Sulfoxide Chloride

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Identification

Molecular formula
C6H6ClNO
CAS Number
35333-71-0
IUPAC Name
1-chloro-2-(sulfinylamino)benzene
Molecular Weight
173.61g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3700g/cm3
Synonyms
1-chloro-2-(sulfinylamino)benzene
Interesting facts

Interesting Facts about 1-chloro-2-(sulfinylamino)benzene

1-chloro-2-(sulfinylamino)benzene, a unique member of the aromatic amine family, holds significant interest in both medicinal and synthetic chemistry. Here are some intriguing aspects of this compound:

  • Structure & Functionality: The presence of a sulfinyl (–SO) group and a chloro (–Cl) substituent on the benzene ring introduces a fascinating interplay of electronic effects that can influence the compound's reactivity and biological activity.
  • Potential Applications: Due to its structural features, this compound could be explored for potential pharmacological activities. Researchers often investigate such compounds for their role in developing new therapeutic agents, particularly in treating diseases linked to inflammation or microbial infections.
  • Synthetic Routes: The synthesis of 1-chloro-2-(sulfinylamino)benzene can be approached through various methods, including nucleophilic substitution reactions. Chemists may modify the starting materials and reaction conditions to optimize yield and purity.
  • Research Significance: Reading scientific literature may unveil how modifications of the sulfinylamino group affect the compound’s properties and interactions with biological targets, making it a potential lead compound for drug discovery.
  • Environmental Chemistry: As with many chlorinated compounds, the environmental implications of 1-chloro-2-(sulfinylamino)benzene are a point of interest. Understanding its degradation pathways and ecological impact is essential for responsible chemical usage.

In summary, 1-chloro-2-(sulfinylamino)benzene is more than just a chemical; it is a compound that presents opportunities for exploration and discovery across various fields, from pharmacology to environmental science.

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