N-methylpyridine-2-thione-1-oxide sodium salt

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Identification

Molecular formula
C6H4NOSNa
CAS Number
15922-78-8
IUPAC Name
sodium;1-oxidopyridin-1-ium-2-thiolate
Molecular Weight
165.19g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4300g/cm3
Synonyms
sodium, 1-oxidopyridin-1-ium-2-thiolate
Interesting facts

Interesting Facts about Sodium 1-Oxidopyridin-1-ium-2-thiolate

Sodium 1-oxidopyridin-1-ium-2-thiolate is a fascinating compound that showcases the intriguing chemistry of sulfur-containing organic compounds. Here are some noteworthy aspects:

  • Role in Organic Chemistry: This compound often acts as a nucleophilic reagent due to the presence of the thiolate (-S-) group, making it valuable in various synthetic pathways.
  • Application in Coordination Chemistry: Sodium 1-oxidopyridin-1-ium-2-thiolate can coordinate with transition metals, forming complexes that are important in catalysis and materials science.
  • Biological Relevance: Compounds containing thiol groups, like this one, are crucial in biological systems, often participating in enzymatic reactions and contributing to the structure of proteins through disulfide bonds.
  • Electrochemical Properties: The unique properties of this compound allow it to be utilized in various electrochemical applications, including sensors and batteries.
  • Research Interest: As a compound featuring both nitrogen and sulfur atoms, it is of great interest to researchers studying the effects of heteroatoms in organic compounds and their reactivity in different environments.

While Sodium 1-oxidopyridin-1-ium-2-thiolate may not be the most well-known compound, its ability to participate in versatile reactions makes it a valuable asset in the toolkit of any chemist or chemical researcher. Its combination of organic and inorganic characteristics exemplifies the *intricacies of modern chemistry*.

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