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  • (S)-(-)-2-Methyl-2-propanesulfinamide, 97%, Thermo Scientific Chemicals

    H27115.03
    CAS Number: 343338-28-3See All CAS: 343338-28-3 In Stock

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      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: H27115.03
      (S)-(-)-2-Methyl-2-propanesulfinamide, 97%, Thermo Scientific Chemicals
      Pack Size: 1GR
      PRICE: 
      CAT NUM: H27115.06
      (S)-(-)-2-Methyl-2-propanesulfinamide, 97%, Thermo Scientific Chemicals
      Pack Size: 5GR
      PRICE: 
      CAT NUM: H27115.14
      (S)-(-)-2-Methyl-2-propanesulfinamide, 97%, Thermo Scientific Chemicals
      Pack Size: 25GR
      PRICE: 

      CAS Number
      343338-28-3
      Pack Size
      1GR, 5GR, 25GR
      Molecular Formula
      C4 H11 N O S
      Molecular Weight
      121.2
      MFCD
      05861480
      Storage Temp
      Refrigerator +4°C
      Brand
      Thermo Scientific - Alfa Aesar

      (S)-(-)-2-Methyl-2-propanesulfinamide is used in Suzuki reaction. It is also employed as a reagent for synthesizing chiral amines. It acts as a chiral auxiliary used in an asymmetric synthesis of trifluoroethylamines by conversion of trifluoroacetaldehyde to a chiral imine. It is also involved in the transformation of P,N-sulfinyl imine ligands through condensation with aldehydes and ketones, which can undergo iridium-catalyzed asymmetric hydrogenation of olefins. Further, it serves as a reagent for the preparation of chemicals and pharmaceutical intermediates.

      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
      (S)-(-)-2-Methyl-2-propanesulfinamide is used in Suzuki reaction. It is also employed as a reagent for synthesizing chiral amines. It acts as a chiral auxiliary used in an asymmetric synthesis of trifluoroethylamines by conversion of trifluoroacetaldehyde to a chiral imine. It is also involved in the transformation of P,N-sulfinyl imine ligands through condensation with aldehydes and ketones, which can undergo iridium-catalyzed asymmetric hydrogenation of olefins. Further, it serves as a reagent for the preparation of chemicals and pharmaceutical intermediates.

      Notes
      Incompatible with strong oxidizing agents. Store in a cool place.
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