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  • (Methoxycarbonylmethyl)triphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals

    A16301.14

      CAT NUM
      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: A16301.14
      (Methoxycarbonylmethyl)triphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals
      Pack Size: 25GR
      PRICE: 
      CAT NUM: A16301.22
      (Methoxycarbonylmethyl)triphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals
      Pack Size: 100GR
      PRICE: 
      CAT NUM: A16301.36
      (Methoxycarbonylmethyl)triphenylphosphonium bromide, 98+%, Thermo Scientific Chemicals
      Pack Size: 500GR
      PRICE: 

      CAS Number
      1779-58-4
      Pack Size
      25GR, 100GR, 500GR
      Molecular Formula
      C H3 O2 C C H2 P (C6 H5) 3 Br
      Molecular Weight
      415.28
      MFCD
      00011801
      Storage Temp
      RT
      Brand
      Thermo Scientific - Alfa Aesar

      (Methoxycarbonylmethyl)triphenylphosphonium bromide is a reactant for the synthesis of GSK-3 inhibitors using the Wittig reaction, substituted furanones for antifungal and cytostatic activities, photochromic dithienylethene derivatives, gem-diiodoalkanes containing allylic alcohols and highly substituted cyclopentenes and brazilanes via Au-catalyzed deoxygenative Nazarov cyclization. As reactant for asymmetric hydrogenation of α,β-unsaturated ester-phosphonates, studies of thermal decomposition of phosphonium alkyl ester salts.

      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
      (Methoxycarbonylmethyl)triphenylphosphonium bromide is a reactant for the synthesis of GSK-3 inhibitors using the Wittig reaction, substituted furanones for antifungal and cytostatic activities, photochromic dithienylethene derivatives, gem-diiodoalkanes containing allylic alcohols and highly substituted cyclopentenes and brazilanes via Au-catalyzed deoxygenative Nazarov cyclization. As reactant for asymmetric hydrogenation of α,β-unsaturated ester-phosphonates, studies of thermal decomposition of phosphonium alkyl ester salts.

      Solubility
      Soluble in methanol(almost transparency).

      Notes
      Hygroscopic. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, water, moisture.
      Certifications
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