phenyl 10-methyl-10λ4-acridine-9- carboxylate trifluoromethanesulfonate

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Reagent Code: #225735
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CAS Number 161006-14-0

science Other reagents with same CAS 161006-14-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 463.43 g/mol
Formula C₂₂H₁₆F₃NO₅S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a photoredox catalyst in organic synthesis, enabling light-driven reactions such as C–C and C–N bond formations under mild conditions. Commonly applied in cross-coupling reactions, radical additions, and cyclizations where traditional metal catalysts may fail. Its strong oxidizing power in the excited state allows activation of substrates through single-electron transfer processes. Also employed in materials science for developing photoresponsive systems and in medicinal chemistry for synthesizing complex bioactive molecules. Stable under ambient conditions and compatible with a wide range of functional groups, making it suitable for diverse reaction setups.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿10,080.00
inventory 250mg
10-20 days ฿20,333.50

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phenyl 10-methyl-10λ4-acridine-9- carboxylate trifluoromethanesulfonate
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Used as a photoredox catalyst in organic synthesis, enabling light-driven reactions such as C–C and C–N bond formations under mild conditions. Commonly applied in cross-coupling reactions, radical additions, and cyclizations where traditional metal catalysts may fail. Its strong oxidizing power in the excited state allows activation of substrates through single-electron transfer processes. Also employed in materials science for developing photoresponsive systems and in medicinal chemistry for synthesizin

Used as a photoredox catalyst in organic synthesis, enabling light-driven reactions such as C–C and C–N bond formations under mild conditions. Commonly applied in cross-coupling reactions, radical additions, and cyclizations where traditional metal catalysts may fail. Its strong oxidizing power in the excited state allows activation of substrates through single-electron transfer processes. Also employed in materials science for developing photoresponsive systems and in medicinal chemistry for synthesizing complex bioactive molecules. Stable under ambient conditions and compatible with a wide range of functional groups, making it suitable for diverse reaction setups.

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