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Atomfair 2,3-Dichlorobenzenethiol C6H4Cl2S

Description 2,3-Dichlorobenzenethiol (CAS No. 17231-95-7) is a high-purity organosulfur compound with the molecular formula C6H4Cl2S , widely utilized in organic synthesis and pharmaceutical research. This aromatic thiol features two chlorine substituents at the 2- and 3-positions, enhancing its reactivity in nucleophilic substitution and metal-coupling reactions. Its precise molecular weight (179.07 g/mol) and low water solubility make it ideal for controlled reactions under anhydrous conditions. Packaged under inert gas to prevent oxidation, our ??98% pure product is rigorously tested via GC/MS and NMR to ensure consistency for sensitive applications. Suitable for use as a building block in agrochemicals, ligands, and heterocyclic…

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Description

Description

2,3-Dichlorobenzenethiol (CAS No. 17231-95-7) is a high-purity organosulfur compound with the molecular formula C6H4Cl2S, widely utilized in organic synthesis and pharmaceutical research. This aromatic thiol features two chlorine substituents at the 2- and 3-positions, enhancing its reactivity in nucleophilic substitution and metal-coupling reactions. Its precise molecular weight (179.07 g/mol) and low water solubility make it ideal for controlled reactions under anhydrous conditions. Packaged under inert gas to prevent oxidation, our ??98% pure product is rigorously tested via GC/MS and NMR to ensure consistency for sensitive applications. Suitable for use as a building block in agrochemicals, ligands, and heterocyclic frameworks.

  • CAS No: 17231-95-7
  • Molecular Formula: C6H4Cl2S
  • Molecular Weight: 179.07
  • Exact Mass: 177.9410767
  • Monoisotopic Mass: 177.9410767
  • IUPAC Name: 2,3-dichlorobenzenethiol
  • SMILES: C1=CC(=C(C(=C1)Cl)Cl)S
  • Synonyms: 2,3-Dichlorothiophenol, 17231-95-7, 2,3-Dichlorobenzenethiol, 43G4NGA9AN, QGRKONUHHGBHRB-UHFFFAOYSA-

Application

2,3-Dichlorobenzenethiol serves as a versatile intermediate in the synthesis of sulfur-containing pharmaceuticals and ligands for transition-metal catalysis. It is employed in the preparation of fungicides and herbicides due to its bioactive aromatic structure. Researchers also use it to modify polymer matrices or as a precursor for conductive materials in electronics.

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