2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE

95%

Reagent Code: #240335
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CAS Number 24720-64-7

science Other reagents with same CAS 24720-64-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.35 g/mol
Formula C₂₁H₁₉OP
badge Registry Numbers
MDL Number MFCD00075596
thermostat Physical Properties
Melting Point 219-221 °C(lit.)
Boiling Point 478.5±28.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in Wittig reactions to form α,β-unsaturated carbonyl compounds. It enables the construction of conjugated alkenes by reacting with aldehydes or ketones, making it valuable in the synthesis of complex molecules such as natural products, pharmaceuticals, and fine chemicals. Its phosphorane group facilitates carbon-carbon bond formation under mild conditions, offering good selectivity and yield. Commonly employed in research laboratories for building extended π-systems and in the development of functional organic materials.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿610.00
inventory 5g
10-20 days ฿2,530.00
inventory 25g
10-20 days ฿10,880.00

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2-(TRIPHENYLPHOSPHORANYLIDENE)PROPIONALDEHYDE
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Used as a key intermediate in organic synthesis, particularly in Wittig reactions to form α,β-unsaturated carbonyl compounds. It enables the construction of conjugated alkenes by reacting with aldehydes or ketones, making it valuable in the synthesis of complex molecules such as natural products, pharmaceuticals, and fine chemicals. Its phosphorane group facilitates carbon-carbon bond formation under mild conditions, offering good selectivity and yield. Commonly employed in research laboratories for buil

Used as a key intermediate in organic synthesis, particularly in Wittig reactions to form α,β-unsaturated carbonyl compounds. It enables the construction of conjugated alkenes by reacting with aldehydes or ketones, making it valuable in the synthesis of complex molecules such as natural products, pharmaceuticals, and fine chemicals. Its phosphorane group facilitates carbon-carbon bond formation under mild conditions, offering good selectivity and yield. Commonly employed in research laboratories for building extended π-systems and in the development of functional organic materials.

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