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  • Ethyltriphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals

    B23096.14
    CAS Number: 1530-32-1See All CAS: 1530-32-1 In Stock

      CAT NUM
      PRODUCT NAME
      Pack Size
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      QUANTITY
       
      CAT NUM: B23096.14
      Ethyltriphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals
      Pack Size: 25GR
      PRICE: 
      CAT NUM: B23096.22
      Ethyltriphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals
      Pack Size: 100GR
      PRICE: 
      CAT NUM: B23096.36
      Ethyltriphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals
      Pack Size: 500GR
      PRICE: 

      CAS Number
      1530-32-1
      Hazard Class
      6.1
      Pack Size
      25GR, 100GR, 500GR
      Molecular Formula
      C20 H20 Br P
      Molecular Weight
      371.26
      MFCD
      00011838
      UN Number
      2811
      Flash Point
      >200
      Storage Temp
      RT
      Brand
      Thermo Scientific - Alfa Aesar

      Ethyltriphenylphosphonium bromide acts as a reactant in the synthesis of D-amino acids from L-cysteine-derived thiazolidines, Leiodolide A through aldol reactions and Horner-Wadsworth-Emmons olefination. It is also used in the preparation of cycloalkanoindolines through diastereoselective intramolecular inimo-ene reactions. Further, it is used as a reagent in solid-state metathesis polycondensation to prepare alkyl-dipropenylthiophene monomers and Mizoroki-Heck cyclization and cascading Tsuji-Trost cyclization reactions.

      This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.


      Applications
      Ethyltriphenylphosphonium bromide acts as a reactant in the synthesis of D-amino acids from L-cysteine-derived thiazolidines, Leiodolide A through aldol reactions and Horner-Wadsworth-Emmons olefination. It is also used in the preparation of cycloalkanoindolines through diastereoselective intramolecular inimo-ene reactions. Further, it is used as a reagent in solid-state metathesis polycondensation to prepare alkyl-dipropenylthiophene monomers and Mizoroki-Heck cyclization and cascading Tsuji-Trost cyclization reactions.

      Solubility
      Soluble in methanol. Slightly soluble in water, acetone and isopropanol.

      Notes
      Hygroscopic. Incompatible with oxidizing agents.
      Certifications
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