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  • Thiazole, 99%, Thermo Scientific Chemicals

    L09970.03

      CAT NUM
      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: L09970.03
      Thiazole, 99%, Thermo Scientific Chemicals
      Pack Size: 1GR
      PRICE: 
      CAT NUM: L09970.06
      Thiazole, 99%, Thermo Scientific Chemicals
      Pack Size: 5GR
      PRICE: 
      CAT NUM: L09970.14
      Thiazole, 99%, Thermo Scientific Chemicals
      Pack Size: 25GR
      PRICE: 

      CAS Number
      288-47-1
      Hazard Class
      3
      Pack Size
      1GR, 5GR, 25GR
      Molecular Formula
      C3 H3 N S
      Molecular Weight
      85.13
      MFCD
      00005315
      Density
      1.2
      UN Number
      1993
      Flash Point
      22
      Storage Temp
      RT
      Brand
      Thermo Scientific - Alfa Aesar

      Thiazole is used as a flavoring agent and in the preparation of dyes and rubber accelerators. It serves as a component of the vitamin thiamine (B1). It acts as a protected formyl group used in natural product synthesis. It reacts with alkyl lithium and Grignard’s reagent to prepare organometallic complexes. It is involved in the electrophilic aromatic substitution and nucleophilic aromatic substitution at C-5 and C-2 positions respectively. Further, it undergoes alkylation reaction to get thiazolium cation, which is used as a catalyst in the Stetter reaction and the Benzoin condensation. In addition to this, it is involved in the preparation of alagebrium.

      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
      Thiazole is used as a flavoring agent and in the preparation of dyes and rubber accelerators. It serves as a component of the vitamin thiamine (B1). It acts as a protected formyl group used in natural product synthesis. It reacts with alkyl lithium and Grignard’s reagent to prepare organometallic complexes. It is involved in the electrophilic aromatic substitution and nucleophilic aromatic substitution at C-5 and C-2 positions respectively. Further, it undergoes alkylation reaction to get thiazolium cation, which is used as a catalyst in the Stetter reaction and the Benzoin condensation. In addition to this, it is involved in the preparation of alagebrium.

      Solubility
      Soluble in ethanol and ether. Slightly soluble in water.

      Notes
      Air and light sensitive. Incompatible with acids, acid chlorides, acid anhydrides, strong oxidizing agents and carbon dioxide.
      Certifications
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