Interesting facts
Interesting Facts about bis(4-chlorophenyl)diazene
bis(4-chlorophenyl)diazene is a fascinating compound with several notable characteristics and applications:
- Structure and Bonding: This compound features a unique structure where two 4-chlorophenyl groups are attached to a diazene moiety. The presence of nitrogen atoms in the structure adds to the intriguing chemistry related to diazene and its derivatives.
- Electrophilic Reactions: The azobenzene structure (related to diazene) in bis(4-chlorophenyl)diazene is significant in many organic reactions. Its ability to undergo electrophilic substitution makes it a valuable compound in synthetic chemistry.
- Photochemical Properties: Being related to azobenzene compounds, bis(4-chlorophenyl)diazene can be photoresponsive. It can undergo reversible isomerization upon exposure to light, making it useful in photonic applications and smart materials.
- Use in Dyes and Pigments: The chlorophenyl groups provide excellent color and stability, making this compound an ideal candidate for dyes and pigments in various industries.
- Research Applications: Scientists often explore bis(4-chlorophenyl)diazene as a precursor for more complex organic compounds or as a model for studying the reaction mechanisms of diazene derivatives in material science.
In summary, bis(4-chlorophenyl)diazene is not just a simple organic compound; it offers a window into the world of organic synthesis, photochemical phenomena, and material innovation. Its unique properties and applications make it a topic of interest for both students and professionals in the field of chemistry.
Synonyms
1602-00-2
1,2-Bis(4-chlorophenyl)diazene
4,4'-DICHLOROAZOBENZENE
Diazene, bis(4-chlorophenyl)-
p,p'-Dichloroazobenzene
Azobenzene, 4,4'-dichloro-
Diazene, 1,2-bis(4-chlorophenyl)-
HSDB 2720
0TL0OEH9RX
NSC 59160
BRN 0745559
NSC-59160
DTXSID701305943
2-16-00-00013 (Beilstein Handbook Reference)
4,4'-DICHLOROAZOBENZENE [HSDB]
p,p'Dichloroazobenzene
Azobenzene, 4,4'dichloro
Diazene, bis(4chlorophenyl)
DTXCID701735916
Diazene, bis(4-chlorophenyl)-(9CI)
633-903-9
Bis-(4-chloro-phenyl)-diazene
bis(4-chlorophenyl)diazene
21650-51-1
(E)-bis(4-chlorophenyl)diazene
(E)-1,2-Bis(4-chlorophenyl)diazene
44DICHLOROAZOBENZENE
UNII-0TL0OEH9RX
bis(4-chlorophenyl)-diazene
Diazene, bis(4-chlorophenyl)-, (E)-
Azobenzene,4'-dichloro-
SCHEMBL3282366
YSZC3310
(E)-bis(4-chlorophenyl)-diazene
XHQLXCFUPJSGOE-FOCLMDBBSA-N
XHQLXCFUPJSGOE-UHFFFAOYSA-N
BAA60200
NSC59160
AKOS015995105
AKOS024333043
(E)-1,2-Bis(4-chlorophenyl)diazene #
BS-21614
DB-307663
G10484
Q27250852
Solubility of bis(4-chlorophenyl)diazene
bis(4-chlorophenyl)diazene, with its unique structure, exhibits interesting solubility characteristics. Understanding the solubility of this compound is crucial for various applications and chemical processes. Here are some key points regarding its solubility:
In summary, the solubility of bis(4-chlorophenyl)diazene can be characterized as follows:
This solubility behavior is essential for scientists and researchers working with bis(4-chlorophenyl)diazene in synthesis and analyses, as it impacts the feasibility of its usage in different chemical contexts.