2-(Trimethylsilyl)ethoxymethyltriphenylphosphonium Chloride

≥98%

Reagent Code: #78347
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CAS Number 82495-75-8

science Other reagents with same CAS 82495-75-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 4291 g/mol
Formula C₂₄H₃₀ClOPSi
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MDL Number MFCD00043159
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description Product Description

This compound is a triphenylphosphonium salt widely used in organic synthesis as a Wittig reagent precursor. It facilitates the stereoselective formation of (E)-1-[2-(trimethylsilyl)ethoxy]alkenes from aldehydes and ketones through olefination reactions, creating carbon-carbon double bonds. These enol ether products serve as protected intermediates in multi-step syntheses, particularly for pharmaceuticals and natural products, where selective manipulation of functional groups is required. Its utility in enhancing synthetic efficiency makes it essential in academic research and industrial applications.

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Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,160.00
inventory 1g
10-20 days ฿890.00

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2-(Trimethylsilyl)ethoxymethyltriphenylphosphonium Chloride
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This compound is a triphenylphosphonium salt widely used in organic synthesis as a Wittig reagent precursor. It facilitates the stereoselective formation of (E)-1-[2-(trimethylsilyl)ethoxy]alkenes from aldehydes and ketones through olefination reactions, creating carbon-carbon double bonds. These enol ether products serve as protected intermediates in multi-step syntheses, particularly for pharmaceuticals and natural products, where selective manipulation of functional groups is required. Its utility in enh
This compound is a triphenylphosphonium salt widely used in organic synthesis as a Wittig reagent precursor. It facilitates the stereoselective formation of (E)-1-[2-(trimethylsilyl)ethoxy]alkenes from aldehydes and ketones through olefination reactions, creating carbon-carbon double bonds. These enol ether products serve as protected intermediates in multi-step syntheses, particularly for pharmaceuticals and natural products, where selective manipulation of functional groups is required. Its utility in enhancing synthetic efficiency makes it essential in academic research and industrial applications.
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