Ethyl Di-o-tolylphosphonoacetate

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Reagent Code: #183124
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CAS Number 188945-41-7

science Other reagents with same CAS 188945-41-7

blur_circular Chemical Specifications

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Weight 348.33 g/mol
Formula C₁₈H₂₁O₅P
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MDL Number MFCD01321166
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Storage Room temperature

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Used as a key reagent in organic synthesis, particularly in Horner-Wadsworth-Emmons (HWE) olefination reactions, enabling the efficient formation of carbon-carbon double bonds. Its stabilized phosphonate group facilitates the generation of α,β-unsaturated esters and other olefinic compounds with high stereoselectivity. Commonly applied in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and natural products where precise control over alkene geometry is required. The presence of o-tolyl groups enhances steric and electronic properties, improving reaction yields and selectivity in challenging transformations.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿4,150.00
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Ethyl Di-o-tolylphosphonoacetate
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Used as a key reagent in organic synthesis, particularly in Horner-Wadsworth-Emmons (HWE) olefination reactions, enabling the efficient formation of carbon-carbon double bonds. Its stabilized phosphonate group facilitates the generation of α,β-unsaturated esters and other olefinic compounds with high stereoselectivity. Commonly applied in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and natural products where precise control over alkene geometry is required. The presence of

Used as a key reagent in organic synthesis, particularly in Horner-Wadsworth-Emmons (HWE) olefination reactions, enabling the efficient formation of carbon-carbon double bonds. Its stabilized phosphonate group facilitates the generation of α,β-unsaturated esters and other olefinic compounds with high stereoselectivity. Commonly applied in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and natural products where precise control over alkene geometry is required. The presence of o-tolyl groups enhances steric and electronic properties, improving reaction yields and selectivity in challenging transformations.

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