ethyl (E)-3-(2,4-dimethoxyphenyl)acrylate

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Reagent Code: #183780
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Alias Related CAS: 42174-73-2
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CAS Number 24393-63-3

science Other reagents with same CAS 24393-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.27 g/mol
Formula C₁₃H₁₆O₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Acts as a building block in the preparation of bioactive molecules, particularly in the development of compounds with potential anti-inflammatory and anticancer properties. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex molecular frameworks. Also employed in the synthesis of flavonoid analogs due to the presence of the dimethoxyphenyl moiety, which is common in natural products with biological activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,990.00
inventory 5g
10-20 days ฿29,170.00
inventory 250mg
10-20 days ฿2,690.00
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ethyl (E)-3-(2,4-dimethoxyphenyl)acrylate
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Acts as a building block in the preparation of bioactive molecules, particularly in the development of compounds with potential anti-inflammatory and anticancer properties. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex molecular frameworks. Also employed in the synthesis of flavonoid analogs due to the presence of t

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Acts as a building block in the preparation of bioactive molecules, particularly in the development of compounds with potential anti-inflammatory and anticancer properties. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and other conjugate additions, enabling the construction of complex molecular frameworks. Also employed in the synthesis of flavonoid analogs due to the presence of the dimethoxyphenyl moiety, which is common in natural products with biological activity.

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