ethyl 2-bromoacrylate

95%

Reagent Code: #182010
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CAS Number 5459-35-8

science Other reagents with same CAS 5459-35-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.96 g/mol
Formula C₅H₇BrO₂
badge Registry Numbers
MDL Number MFCD02258596
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a building block for pharmaceuticals, agrochemicals, and specialty polymers. Its α,β-unsaturated ester structure with a bromine substituent allows for selective nucleophilic substitution and cross-coupling reactions, making it valuable in the preparation of complex molecules. It is also employed in the synthesis of acrylic-based functional materials where controlled reactivity and polymer modification are required. Due to its electrophilic nature, it participates in Michael addition reactions and can be used to introduce ester and vinyl functionalities in heterocyclic and natural product analogs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,880.00
inventory 1g
10-20 days ฿14,250.00
inventory 5g
10-20 days ฿47,500.00
inventory 10g
10-20 days ฿71,250.00
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ethyl 2-bromoacrylate
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Used primarily as a reactive intermediate in organic synthesis, this compound serves as a building block for pharmaceuticals, agrochemicals, and specialty polymers. Its α,β-unsaturated ester structure with a bromine substituent allows for selective nucleophilic substitution and cross-coupling reactions, making it valuable in the preparation of complex molecules. It is also employed in the synthesis of acrylic-based functional materials where controlled reactivity and polymer modification are required. Du

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a building block for pharmaceuticals, agrochemicals, and specialty polymers. Its α,β-unsaturated ester structure with a bromine substituent allows for selective nucleophilic substitution and cross-coupling reactions, making it valuable in the preparation of complex molecules. It is also employed in the synthesis of acrylic-based functional materials where controlled reactivity and polymer modification are required. Due to its electrophilic nature, it participates in Michael addition reactions and can be used to introduce ester and vinyl functionalities in heterocyclic and natural product analogs.

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