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    2-Acetamido-5-mercapto-1

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      2-Acetamido-5-mercapto-1,3,4-thiadiazole

      SKU
      A0756

      Category: Building Blocks, Intermediates, Reagents

      Synonyms
      2-Acetylamino-5-mercapto-1,3,4-thiadiazole, AcAMT, N-(5-sulfanyl-1,3,4-thiadiazol-2-yl)acetamide, NSC97893, Acetazolamide Impurity C
      32873-56-6
      CAS-Number
      C4H5N3OS2
      Molecular Formula
      175.24
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥96% (HPLC)
      Appearance
      White to pale yellow solid
      Identity
      1H-NMR

      Properties

      Solvents
      Soluble in DMSO.
      Density
      ~1.6 g/cm3 (Predicted)
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      +4°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at +4°C.
      Hazard statements
      H302-H315-H319-H335
      Precautionary statements
      P261-P280-P301+P312-P302+P352-P305+P351+P338
      GHS Symbol
      GHS07
      Signal word
      Warning
      Transportation
      Not dangerous goods
      Description
      2-Acetamido-5-mercapto-1,3,4-thiadiazole coatings are designed to prevent corrosion of metal ions by forming a barrier on metallic surfaces. 2-Acetylamino-5-mercapto-1,3,4-thiadiazole has been used in coatings as corrosion inhibitor for zinc and copper. 2-Acetamido-5-mercapto-1,3,4-thiadiazole is a intermediate and impurity acetazolamide (carbonic anhydrase inhibitor) and has been used for synthesis in organic chemistry.
      Smiles
      CC(=O)NC1=NNC(=S)S1
      InChi Key
      DWSMAMSVZRCQMP-UHFFFAOYSA-N
      References
      (1) G. Almajan, et al., Bioorg. Med. Chem. Lett. 15, 2347 (2005) , (2) S. Talath & A.K. Gadad, Eur. J. Med. Chem. 41, 918 (2006) , (3) L. Valek & S. Martinez, Mat. Lett. 61, 148 (2007) , (4) A.W. Schuttelkopf, et al., Bioorg. Med. Chem. 18, 8334 (2010) , (5) S.A. Al-Jibori, et al., Polyhedron 44, 210 (2012) , (6) A.F. Szoke, et al., Int. J. Biol. Macromol. 142, 423 (2020)

      2-Acetamido-5-mercapto-1,3,4-thiadiazole coatings are designed to prevent corrosion of metal ions by forming a barrier on metallic surfaces. 2-Acetylamino-5-mercapto-1,3,4-thiadiazole has been used in coatings as corrosion inhibitor for zinc and copper. 2-Acetamido-5-mercapto-1,3,4-thiadiazole is a intermediate and impurity acetazolamide (carbonic anhydrase inhibitor) and has been used for synthesis in organic chemistry.

      SKU: A0756 Category: Building Blocks, Intermediates, Reagents
      • Additional information

      Additional information

      Synonyms

      2-Acetylamino-5-mercapto-1,3,4-thiadiazole, AcAMT, N-(5-sulfanyl-1,3,4-thiadiazol-2-yl)acetamide, NSC97893, Acetazolamide Impurity C

      Purity

      ≥96% (HPLC)

      Appearance

      White to pale yellow solid

      CAS-Number

      32873-56-6

      Molecular Formula

      C4H5N3OS2

      Molecular Weight

      175.24

      Identity

      1H-NMR

      Solvents

      Soluble in DMSO.

      Density

      ~1.6 g/cm3 (Predicted)

      Smiles

      CC(=O)NC1=NNC(=S)S1

      InChi Key

      DWSMAMSVZRCQMP-UHFFFAOYSA-N

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      +4°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at +4°C.

      Hazard statements

      H302-H315-H319-H335

      Precautionary statements

      P261-P280-P301+P312-P302+P352-P305+P351+P338

      GHS Symbol

      GHS07

      Signal word

      Warning

      Transportation

      Not dangerous goods

      References

      (1) G. Almajan, et al., Bioorg. Med. Chem. Lett. 15, 2347 (2005), (2) S. Talath & A.K. Gadad, Eur. J. Med. Chem. 41, 918 (2006), (3) L. Valek & S. Martinez, Mat. Lett. 61, 148 (2007), (4) A.W. Schuttelkopf, et al., Bioorg. Med. Chem. 18, 8334 (2010), (5) S.A. Al-Jibori, et al., Polyhedron 44, 210 (2012), (6) A.F. Szoke, et al., Int. J. Biol. Macromol. 142, 423 (2020)

      Quantity

      5 g, 25 g, Bulk

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