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  • Triphosgene, 98%, Thermo Scientific Chemicals

    A14932.06
    CAS Number: 32315-10-9See All CAS: 32315-10-9 In Stock

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      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: A14932.06
      Triphosgene, 98%, Thermo Scientific Chemicals
      Pack Size: 5GR
      PRICE: 
      CAT NUM: A14932.14
      Triphosgene, 98%, Thermo Scientific Chemicals
      Pack Size: 25GR
      PRICE: 
      CAT NUM: A14932.22
      Triphosgene, 98%, Thermo Scientific Chemicals
      Pack Size: 100GR
      PRICE: 

      CAS Number
      32315-10-9
      Hazard Class
      6.1
      Pack Size
      5GR, 25GR, 100GR
      Molecular Formula
      C3 Cl6 O3
      Molecular Weight
      296.75
      MFCD
      00062848
      Density
      1.6
      UN Number
      2928
      Storage Temp
      Refrigerator +4°C
      Brand
      Thermo Scientific - Alfa Aesar

      Triphosgene is used as a carbonylating agent for aza-peptide synthesis. It reacts with several alfa-amino acids to give the corresponding N-carboxyanhydrides. It is involved in the preparation of the esterification coupling reagent, di-2-thienyl carbonate from 2(5H)-thiophenone. Further, it is used as a reagent in organic synthesis and converts an amino group into isocyanate. In addition to this, it is employed in the preparation of 2-chloronicotinaldehydes through cyclization of the corresponding enamides. It is considered as a useful substitute for phosgene.

      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
      Triphosgene is used as a carbonylating agent for aza-peptide synthesis. It reacts with several alfa-amino acids to give the corresponding N-carboxyanhydrides. It is involved in the preparation of the esterification coupling reagent, di-2-thienyl carbonate from 2(5H)-thiophenone. Further, it is used as a reagent in organic synthesis and converts an amino group into isocyanate. In addition to this, it is employed in the preparation of 2-chloronicotinaldehydes through cyclization of the corresponding enamides. It is considered as a useful substitute for phosgene.

      Solubility
      Soluble in ether, ethanol, tetrahydrofuran, benzene, cyclohexane, chloroform, hexane, carbon tetrachloride, dichloromethane and chlorobenzene. Insoluble in water.

      Notes
      Moisture sensitive. Store in a cool place. Incompatible with oxidizing agents.
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