Ethyl 3-(2-bromophenyl)acrylate

95%

Reagent Code: #185420
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CAS Number 99134-25-5

science Other reagents with same CAS 99134-25-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.11 g/mol
Formula C₁₁H₁₁BrO₂
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of anti-inflammatory and anticancer agents. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and palladium-catalyzed cross-couplings, enabling the construction of complex organic molecules. Also employed in the preparation of liquid crystal materials and functional polymers due to its conjugated system and ability to undergo polymerization. Commonly utilized in research settings for generating novel heterocyclic compounds through cyclization reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,490.00
inventory 5g
10-20 days ฿6,780.00
inventory 25g
10-20 days ฿27,370.00
Ethyl 3-(2-bromophenyl)acrylate
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Used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of anti-inflammatory and anticancer agents. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and palladium-catalyzed cross-couplings, enabling the construction of complex organic molecules. Also employed in the preparation of liquid crystal materials and functional polymers due to its conjugated system and ability to undergo polymerization. Commonly utilized
Used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of anti-inflammatory and anticancer agents. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and palladium-catalyzed cross-couplings, enabling the construction of complex organic molecules. Also employed in the preparation of liquid crystal materials and functional polymers due to its conjugated system and ability to undergo polymerization. Commonly utilized in research settings for generating novel heterocyclic compounds through cyclization reactions.
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