Interesting facts
Interesting Facts about 1,4-Diimino-2,3-dihydroanthracene-9,10-diol
1,4-Diimino-2,3-dihydroanthracene-9,10-diol is a fascinating compound with numerous implications in both organic chemistry and materials science. Here are some engaging points that highlight its significance:
- Structural Composition: This compound features a unique anthracene backbone, augmented by diazene groups and hydroxyl functionalities, leading to interesting electronic properties. The presence of these functional groups can significantly influence its reactivity and interactions with other molecules.
- Potential Applications: The electron-rich nature of the double bonds and amine groups gives this compound potential in various applications such as:
- Organic Electronics: It may serve as a building block for conducting polymers.
- Photovoltaics: Its unique absorption properties could be harnessed in solar cell technology.
- Redox Properties: The imino groups (–NH) in 1,4-diimino-2,3-dihydroanthracene-9,10-diol can undergo oxidation and reduction reactions, making this compound a potential candidate for redox flow batteries.
- Biological Significance: Complex organic compounds like this can sometimes exhibit biological activity, suggesting that it may have potential in medicinal chemistry, particularly in the design of new pharmaceuticals.
- Synthesis Challenges: The synthesis of such multi-functional compounds often involves intricate organic reactions, showcasing the importance of mastering various methodologies in synthetic organic chemistry.
In conclusion, 1,4-diimino-2,3-dihydroanthracene-9,10-diol stands out not only for its structural elegance but also for its promising applications across various fields. Its balance of reactivity, electrochemical properties, and potential uses makes it a worthwhile subject of study for chemists and material scientists alike.
Synonyms
81-63-0
1,4-DIAMINO-2,3-DIHYDROANTHRAQUINONE
1,4-diamino-2,3-dihydroanthracene-9,10-dione
Solvent Violet 47
9,10-Anthracenedione, 1,4-diamino-2,3-dihydro-
C.I. Solvent Violet 47
NSC 23123
CCRIS 5607
Anthraquinone, 1,4-diamino-2,3-dihydro-
EINECS 201-367-1
BRN 2125631
U46FO9XL97
Anthraquinone, 2,3-dihydro-1,4-diamino-
NSC-23123
1,4-Diamino-2,3-dihydro-9,10-anthracenedione
MLS000738012
DTXSID70883261
1,4-Diimino-2,3-dihydroanthracene-9,10-diol
J192.590C
1,4-DIAMINO-2,3-DIHYDRO-9,10-ANTHRAQUINONE
UNII-U46FO9XL97
1,3-dihydroanthraquinone
SCHEMBL4800950
CHEMBL3392069
REGID_for_CID_663251
REGID_for_CID_5354979
SSGALQHXKMAJTL-UHFFFAOYSA-N
UFVDYITXJBCPMW-UHFFFAOYSA-N
DTXCID001022805
9, 1,4-diamino-2,3-dihydro-
NSC23123
AKOS015854642
Anthraquinone,4-diamino-2,3-dihydro-
SB80619
1,4-Diamino-2, 3-dihydroanthraquinone
1,4-Diamino-2,3-dihydro-anthraquinone
NCGC00246921-01
AS-14243
DB-056545
CS-0331014
NS00041174
D95746
Anthraquinone, 1,4-diamino-2,3-dihydro-(8CI)
1,4-Diamino-2,3-dihydro-9,10-anthracenedione #
Q4545694
1,4-Diamino-2,3-dihydro-9,10-anthraquinone;Solvent violet 47
201-367-1
Solubility of 1,4-Diimino-2,3-dihydroanthracene-9,10-diol
The solubility of 1,4-diimino-2,3-dihydroanthracene-9,10-diol can be influenced by various factors, including its molecular structure, the presence of functional groups, and the solvent in question. Here are key points to consider:
As a general observation, the solubility of 1,4-diimino-2,3-dihydroanthracene-9,10-diol is expected to be preferentially favorable in polar solvents, making tasks such as extraction and processing crucially dependent on the chosen solvent system. Experimentation may be essential to fully characterize its solubility behaviors.