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  • (+)-Diethyl L-tartrate, 98%, Thermo Scientific Chemicals

    A10641.0B

      CAT NUM
      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: A10641.0B
      (+)-Diethyl L-tartrate, 98%, Thermo Scientific Chemicals
      Pack Size: 1000GR
      PRICE: 
      CAT NUM: A10641.22
      (+)-Diethyl L-tartrate, 98%, Thermo Scientific Chemicals
      Pack Size: 100GR
      PRICE: 
      CAT NUM: A10641.30
      (+)-Diethyl L-tartrate, 98%, Thermo Scientific Chemicals
      Pack Size: 250GR
      PRICE: 
      CAT NUM: A10641.36
      (+)-Diethyl L-tartrate, 98%, Thermo Scientific Chemicals
      Pack Size: 500GR
      PRICE: 

      CAS Number
      87-91-2
      Pack Size
      1000GR, 100GR, 250GR, 500GR
      Molecular Formula
      C8 H14 O6
      Molecular Weight
      206.19
      MFCD
      00009143
      Density
      1.205
      Flash Point
      93
      Storage Temp
      RT
      Brand
      Thermo Scientific - Alfa Aesar

      (+)-Diethyl L-tartrate is used as a chiral auxiliary in the Sharpless enantioselective epoxidation of allylic alcohols, for Sharpless-type enantioselective oxidation of sulfides to sulfoxides and as a chiral auxiliary in the enantioselective construction of cyclopropanes from allylic alcohols by an asymmetric Simmons-Smith reaction. It is also used as a chiral reagent in a host of chemical reactions, such as the synthesis of isoquinoline alkaloids and arundic acid, which has been used in acute ischemic stroke therapy.

      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
      (+)-Diethyl L-tartrate is used as a chiral auxiliary in the Sharpless enantioselective epoxidation of allylic alcohols, for Sharpless-type enantioselective oxidation of sulfides to sulfoxides and as a chiral auxiliary in the enantioselective construction of cyclopropanes from allylic alcohols by an asymmetric Simmons-Smith reaction. It is also used as a chiral reagent in a host of chemical reactions, such as the synthesis of isoquinoline alkaloids and arundic acid, which has been used in acute ischemic stroke therapy.

      Solubility
      Fully miscible in water.

      Notes
      Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
      Certifications
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