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  • (R)-(+)-2-Methyl-2-propanesulfinamide, 98%, Thermo Scientific Chemicals

    H27724.03
    CAS Number: 196929-78-9See All CAS: 196929-78-9 In Stock

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      Pack Size
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      CAT NUM: H27724.03
      (R)-(+)-2-Methyl-2-propanesulfinamide, 98%, Thermo Scientific Chemicals
      Pack Size: 1GR
      PRICE: 
      CAT NUM: H27724.06
      (R)-(+)-2-Methyl-2-propanesulfinamide, 98%, Thermo Scientific Chemicals
      Pack Size: 5GR
      PRICE: 
      CAT NUM: H27724.14
      (R)-(+)-2-Methyl-2-propanesulfinamide, 98%, Thermo Scientific Chemicals
      Pack Size: 25GR
      PRICE: 

      CAS Number
      196929-78-9
      Pack Size
      1GR, 5GR, 25GR
      Molecular Formula
      C4 H11 N O S
      Molecular Weight
      121.2
      MFCD
      05861479
      Storage Temp
      Refrigerator +4°C
      Brand
      Thermo Scientific - Alfa Aesar

      (R)-(+)-2-Methyl-2-propanesulfinamide is a chiral ligand, which is used in pharmaceutical compositions. Further, it is used in the preparation of beta-chloro sulfinamides in the synthesis of chiral azridines. It is involved in the preparation of organocatalyst for enantioselective reduction of imines. It serves as a reagent for synthesizing chiral amines. In addition to this, it is converted into P,N-sulfinyl imine ligands through condensation with aldehydes and ketones which undergoes iridium-catalyzed asymmetric hydrogenation of olefins.

      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
      (R)-(+)-2-Methyl-2-propanesulfinamide is a chiral ligand, which is used in pharmaceutical compositions. Further, it is used in the preparation of beta-chloro sulfinamides in the synthesis of chiral azridines. It is involved in the preparation of organocatalyst for enantioselective reduction of imines. It serves as a reagent for synthesizing chiral amines. In addition to this, it is converted into P,N-sulfinyl imine ligands through condensation with aldehydes and ketones which undergoes iridium-catalyzed asymmetric hydrogenation of olefins.

      Solubility
      Soluble in chloroform, methanol, tetrahydrofuran, dichloromethane, dimethyl sulfoxide and most organic solvents.

      Notes
      Incompatible with strong oxidizing agents, strong acids and bases. Store in a cool place.
      Certifications
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