Interesting facts
Interesting Facts About 1,4-bis(2-hydroxyethylamino)anthracene-9,10-dione
This fascinating compound belongs to a class of organic molecules known as anthraquinones, which are known for their vibrant colors and intriguing chemical properties. Here are some engaging aspects of 1,4-bis(2-hydroxyethylamino)anthracene-9,10-dione:
- Biological Significance: Compounds like this one can exhibit biological activity, often being explored for their potential in pharmaceutical applications. Their unique structure allows them to interact with various biochemical pathways.
- Dye Applications: Anthraquinone derivatives are commonly used as dyes and pigments due to their strong chromophores, leading to applications in textiles, inks, and coatings.
- Synthetic Pathway: The synthetic route to create this compound can involve multiple steps, often starting from simpler anthracene derivatives and proceeding through functionalization reactions.
- Rheological Properties: Studies into the rheological properties of such compounds can pave the way for advancements in material science, especially in the development of new polymer blends.
- Spectroscopy: Due to the presence of conjugated double bonds, 1,4-bis(2-hydroxyethylamino)anthracene-9,10-dione is an excellent candidate for spectroscopy studies, allowing scientists to explore its electronic transitions.
Researchers often express excitement about exploring the myriad applications of such compounds. As one scientist noted, “Each molecule tells a story about its formation and potential uses; it’s up to us to decipher it.” Through continuous investigation, compounds like this one have the potential to unlock new discoveries across various fields, including medicine, materials science, and environmental chemistry.
Synonyms
1,4-Bis[(2-hydroxyethyl)amino]anthraquinone
1,4-Bis((2-hydroxyethyl)amino)anthraquinone
9,10-Anthracenedione, 1,4-bis((2-hydroxyethyl)amino)-
1,4-Bis((2-hydroxyethyl)amino)-9,10-anthracenedione
9,10-Anthracenedione, 1,4-bis[(2-hydroxyethyl)amino]-
1,4-Bis[(2-hydroxyethyl)amino]-9,10-anthracenedione
4471-41-4
Acetoquinone Blue BF
disperse blue 23
Nyloquinone Blue NP
Celliton Fast Blue BF
Serisol Brilliant Blue 2B
C.I. DISPERSE BLUE 23
C.I. 61545
1,4-BIS((2-HYDROXYETHYL)AMINO)ANTHRACENE-9,10-DIONE
O4U31606RT
NSC-128428
Anthraquinone, 1,4-bis((2-hydroxyethyl)amino)-
EINECS 224-743-7
1,4-bis[(2-hydroxyethyl)amino]anthracene-9,10-dione
NSC 128428
1,4-bis(2-hydroxyethylamino)anthracene-9,10-dione
BRN 2177770
UNII-O4U31606RT
CBMicro_026804
CI DISPERSE BLUE 23
1,4-Bis[(2-hydroxyethyl)amino]anthra-9,10-quinone
SCHEMBL1426702
CHEMBL2163808
DTXSID1063487
NSC128428
STL577125
AKOS037632638
9, 1,4-bis[(2-hydroxyethyl)amino]-
CI 61545
FB150718
1,4-bis(2-hydroxyethylamino)anthraquinone
BIM-0026681.P001
DB-259208
Anthraquinone,4-bis[(2-hydroxyethyl)amino]-
NS00021158
G67133
AB00091337-01
1,4-BIS(.BETA.-HYDROXYETHYLAMINO)ANTHRAQUINONE
Q27285333
5633-44-3
Solubility of 1,4-bis(2-hydroxyethylamino)anthracene-9,10-dione
The solubility of 1,4-bis(2-hydroxyethylamino)anthracene-9,10-dione can be influenced by several factors, including its chemical structure and the environment in which it resides. Here are key considerations regarding its solubility:
Given these factors, one could anticipate that 1,4-bis(2-hydroxyethylamino)anthracene-9,10-dione shows higher solubility in specific conditions. As a general rule, increased polarity and hydrogen bonding often lead to increased solubility. Thus, when considering solubility, it is crucial to assess both the solvent type and the molecular interactions at play.