3-(9-Anthryl)acrolein

98%

Reagent Code: #135485
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CAS Number 38982-12-6

science Other reagents with same CAS 38982-12-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.28 g/mol
Formula C₁₇H₁₂O
badge Registry Numbers
MDL Number MFCD09751223
thermostat Physical Properties
Melting Point 170.0 to 174.0 deg-C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as a fluorescent building block due to the anthracene moiety, enabling detection and tracking in polymer and pharmaceutical research. Serves as a precursor in the preparation of conjugated organic materials for optoelectronic devices such as OLEDs. Also employed in the development of sensors and dyes where light emission and electron delocalization are critical. Its reactivity as an α,β-unsaturated carbonyl compound allows for Michael additions and cycloadditions, making it valuable in constructing complex polycyclic frameworks for medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,980.00
inventory 5g
10-20 days ฿6,000.00
inventory 25g
10-20 days ฿18,650.00

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3-(9-Anthryl)acrolein
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Used in organic synthesis as a fluorescent building block due to the anthracene moiety, enabling detection and tracking in polymer and pharmaceutical research. Serves as a precursor in the preparation of conjugated organic materials for optoelectronic devices such as OLEDs. Also employed in the development of sensors and dyes where light emission and electron delocalization are critical. Its reactivity as an α,β-unsaturated carbonyl compound allows for Michael additions and cycloadditions, making it valu

Used in organic synthesis as a fluorescent building block due to the anthracene moiety, enabling detection and tracking in polymer and pharmaceutical research. Serves as a precursor in the preparation of conjugated organic materials for optoelectronic devices such as OLEDs. Also employed in the development of sensors and dyes where light emission and electron delocalization are critical. Its reactivity as an α,β-unsaturated carbonyl compound allows for Michael additions and cycloadditions, making it valuable in constructing complex polycyclic frameworks for medicinal chemistry.

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