methyl (E)-4-(1-amino-2-(ethoxycarbonyl)-3-oxobut-1-en-1-yl)benzoate

Reagent Code: #181193
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CAS Number 2128730-54-9

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blur_circular Chemical Specifications

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Weight 291.304 g/mol
Formula C₁₅H₁₇NO₅
inventory_2 Storage & Handling
Storage 2-8°C

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Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and functionalized aromatic systems. Its α,β-unsaturated carbonyl structure with ester and enone functionalities allows participation in Michael addition reactions and cyclocondensations, making it valuable in the development of pharmaceuticals and agrochemicals. It serves in the synthesis of complex molecules where conjugated systems and electron-withdrawing groups facilitate selective transformations. Commonly employed in research settings for constructing carbon-carbon bonds and building multi-substituted ring systems.

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inventory 1g
10-20 days ฿26,600.00

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methyl (E)-4-(1-amino-2-(ethoxycarbonyl)-3-oxobut-1-en-1-yl)benzoate
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Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and functionalized aromatic systems. Its α,β-unsaturated carbonyl structure with ester and enone functionalities allows participation in Michael addition reactions and cyclocondensations, making it valuable in the development of pharmaceuticals and agrochemicals. It serves in the synthesis of complex molecules where conjugated systems and electron-withdrawing groups facilitate selective transformations. C
Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and functionalized aromatic systems. Its α,β-unsaturated carbonyl structure with ester and enone functionalities allows participation in Michael addition reactions and cyclocondensations, making it valuable in the development of pharmaceuticals and agrochemicals. It serves in the synthesis of complex molecules where conjugated systems and electron-withdrawing groups facilitate selective transformations. Commonly employed in research settings for constructing carbon-carbon bonds and building multi-substituted ring systems.
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