2-(4-Methoxyphenyl)-2-oxoacetaldehyde

≥95%

Reagent Code: #213369
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CAS Number 1076-95-5

science Other reagents with same CAS 1076-95-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.16 g/mol
Formula C₉H₈O₃
badge Registry Numbers
MDL Number MFCD00235010
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of flavonoids and heterocyclic compounds with biological activity. It participates in condensation reactions to form chalcone derivatives, which are studied for their antioxidant, anti-inflammatory, and anticancer properties. Also employed in the development of dyes and fluorescent probes due to its conjugated carbonyl structure that enhances light absorption and emission characteristics. Its reactivity makes it valuable in organic synthesis for building complex aromatic systems.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,000.00

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2-(4-Methoxyphenyl)-2-oxoacetaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of flavonoids and heterocyclic compounds with biological activity. It participates in condensation reactions to form chalcone derivatives, which are studied for their antioxidant, anti-inflammatory, and anticancer properties. Also employed in the development of dyes and fluorescent probes due to its conjugated carbonyl structure that enhances light absorption and emission characteristics. Its reactivity makes

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of flavonoids and heterocyclic compounds with biological activity. It participates in condensation reactions to form chalcone derivatives, which are studied for their antioxidant, anti-inflammatory, and anticancer properties. Also employed in the development of dyes and fluorescent probes due to its conjugated carbonyl structure that enhances light absorption and emission characteristics. Its reactivity makes it valuable in organic synthesis for building complex aromatic systems.

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