2-Isopropenyl-2-oxazoline

95%

Reagent Code: #200574
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CAS Number 10471-78-0

science Other reagents with same CAS 10471-78-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 111.14 g/mol
Formula C₆H₉NO
badge Registry Numbers
MDL Number MFCD03427229
thermostat Physical Properties
Melting Point −47 °C
Boiling Point 147 °C(Predicted)
inventory_2 Storage & Handling
Density 1.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as a reactive intermediate in polymer chemistry, this compound participates in cationic and radical polymerization processes to form functional polymers with tailored properties. Its vinyl and oxazoline groups enable dual reactivity, making it valuable for creating cross-linked networks or graft copolymers used in coatings, adhesives, and specialty resins. The oxazoline functionality can further react with carboxylic acids or other functional groups, allowing post-polymerization modification for applications in stimuli-responsive materials, drug delivery systems, and compatibilizers in polymer blends. It is also explored in the synthesis of smart materials due to the hydrolytic sensitivity of the oxazoline ring, which can impart degradability or pH-responsiveness to the resulting polymers.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿700.00
inventory 250mg
10-20 days ฿1,480.00
inventory 1g
10-20 days ฿5,910.00

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2-Isopropenyl-2-oxazoline
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Used primarily as a reactive intermediate in polymer chemistry, this compound participates in cationic and radical polymerization processes to form functional polymers with tailored properties. Its vinyl and oxazoline groups enable dual reactivity, making it valuable for creating cross-linked networks or graft copolymers used in coatings, adhesives, and specialty resins. The oxazoline functionality can further react with carboxylic acids or other functional groups, allowing post-polymerization modificati

Used primarily as a reactive intermediate in polymer chemistry, this compound participates in cationic and radical polymerization processes to form functional polymers with tailored properties. Its vinyl and oxazoline groups enable dual reactivity, making it valuable for creating cross-linked networks or graft copolymers used in coatings, adhesives, and specialty resins. The oxazoline functionality can further react with carboxylic acids or other functional groups, allowing post-polymerization modification for applications in stimuli-responsive materials, drug delivery systems, and compatibilizers in polymer blends. It is also explored in the synthesis of smart materials due to the hydrolytic sensitivity of the oxazoline ring, which can impart degradability or pH-responsiveness to the resulting polymers.

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