Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromide

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Reagent Code: #242953
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CAS Number 61240-20-8

science Other reagents with same CAS 61240-20-8

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Weight 523.40 g/mol
Formula C₂₈H₂₈BrO₃P
badge Registry Numbers
MDL Number MFCD03452736
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a precursor to Wittig reagents in organic synthesis, particularly in the preparation of cyclic compounds and alkenes through Wittig reactions under phase-transfer conditions. It facilitates the formation of carbon-carbon double bonds by converting carbonyl compounds into alkenes under mild conditions. Its trimethoxybenzyl group enhances solubility and reactivity in non-polar solvents, making it effective in solid-liquid and liquid-liquid phase transfer catalysis. Commonly applied in pharmaceutical intermediates synthesis where selective alkene formation is required. Also utilized in the development of functionalized polymers, materials science for constructing conjugated systems, and synthesis of complex natural products like flavonoids or bioactive compounds with aromatic rings and methoxy groups.

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inventory 10mg
10-20 days ฿64,130.00

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Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromide
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Used as a precursor to Wittig reagents in organic synthesis, particularly in the preparation of cyclic compounds and alkenes through Wittig reactions under phase-transfer conditions. It facilitates the formation of carbon-carbon double bonds by converting carbonyl compounds into alkenes under mild conditions. Its trimethoxybenzyl group enhances solubility and reactivity in non-polar solvents, making it effective in solid-liquid and liquid-liquid phase transfer catalysis. Commonly applied in pharmaceutical i
Used as a precursor to Wittig reagents in organic synthesis, particularly in the preparation of cyclic compounds and alkenes through Wittig reactions under phase-transfer conditions. It facilitates the formation of carbon-carbon double bonds by converting carbonyl compounds into alkenes under mild conditions. Its trimethoxybenzyl group enhances solubility and reactivity in non-polar solvents, making it effective in solid-liquid and liquid-liquid phase transfer catalysis. Commonly applied in pharmaceutical intermediates synthesis where selective alkene formation is required. Also utilized in the development of functionalized polymers, materials science for constructing conjugated systems, and synthesis of complex natural products like flavonoids or bioactive compounds with aromatic rings and methoxy groups.
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