Ethyl 2-benzylidene-3-oxobutanoate

95%

Reagent Code: #182427
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CAS Number 620-80-4

science Other reagents with same CAS 620-80-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.25 g/mol
Formula C₁₃H₁₄O₃
badge Registry Numbers
MDL Number MFCD00521137
thermostat Physical Properties
Boiling Point 296°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of flavonoids and chalcone derivatives, which exhibit biological activities such as anti-inflammatory, antimicrobial, and anticancer properties. It serves as a building block in the synthesis of heterocyclic compounds, including pyrazoles and isoxazoles, due to the reactivity of its conjugated carbonyl and ester functionalities. Its α,β-unsaturated structure allows participation in Michael addition reactions, making it valuable in the development of pharmaceuticals and agrochemicals. Also employed in the fabrication of dyes and UV absorbers owing to its extended π-conjugation system.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿710.00
inventory 1g
10-20 days ฿2,060.00
inventory 5g
10-20 days ฿8,710.00

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Ethyl 2-benzylidene-3-oxobutanoate
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Used as a key intermediate in organic synthesis, particularly in the preparation of flavonoids and chalcone derivatives, which exhibit biological activities such as anti-inflammatory, antimicrobial, and anticancer properties. It serves as a building block in the synthesis of heterocyclic compounds, including pyrazoles and isoxazoles, due to the reactivity of its conjugated carbonyl and ester functionalities. Its α,β-unsaturated structure allows participation in Michael addition reactions, making it valua

Used as a key intermediate in organic synthesis, particularly in the preparation of flavonoids and chalcone derivatives, which exhibit biological activities such as anti-inflammatory, antimicrobial, and anticancer properties. It serves as a building block in the synthesis of heterocyclic compounds, including pyrazoles and isoxazoles, due to the reactivity of its conjugated carbonyl and ester functionalities. Its α,β-unsaturated structure allows participation in Michael addition reactions, making it valuable in the development of pharmaceuticals and agrochemicals. Also employed in the fabrication of dyes and UV absorbers owing to its extended π-conjugation system.

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