Chlorphenamide
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- Molecular formula
- C8H10ClNS2
- CAS Number
- 63993-05-7
- IUPAC Name
- 2-[(2-chlorophenyl)disulfanyl]ethanamine
- Molecular Weight
- 235.75g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4079g/cm3
Identification
Interesting facts
Exploring 2-[(2-chlorophenyl)disulfanyl]ethanamine
2-[(2-chlorophenyl)disulfanyl]ethanamine, a compound with intriguing structural characteristics, raises interest in both medicinal chemistry and synthetic applications. Here are some notable facts to consider:
- Structural Significance: The presence of the disulfanyl (āSāSā) moiety in its structure plays a crucial role in the compound's reactivity and stability, influencing how it interacts with various biological targets.
- Chlorophenyl Group: The chlorine atom on the phenyl ring can enhance the compound's electrophilicity, making it a potential candidate for further medicinal modifications aimed at enhancing therapeutic efficacy.
- Potential Applications: Research suggests that compounds featuring disulfide bonds may exhibit antioxidant properties, which are valuable in developing treatments for oxidative stress-related diseases.
- Biological Interest: With growing interest in compounds that target specific cellular pathways, the unique attributes of 2-[(2-chlorophenyl)disulfanyl]ethanamine may lend to investigations in cancer and other conditions where protein folding and stability are compromised.
- Synthetic Pathways: This compound can be synthesized through various methods, including nucleophilic substitution reactions followed by disulfide bond formation, highlighting the versatility of sulfur chemistry in creating complex organic molecules.
Overall, the investigation into 2-[(2-chlorophenyl)disulfanyl]ethanamine not only showcases the complexities of synthetic organic chemistry but also hints at its potential utility in the realm of pharmaceuticals.