S-ethylisothiourea hydrochloride

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Identification

Molecular formula
C3H9ClN2S
CAS Number
541-22-0
IUPAC Name
[N'-(2-sulfanylethyl)carbamimidoyl]ammonium;chloride
Molecular Weight
138.62g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2020g/cm3
Interesting facts

Interesting Facts about N'-(2-sulfanylethyl)carbamimidoyl Ammonium Chloride

N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride is a fascinating compound that showcases the unique intersection of sulfur chemistry and ammonium compounds. Here are some noteworthy aspects of this intriguing compound:

  • Sulfur's Role: The presence of the sulfanyl (thiol) group in this compound introduces specific chemical properties. Sulfur is renowned for its ability to form strong bonds with carbon, which significantly contributes to the compound's stability.
  • Biological Relevance: Compounds containing sulfanyl groups are often found in biological systems. They can play essential roles in enzymatic reactions, cellular signaling, and protecting cells from oxidative stress.
  • Versatile Applications: Due to its unique structure, N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride can have potential applications in medicinal chemistry, particularly in the development of new therapeutic agents that may inhibit specific biological pathways.
  • Ammonium Feature: The ammonium portion of this compound contributes to its possible solubility properties and reactivity, making it an interesting subject for investigations related to ion exchange and coordination chemistry.

As we explore this compound further, scientists may uncover new synthetic routes and potential uses in various fields such as pharmaceuticals, materials science, and biochemistry. With ongoing research, the understanding of compounds like N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride continues to evolve, opening doors to innovative solutions in science.

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