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Atomfair Ethanethiol, 2-(4-(m-tolyloxy)butyl)amino-, hydrogen sulfate (ester) WR 2941 C13H21NO4S2

Description Ethanethiol, 2-(4-(m-tolyloxy)butyl)amino-, hydrogen sulfate (ester) (CAS No. 2417-72-3) is a specialized organic compound with the molecular formula C13H21NO4S2. This compound, also known by its IUPAC name 1-methyl-3-[4-(2-sulfosulfanylethylamino)butoxy]benzene , features a unique molecular structure combining a tolyloxybutylamino group with a thiosulfate ester moiety. It is commonly referred to by synonyms such as WR 2941 and S-2-((4-(m-Tolyloxy)butyl)amino)ethyl thiosulfate . This high-purity chemical is ideal for research applications requiring precise sulfur-containing intermediates or bioactive molecule synthesis. Available in various quantities, it is supplied with comprehensive analytical data including HPLC, GC-MS, and NMR to ensure quality and consistency for laboratory use.

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Description

Description

Ethanethiol, 2-(4-(m-tolyloxy)butyl)amino-, hydrogen sulfate (ester) (CAS No. 2417-72-3) is a specialized organic compound with the molecular formula C13H21NO4S2. This compound, also known by its IUPAC name 1-methyl-3-[4-(2-sulfosulfanylethylamino)butoxy]benzene, features a unique molecular structure combining a tolyloxybutylamino group with a thiosulfate ester moiety. It is commonly referred to by synonyms such as WR 2941 and S-2-((4-(m-Tolyloxy)butyl)amino)ethyl thiosulfate. This high-purity chemical is ideal for research applications requiring precise sulfur-containing intermediates or bioactive molecule synthesis. Available in various quantities, it is supplied with comprehensive analytical data including HPLC, GC-MS, and NMR to ensure quality and consistency for laboratory use.

  • CAS No: 2417-72-3
  • Molecular Formula: C13H21NO4S2
  • Molecular Weight: 319.4
  • Exact Mass: 319.09120050
  • Monoisotopic Mass: 319.09120050
  • IUPAC Name: 1-methyl-3-[4-(2-sulfosulfanylethylamino)butoxy]benzene
  • SMILES: CC1=CC(=CC=C1)OCCCCNCCSS(=O)(=O)O
  • Synonyms: WR 2941, BRN 2144023, S-2-((4-(m-Tolyloxy)butyl)amino)ethyl thiosulfate, 21224-80-6, 2-((4-(m-Tolyloxy)butyl)amino)ethanethiol hydrogen sulfate (ester)

Application

This compound is primarily utilized as a biochemical intermediate in pharmaceutical and agrochemical research. Its unique thiosulfate ester structure makes it valuable for studying sulfur-based drug delivery systems or as a precursor in organosulfur chemistry. Researchers may also explore its potential in enzyme inhibition studies due to its reactive functional groups. Suitable for controlled laboratory environments, it requires proper handling due to its chemical reactivity.

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