(E)-Ethyl 3-(4-bromophenyl)acrylate

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Reagent Code: #182447
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CAS Number 24393-53-1

science Other reagents with same CAS 24393-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.11 g/mol
Formula C₁₁H₁₁BrO₂
badge Registry Numbers
MDL Number MFCD00012226
thermostat Physical Properties
Boiling Point 308.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and cross-coupling reactions, especially in the development of bioactive molecules. Commonly employed in the preparation of liquid crystals, agrochemicals, and functional materials due to the presence of the bromoaryl group, which allows further functionalization via palladium-catalyzed reactions. Also utilized in research settings for constructing conjugated systems in organic electronic materials.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿1,280.00
inventory 25g
10-20 days ฿6,170.00
inventory 100g
10-20 days ฿24,470.00
inventory 500g
10-20 days ฿107,250.00
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(E)-Ethyl 3-(4-bromophenyl)acrylate
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and cross-coupling reactions, especially in the development of bioactive molecules. Commonly employed in the preparation of liquid crystals, agrochemicals, and functional materials due to the presence of the bromoaryl group, which allows further functionalization via palladium-catalyzed reactions. Also utilized in research settings for c

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and cross-coupling reactions, especially in the development of bioactive molecules. Commonly employed in the preparation of liquid crystals, agrochemicals, and functional materials due to the presence of the bromoaryl group, which allows further functionalization via palladium-catalyzed reactions. Also utilized in research settings for constructing conjugated systems in organic electronic materials.

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