9-Mesityl-2,7,10-trimethylacridin-10-ium tetrafluoroborate

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Reagent Code: #209804
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CAS Number 1621019-97-3

science Other reagents with same CAS 1621019-97-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 427.2853 g/mol
Formula C₂₅H₂₆BF₄N
badge Registry Numbers
MDL Number MFCD32173817
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a photoredox catalyst in organic synthesis, enabling light-driven reactions such as C–H functionalization, cross-coupling, and radical additions under mild conditions. Its strong oxidizing power in the excited state allows activation of substrates that are otherwise unreactive, making it valuable in pharmaceutical and agrochemical research. Also employed in mechanistic studies to probe electron transfer processes due to its well-defined redox behavior and long excited-state lifetime.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿11,040.00
250mg
10-20 days ฿18,800.00
1g
10-20 days ฿54,930.00

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9-Mesityl-2,7,10-trimethylacridin-10-ium tetrafluoroborate
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Used as a photoredox catalyst in organic synthesis, enabling light-driven reactions such as C–H functionalization, cross-coupling, and radical additions under mild conditions. Its strong oxidizing power in the excited state allows activation of substrates that are otherwise unreactive, making it valuable in pharmaceutical and agrochemical research. Also employed in mechanistic studies to probe electron transfer processes due to its well-defined redox behavior and long excited-state lifetime.

Used as a photoredox catalyst in organic synthesis, enabling light-driven reactions such as C–H functionalization, cross-coupling, and radical additions under mild conditions. Its strong oxidizing power in the excited state allows activation of substrates that are otherwise unreactive, making it valuable in pharmaceutical and agrochemical research. Also employed in mechanistic studies to probe electron transfer processes due to its well-defined redox behavior and long excited-state lifetime.

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