1-aminoanthraquinone-2-carboxaldehyde
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- Molecular formula
- C15H9NO3
- CAS Number
- 6373-28-0
- IUPAC Name
- 1-amino-9,10-dioxo-anthracene-2-carbaldehyde
- Molecular Weight
- 237.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4700g/cm3
- Synonyms
- 6363-87-7
Identification
Interesting facts
Interesting Facts about 1-amino-9,10-dioxo-anthracene-2-carbaldehyde
1-amino-9,10-dioxo-anthracene-2-carbaldehyde is a fascinating compound that holds significant interest in the fields of organic chemistry and materials science. Below are some noteworthy aspects of this compound:
- Structural Significance: This compound features a distinctive anthracene framework — a polycyclic aromatic hydrocarbon consisting of three fused benzene rings. The presence of the carbonyl (C=O) and amino (NH2) functional groups contributes to its reactivity and potential applications.
- Fluorescent Properties: Anthracene derivatives are known for their excellent fluorescent properties. As a result, 1-amino-9,10-dioxo-anthracene-2-carbaldehyde could be a candidate for use in organic light-emitting diodes (OLEDs) and other optoelectronic devices.
- Potential Applications: Beyond its optical properties, the compound may serve roles in dye-sensitized solar cells, organic photovoltaics, and as pigments due to its vibrant coloration.
- Biological Relevance: Compounds like this one, with functional groups such as the amino group, may exhibit biological activity, potentially leading to investigations into pharmaceutical applications.
- Synthesis Challenges: Synthesizing such complex organic structures often requires advanced techniques in organic synthesis. This complexity opens doors to creativity in the lab as chemists devise innovative methods to construct these molecules.
In conclusion, 1-amino-9,10-dioxo-anthracene-2-carbaldehyde is more than just a collection of atoms; it represents possibilities in science and technology. Its unique properties invite ongoing research, paving the way for future discoveries and advancements.