(E)-4-(4-Bromophenyl)-3-methyl-4-oxobut-2-enoic acid

95%

Reagent Code: #184424
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CAS Number 35504-94-0

science Other reagents with same CAS 35504-94-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.09 g/mol
Formula C₁₁H₉BrO₃
badge Registry Numbers
MDL Number MFCD30472160
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. Its α,β-unsaturated carbonyl structure makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex molecular frameworks. Commonly employed in the development of anti-inflammatory and anticancer agents due to its ability to act as a building block for chalcone derivatives. Also utilized in materials science for synthesizing functionalized aromatic compounds with potential optoelectronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,220.00
inventory 250mg
10-20 days ฿28,390.00
inventory 1g
10-20 days ฿56,780.00

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(E)-4-(4-Bromophenyl)-3-methyl-4-oxobut-2-enoic acid
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. Its α,β-unsaturated carbonyl structure makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex molecular frameworks. Commonly employed in the development of anti-inflammatory and anticancer agents due to its ability to act as a building block for chalcone derivatives. Also utilized in materials science for synthesizing function
Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. Its α,β-unsaturated carbonyl structure makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex molecular frameworks. Commonly employed in the development of anti-inflammatory and anticancer agents due to its ability to act as a building block for chalcone derivatives. Also utilized in materials science for synthesizing functionalized aromatic compounds with potential optoelectronic properties.
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