research and development for functional coatings and electronic materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿162.00
25g
10-20 days ฿930.00
100g
10-20 days ฿3,610.00
500g
10-20 days ฿17,330.00
5-Norbornen-2-yl acetate, mixture of endo and exo
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Used primarily as a monomer in copolymerization reactions, especially in the production of specialty polymers with unique thermal and mechanical properties. Its strained norbornene structure enhances reactivity in ring-opening metathesis polymerization (ROMP), making it valuable in creating advanced materials such as high-performance resins, optical films, and photoresists. Also employed in chemical synthesis as a protected diol precursor, where the acetate group can be selectively removed or modified. I

Used primarily as a monomer in copolymerization reactions, especially in the production of specialty polymers with unique thermal and mechanical properties. Its strained norbornene structure enhances reactivity in ring-opening metathesis polymerization (ROMP), making it valuable in creating advanced materials such as high-performance resins, optical films, and photoresists. Also employed in chemical synthesis as a protected diol precursor, where the acetate group can be selectively removed or modified. Its mixture of endo and exo isomers allows for tuning polymer microstructure and material properties. Common in research and development for functional coatings and electronic materials.

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