2-(Triphenylphosphoranylidene)succinic anhydride

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Reagent Code: #244675
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CAS Number 906-65-0

science Other reagents with same CAS 906-65-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 360.34 g/mol
Formula C₂₂H₁₇O₃P
thermostat Physical Properties
Melting Point 167 °C(lit.)(dec.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a Wittig reagent in organic synthesis, particularly for the conversion of aldehydes into α,β-unsaturated carboxylic acid derivatives. It facilitates the formation of carbon-carbon double bonds with high stereoselectivity, making it valuable in the synthesis of complex molecules such as natural products and pharmaceuticals. Its anhydride functionality allows for further derivatization, enabling the construction of lactones or other cyclic structures through selective ring-opening or condensation reactions. Commonly employed in multi-step synthetic routes where control over double bond geometry and functional group compatibility is essential.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,880.00
inventory 10g
10-20 days ฿13,590.00
inventory 1g
10-20 days ฿1,500.00
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2-(Triphenylphosphoranylidene)succinic anhydride
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Used as a Wittig reagent in organic synthesis, particularly for the conversion of aldehydes into α,β-unsaturated carboxylic acid derivatives. It facilitates the formation of carbon-carbon double bonds with high stereoselectivity, making it valuable in the synthesis of complex molecules such as natural products and pharmaceuticals. Its anhydride functionality allows for further derivatization, enabling the construction of lactones or other cyclic structures through selective ring-opening or condensation r

Used as a Wittig reagent in organic synthesis, particularly for the conversion of aldehydes into α,β-unsaturated carboxylic acid derivatives. It facilitates the formation of carbon-carbon double bonds with high stereoselectivity, making it valuable in the synthesis of complex molecules such as natural products and pharmaceuticals. Its anhydride functionality allows for further derivatization, enabling the construction of lactones or other cyclic structures through selective ring-opening or condensation reactions. Commonly employed in multi-step synthetic routes where control over double bond geometry and functional group compatibility is essential.

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