Cysteamine hydrochloride
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- 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
Identification
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.