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2,2-Diethoxyethanethiol

Base Information Edit
  • Chemical Name:2,2-Diethoxyethanethiol
  • CAS No.:53608-94-9
  • Molecular Formula:C6H14O2S
  • Molecular Weight:150.242
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60449113
  • Wikidata:Q82268466
  • Mol file:53608-94-9.mol
2,2-Diethoxyethanethiol

Synonyms:2,2-diethoxyethanethiol;53608-94-9;2,2-diethoxy-ethanethiol;1,1-Diethoxyethane-2-thiol;2,2-diethoxy-ethane-thiol;(2,2-diethoxyethyl)sulfane;2,2-diethoxy-ethylmercaptan;HSCH2CH(OC2H5)2;2,2-diethoxyethane-1-thiol;SCHEMBL1032455;DTXSID60449113;GUTQTHVYODVCQP-UHFFFAOYSA-N;EN300-1739433

Suppliers and Price of 2,2-Diethoxyethanethiol
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
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Total 7 raw suppliers
Chemical Property of 2,2-Diethoxyethanethiol Edit
Chemical Property:
  • XLogP3:1.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:150.07145086
  • Heavy Atom Count:9
  • Complexity:53
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(CS)OCC
  • Use Description 2,2-Diethoxyethanethiol, a chemical compound, has several applications in various fields. In the realm of organic synthesis and chemical research, it serves as a valuable reagent for introducing ethoxy and thiol functional groups into organic molecules, allowing for the creation of complex organic compounds with tailored properties. This compound plays a pivotal role in the development of new chemical reactions and the synthesis of specialized chemicals for pharmaceuticals, agrochemicals, and materials. Additionally, in the field of analytical chemistry, it can be employed as a derivatization agent to improve the detectability of certain compounds in gas chromatography and mass spectrometry, aiding in chemical analysis and identification. Its versatile utility underscores its significance in advancing organic chemistry, materials science, and analytical techniques, where it plays a crucial role in compound synthesis, materials development, and chemical analysis.
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