Interesting facts
Interesting Facts about Acenaphthylene-1,2-dione
Acenaphthylene-1,2-dione, often regarded as a fascinating compound in the world of organic chemistry, possesses several intriguing characteristics that make it worthy of exploration:
- Structure and Reactivity: This compound features a unique framework, consisting of a bicyclic system. The arrangement of double bonds within its structure contributes to its reactivity, particularly in electrophilic aromatic substitution reactions.
- Fluorescence: Acenaphthylene-1,2-dione is noted for its *fluorescent properties*. When subjected to UV light, it can emit vibrant colors, making it valuable in various applications such as *fluorescent probes* in biological research.
- Applications: Beyond its role in academic research, this compound is utilized in the development of *dyes*, *pigments*, and *pharmaceuticals*. Its versatility stems from its ability to participate in various organic transformations.
- Polycyclic Aromatic Hydrocarbons (PAHs): Acenaphthylene-1,2-dione is often associated with PAHs, a class of compounds known for their significance in environmental studies due to their occurrence in fossil fuels and their potential health hazards.
- Historical Importance: This compound has contributed to the understanding of chemical reactivity and stability, promoting advancements in organic synthesis techniques that are fundamental to the field of synthetic chemistry.
In conclusion, Acenaphthylene-1,2-dione is not just an isolated molecule in the laboratory; it is a compound that bridges various fields of study—from environmental science to materials science, making it a significant subject of interest for chemists around the globe.
Synonyms
Acenaphthenequinone
82-86-0
acenaphthylene-1,2-dione
1,2-ACENAPHTHYLENEDIONE
Acenaphthoquinone
Acenaphthenedione
1,2-Acenaphthenequinone
1,2-Acenaphthenedione
Acenaphthaquinone
Acenaphthylenequinone
Acenaphthylene-1,2-quinone
acenaphthodione
diketoacenaphthene
1,2-Diketoacenaphthene
acenaphthylenedione
acenaphthene quinone
MFCD00003805
CCRIS 5318
acenaphthene-1,2-dione
CHEBI:15342
Acenaphthequinone
HSDB 2660
NSC 7656
EINECS 201-441-3
BRN 0879172
3950D6UEIQ
DTXSID7049429
NSC-7656
1,2-dihydroacenaphthylene-1,2-dione
DTXCID6029389
4-07-00-02498 (Beilstein Handbook Reference)
acenaphthenchinon
ACQ
UNII-3950D6UEIQ
acenaphtoquinone
acenaphtenquinone
1,2Acenaphthenequinone
1,2-Acenaphthalenedione
Acenaphthylene1,2quinone
acenaphthene-1,2-quinone
Epitope ID:116186
MLS000705880
SCHEMBL141538
1,2-dihydroacenaphthylenedione
CHEMBL395653
BDBM22853
NSC7656
1,2-Dione-Based Compound, 10
HMS2583D13
HMS3749K15
Tox21_202947
BBL011021
STK802161
AKOS000120366
CS-W017119
FA40598
CAS-82-86-0
NCGC00247177-01
NCGC00260493-01
AS-14620
BP-13440
SMR000225434
SY011135
DB-005405
A0004
NS00041019
EN300-20210
C02807
Q2739953
F1908-0136
Z104477294
InChI=1/C12H6O2/c13-11-8-5-1-3-7-4-2-6-9(10(7)8)12(11)14/h1-6
201-441-3
Solubility of Acenaphthylene-1,2-dione
Acenaphthylene-1,2-dione, a diketone compound, displays unique solubility characteristics that are characteristic of many aromatic compounds. When exploring its solubility properties, several important considerations come to light:
In summary, while acenaphthylene-1,2-dione is primarily soluble in nonpolar and mildly polar solvents, it is generally insoluble in water. This distinctive solubility behavior reflects the compound's hydrophobic characteristics and aromatic structure.