Triphenylphosphine resin

1% crossl. with DVB, 1.0-1.5 mmol/g, 100-200 mesh

Reagent Code: #240421
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Alias Triphenylphosphine, polymer-bound;
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CAS Number 39319-11-4

science Other reagents with same CAS 39319-11-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.29 g/mol
Formula C₁₈H₁₅P
badge Registry Numbers
MDL Number MFCD00148025
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a solid-supported reagent in organic synthesis, particularly in Wittig reactions where it facilitates the conversion of aldehydes and ketones to alkenes. Its polymeric nature allows for easy separation from reaction mixtures by simple filtration, reducing purification steps. Commonly employed in combinatorial chemistry and parallel synthesis for drug discovery due to its recyclability and compatibility with automated systems. Also utilized in palladium-catalyzed coupling reactions as a phosphine ligand source, enhancing catalyst recovery and stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,820.00
inventory 5g
10-20 days ฿21,830.00

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Triphenylphosphine resin
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Used as a solid-supported reagent in organic synthesis, particularly in Wittig reactions where it facilitates the conversion of aldehydes and ketones to alkenes. Its polymeric nature allows for easy separation from reaction mixtures by simple filtration, reducing purification steps. Commonly employed in combinatorial chemistry and parallel synthesis for drug discovery due to its recyclability and compatibility with automated systems. Also utilized in palladium-catalyzed coupling reactions as a phosphine

Used as a solid-supported reagent in organic synthesis, particularly in Wittig reactions where it facilitates the conversion of aldehydes and ketones to alkenes. Its polymeric nature allows for easy separation from reaction mixtures by simple filtration, reducing purification steps. Commonly employed in combinatorial chemistry and parallel synthesis for drug discovery due to its recyclability and compatibility with automated systems. Also utilized in palladium-catalyzed coupling reactions as a phosphine ligand source, enhancing catalyst recovery and stability.

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