Methyl (E)-4-((4-oxochroman-3-ylidene)methyl)benzoate

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Reagent Code: #181086
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CAS Number 503040-22-0

science Other reagents with same CAS 503040-22-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.3 g/mol
Formula C₁₈H₁₄O₄
thermostat Physical Properties
Boiling Point 487.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.282±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials. Acts as a building block in the development of bioactive compounds due to its α,β-unsaturated carbonyl structure, which supports Michael addition and cycloaddition reactions. Employed in the design of chromone-based derivatives with potential antioxidant, anti-inflammatory, and anticancer activities. Also utilized in the preparation of fluorescent dyes and optoelectronic materials owing to its conjugated system and ability to undergo intramolecular charge transfer.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,730.00
inventory 250mg
10-20 days ฿23,330.00

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Methyl (E)-4-((4-oxochroman-3-ylidene)methyl)benzoate
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Used in organic synthesis as an intermediate for pharmaceuticals and functional materials. Acts as a building block in the development of bioactive compounds due to its α,β-unsaturated carbonyl structure, which supports Michael addition and cycloaddition reactions. Employed in the design of chromone-based derivatives with potential antioxidant, anti-inflammatory, and anticancer activities. Also utilized in the preparation of fluorescent dyes and optoelectronic materials owing to its conjugated system and

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials. Acts as a building block in the development of bioactive compounds due to its α,β-unsaturated carbonyl structure, which supports Michael addition and cycloaddition reactions. Employed in the design of chromone-based derivatives with potential antioxidant, anti-inflammatory, and anticancer activities. Also utilized in the preparation of fluorescent dyes and optoelectronic materials owing to its conjugated system and ability to undergo intramolecular charge transfer.

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