Interesting facts
Interesting Facts about Bis(1-naphthyl)diazene
Bis(1-naphthyl)diazene, a fascinating azo compound, has garnered attention in the fields of organic chemistry and materials science. Here are some key points that highlight its significance:
- Structure & Stability: The compound features a distinctive structure where two 1-naphthyl groups are connected by a diazene (-N=N-) linkage. This unique arrangement contributes to its stability and reactivity in various chemical processes.
- Color and Photochemical Properties: As an azo compound, bis(1-naphthyl)diazene often displays vivid colors. These properties make it valuable in dyes and pigments, as well as in photochemical applications.
- Reactivity: The diazene group can act as a source of nitrogen-centered radicals, making bis(1-naphthyl)diazene a useful reagent in synthetic organic chemistry. Its ability to undergo various transformations allows chemists to explore new pathways in reaction mechanisms.
- Applications in Research: This compound is a subject of interest in studies related to materials such as polymer science, where it may be used to create specialized materials with desired optical and electronic properties.
- Biological Relevance: Azo compounds, like bis(1-naphthyl)diazene, have been investigated for their interactions with biological systems, including potential roles in drug delivery and therapeutic applications.
As noted by chemists, “The versatility of azo compounds makes them indispensable tools in both synthesis and application.” This reflects the broader significance of bis(1-naphthyl)diazene in advancing our understanding of chemical reactivity and application in practical fields.
In summary, bis(1-naphthyl)diazene stands out as a remarkable compound, offering numerous pathways for exploration and innovation in chemistry.
Synonyms
1,1'-AZONAPHTHALENE
487-10-5
Azonaphthalene
Diazene, di-1-naphthalenyl-
dinaphthalen-1-yldiazene
1,1'-Azobisnaphthalene
Di-1-naphthyldiazene
EINECS 207-648-5
di-naphthalen-1-yl-diazene
NSC 113051
BRN 0959427
NSC113051
Di(naphthalen-1-yl)diazene
SCHEMBL2291745
1,1'-Azonaphthalene - 80%
DTXSID50870553
1,2-Di(naphthalen-1-yl)diazene
DTXSID801032331
WLN: L66J BNUN- BL66J
(E)-1,2-Di(1-naphthyl)diazene #
AKOS024331732
FA70913
NSC-113051
DB-051576
NS00042839
Solubility of bis(1-naphthyl)diazene
bis(1-naphthyl)diazene, with its chemical structure containing both diazene and naphthalene rings, exhibits interesting solubility characteristics. Generally, the solubility of this compound can be influenced by several factors:
In conclusion, if you are working with bis(1-naphthyl)diazene, it's crucial to use the correct solvent to maximize its solubility, keeping in mind its predominantly non-polar nature. Testing in various organic solvents can yield the best results for experiments requiring the compound in solution.