2-(4-Methoxyphenyl)malonaldehyde

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Reagent Code: #214583
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CAS Number 65192-28-1

science Other reagents with same CAS 65192-28-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.18 g/mol
Formula C₁₀H₁₀O₃
badge Registry Numbers
MDL Number MFCD00216504
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of flavonoids and other biologically active compounds, particularly in pharmaceuticals and natural product research. Its structure supports condensation reactions, making it valuable in creating heterocyclic systems such as pyrazoles and isoxazoles. Also employed in the development of fluorescent dyes and sensors due to its conjugated aldehyde functionality, which can participate in intramolecular charge transfer processes. Its reactivity allows for use in organic synthesis routes targeting anti-inflammatory and anticancer agents.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25g
10-20 days ฿40,340.00
2-(4-Methoxyphenyl)malonaldehyde
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Used as a key intermediate in the synthesis of flavonoids and other biologically active compounds, particularly in pharmaceuticals and natural product research. Its structure supports condensation reactions, making it valuable in creating heterocyclic systems such as pyrazoles and isoxazoles. Also employed in the development of fluorescent dyes and sensors due to its conjugated aldehyde functionality, which can participate in intramolecular charge transfer processes. Its reactivity allows for use in orga

Used as a key intermediate in the synthesis of flavonoids and other biologically active compounds, particularly in pharmaceuticals and natural product research. Its structure supports condensation reactions, making it valuable in creating heterocyclic systems such as pyrazoles and isoxazoles. Also employed in the development of fluorescent dyes and sensors due to its conjugated aldehyde functionality, which can participate in intramolecular charge transfer processes. Its reactivity allows for use in organic synthesis routes targeting anti-inflammatory and anticancer agents.

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