Interesting facts
Intriguing Insights into Bis(3-chlorophenyl)diazene
Bis(3-chlorophenyl)diazene is a fascinating compound that belongs to the family of azo compounds, which are known for their vivid colors and complex structures. Here are some intriguing facts that highlight its significance:
- Structure and Stability: This compound features a diazene moiety, which is characterized by the presence of a nitrogen-nitrogen double bond. The chlorine substitutions on the phenyl rings enhance the stability and reactivity of the compound.
- Applications: Bis(3-chlorophenyl)diazene holds importance in multiple fields such as organic synthesis, dye production, and materials science. It is often utilized in the synthesis of other azo compounds due to the ease of introducing further functional groups.
- Color Properties: A key characteristic of azo compounds, including bis(3-chlorophenyl)diazene, is their ability to impart vibrant colors. This feature is notable in the formulation of dyes, pigments, and other coloring agents used in various industries.
- Research Relevance: In academic research, bis(3-chlorophenyl)diazene serves as an important model compound for studying the properties and reactions of diazene derivatives. Its reactivity can provide insights into mechanisms of chemical transformations.
In summary, bis(3-chlorophenyl)diazene is more than just a chemical compound; it represents a blend of structural interest and practical applications. As expressed by researchers: "The study of azo compounds opens doors to understanding the color chemistry and the potential development of new materials."
Synonyms
Diazene, bis(3-chlorophenyl)-
15426-14-9
3,3'-dichloroazobenzene
bis(3-chlorophenyl)diazene
1,2-bis(3-chlorophenyl)diazene
(E)-bis(3-chlorophenyl)diazene
(E)-1,2-Bis(3-chlorophenyl)diazene
106131-24-2
Bis-(3-chlorophenyl)-diazene
SCHEMBL7870699
SCHEMBL7870702
DTXSID5074006
SCHEMBL30102029
ZAUXEPYLONOZEK-FOCLMDBBSA-N
AKOS004910356
(E)-1,2-Bis(3-chlorophenyl)diazene #
Solubility of bis(3-chlorophenyl)diazene
Bis(3-chlorophenyl)diazene, with its unique structure, exhibits interesting solubility properties. This compound’s solubility can be influenced by several factors, including:
In general, bis(3-chlorophenyl)diazene tends to be more soluble in organic solvents such as ether or chloroform, while water solubility is quite limited. It is essential to consider these factors when predicting its behavior in various environments.
In conclusion, the solubility of bis(3-chlorophenyl)diazene is a complex interplay of molecular characteristics and external conditions, making it vital for researchers to understand its interactions in different solvents.