Interesting facts
Interesting Facts about 2-hydroxyanthracene-9,10-dione
2-hydroxyanthracene-9,10-dione, often referred to as flavanthrone, is a fascinating compound in the field of organic chemistry. Here are some intriguing aspects that highlight its significance:
- Structure and Stability: The compound features a fused ring structure that includes three fused benzene rings. This unique configuration contributes to its chemical stability and makes it an important subject of study in the field of polycyclic aromatic compounds.
- Fluorescent Properties: 2-hydroxyanthracene-9,10-dione exhibits notable fluorescent properties. It has been researched for potential applications in luminescent materials, which are central to modern technologies such as organic light-emitting diodes (OLEDs).
- Biological Activity: Research indicates that this compound may have biological relevance. Studies suggest potential antibacterial and antifungal activities, making it a candidate for further investigation in pharmaceutical applications.
- Environmental Impact: The compound is a derivative of anthracene, and as such, it garners attention for its environmental behaviors, particularly its role as a pollutant and its persistence in aquatic environments.
- Applications in Dye Chemistry: 2-hydroxyanthracene-9,10-dione is employed in dye chemistry, specifically as a dye intermediate. Its robust aromatic structure enables it to form various colorants used in textiles and other materials.
With its unique properties and potential applications across various fields, 2-hydroxyanthracene-9,10-dione remains an essential focus for chemists seeking to innovate and explore new frontiers in science. The blend of its structural complexity and functionality underscores the breadth of possibilities this compound presents.
Synonyms
2-HYDROXYANTHRAQUINONE
605-32-3
2-hydroxyanthracene-9,10-dione
2-Hydroxy-9,10-anthraquinone
Anthraquinone, 2-hydroxy-
9,10-Anthracenedione, 2-hydroxy-
beta-Hydroxyanthraquinone
2-Hydroxy-9,10-anthracenedione
CCRIS 9186
CHEBI:37482
.beta.-Hydroxyanthraquinone
NSC 2595
EINECS 210-085-8
2-Hydroxyanthra-9,10-quinone
DTXSID4049327
NSC-2595
2R8351U6Q0
DTXCID3029283
210-085-8
inchi=1/c14h8o3/c15-8-5-6-11-12(7-8)14(17)10-4-2-1-3-9(10)13(11)16/h1-7,15
MFCD00027374
27938-76-7
HYDROXY-9,10-ANTHRACENEDIONE
9, 2-hydroxy-
2-hydroxy-anthraquinone
SCHEMBL498619
CHEMBL446963
UNII-2R8351U6Q0
10-hydroxy-2,9-anthra-quinone
9,10-Anthracenedione,2-hydroxy
NSC2595
2-Hydroxyanthra-9,10-quinone #
2-hydroxyanthraquinone, AldrichCPR
BCP24349
Tox21_202901
BDBM50025601
AKOS001588311
CS-W013068
FH30762
HY-W012352
NCGC00260447-01
BS-17188
CAS-605-32-3
PD151278
SY051020
DB-053640
EU-0033611
H1012
NS00014408
D78173
Q27117163
2-Hydroxyanthraquinone (2-Hydroxy-9,10-anthracenedione)
Solubility of 2-hydroxyanthracene-9,10-dione
2-hydroxyanthracene-9,10-dione, also known as 1,4-dihydroxyanthraquinone, exhibits unique solubility characteristics that can be intriguing to study. Its solubility is influenced by several factors:
As a general observation, the solubility of 2-hydroxyanthracene-9,10-dione is a reflection of its chemical structure, with its effective interaction with solvents governed by polarity and hydrogen bonding. This compound's behavior in different environments makes it a subject of interest for further investigation and applications in various fields.