Atomfair 2-Acetamido-5-methylthiazole C6H8N2OS CAS 61996-32-5

2-Acetamido-5-methylthiazole (CAS No. 61996-32-5) is a high-purity organic compound with the molecular formula C6H8N2OS and IUPAC name N-(5-methyl-1,3-thiazol-2-yl)acetamide . This specialized chemical features a thiazole core substituted with an acetamide group at the 2-position and a methyl group at the 5-position, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Our product is rigorously tested to ensure ≥98% purity by HPLC, with controlled moisture content (<0.5%) and low heavy metal impurities (50 mg/mL).

Description

2-Acetamido-5-methylthiazole (CAS No. 61996-32-5) is a high-purity organic compound with the molecular formula C6H8N2OS and IUPAC name N-(5-methyl-1,3-thiazol-2-yl)acetamide. This specialized chemical features a thiazole core substituted with an acetamide group at the 2-position and a methyl group at the 5-position, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Our product is rigorously tested to ensure ≥98% purity by HPLC, with controlled moisture content (<0.5%) and low heavy metal impurities (50 mg/mL).

Properties

  • CAS Number: 61996-32-5
  • Complexity: 140
  • IUPAC Name: N-(5-methylthiazol-2-yl)acetamide
  • InChI: InChI=1S/C6H8N2OS/c1-4-3-7-6(10-4)8-5(2)9/h3H,1-2H3,(H,7,8,9)
  • InChI Key: VAAPKQNASNXGQY-UHFFFAOYSA-N
  • Exact Mass: 156.03573406
  • Molecular Formula: C6H8N2OS
  • Molecular Weight: 156.21
  • SMILES: CC1=CN=C(S1)NC(=O)C
  • Topological: 70.2
  • Monoisotopic Mass: 156.03573406
  • Synonyms: 2-Acetamido-5-methylthiazole, 61996-32-5, N-(5-Methylthiazol-2-yl)acetamide, N-(5-methyl-thiazol-2-yl)-acetamide, N-(5-methyl-1,3-thiazol-2-yl)acetamide, MFCD18801061, NSC170683, Acetamide, N-(5-methyl-2-thiazolyl)-, SCHEMBL2175131, SCHEMBL6474925, CHEMBL3770595, DTXSID20305403, AKOS008918774, NSC-170683, BS-29154, DB-342157, CS-0209959, G85894

Application

2-Acetamido-5-methylthiazole serves as a key building block in medicinal chemistry for the synthesis of thiazole-containing drug candidates, particularly in developing antimicrobial and anti-inflammatory agents. Researchers utilize this compound as a precursor for creating more complex heterocyclic systems with potential CNS activity. In agrochemical research, it finds application in developing novel fungicides and plant growth regulators due to its thiazole scaffold. The compound’s structural features make it valuable for structure-activity relationship (SAR) studies in drug discovery programs targeting enzyme inhibition.

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