Ethyl 2-phenylacrylate

97%

Reagent Code: #182229
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CAS Number 22286-82-4

science Other reagents with same CAS 22286-82-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.22 g/mol
Formula C₁₁H₁₂O₂
badge Registry Numbers
MDL Number MFCD00026862
thermostat Physical Properties
Boiling Point 272.9±19.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a reactive monomer in polymer synthesis, enabling the production of specialty plastics and resins with enhanced rigidity and thermal stability. Commonly employed in coatings, adhesives, and sealants due to its ability to improve adhesion and durability. Also utilized in the development of crosslinking agents for surface modifications and in controlled radical polymerization techniques to create well-defined copolymers. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions in organic synthesis, particularly in pharmaceutical intermediates and fine chemicals.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,400.00
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Ethyl 2-phenylacrylate
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Used primarily as a reactive monomer in polymer synthesis, enabling the production of specialty plastics and resins with enhanced rigidity and thermal stability. Commonly employed in coatings, adhesives, and sealants due to its ability to improve adhesion and durability. Also utilized in the development of crosslinking agents for surface modifications and in controlled radical polymerization techniques to create well-defined copolymers. Its α,β-unsaturated ester structure makes it suitable for Michael addit
Used primarily as a reactive monomer in polymer synthesis, enabling the production of specialty plastics and resins with enhanced rigidity and thermal stability. Commonly employed in coatings, adhesives, and sealants due to its ability to improve adhesion and durability. Also utilized in the development of crosslinking agents for surface modifications and in controlled radical polymerization techniques to create well-defined copolymers. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions in organic synthesis, particularly in pharmaceutical intermediates and fine chemicals.
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