Cysteamine hydrochloride

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Identification

Molecular formula
C2H8N2S · HBr
CAS Number
300-84-5
IUPAC Name
[N'-(2-sulfanylethyl)carbamimidoyl]ammonium;bromide
Molecular Weight
127.59g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.8000g/cm3
Interesting facts

Interesting Facts about N'-(2-sulfanylethyl)carbamimidoyl;ammonium; bromide

This intriguing compound, commonly known as a thiourea derivative, showcases remarkable properties and applications in various fields of chemistry. Here are some fascinating insights:

  • Unique Structure: The compound features a sulfenyl group that contributes to its reactivity, making it an interesting candidate for organic synthesis and medicinal chemistry.
  • Versatile Applications: It has been explored in the development of pharmaceuticals, agricultural chemicals, and catalytic processes, demonstrating its versatility in real-world applications.
  • Biological Relevance: Derivatives of thiourea compounds, including this one, have shown potential in biological systems, with studies indicating possible benefits in controlling metabolic pathways.
  • Reactivity: The compound can participate in various chemical reactions, including nucleophilic substitution and condensation reactions, highlighting its potential in synthetic organic chemistry.
  • Research Opportunities: Ongoing research continues to unveil new insights about the interactions and applications of this compound, emphasizing the need for exploration in both academic and industrial settings.

In summary, N'-(2-sulfanylethyl)carbamimidoyl;ammonium; bromide stands as a testament to the creativity and complexity found in chemical substances. As scientists continue to investigate its properties and potential, this compound could lead to exciting advancements in multiple scientific domains.

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