Interesting facts
Interesting Facts about N-(1,4-dioxo-2-naphthyl)benzamide
N-(1,4-dioxo-2-naphthyl)benzamide is a remarkable compound known for its unique structural attributes and diverse applications in the field of chemistry. Here are some engaging insights:
- Functional Versatility: This compound exhibits dual functional groups, which contribute to its reactivity and interaction with biological systems. The naphthalene moiety provides an aromatic character that is valuable in various chemical reactions.
- Pharmaceutical Potential: Compounds similar to N-(1,4-dioxo-2-naphthyl)benzamide are often explored in drug discovery, particularly for their potential in fighting diseases due to their ability to interact with specific biological targets.
- Research Interest: Its intriguing molecular structure has drawn the attention of chemists, prompting extensive studies into its synthesis and reactivity, paving the way for novel applications in material science and organic synthesis.
- Photophysical Properties: The presence of the dioxo group enhances the compound’s photophysical characteristics, making it interesting for applications in photodynamic therapy and fluorescence-based technologies.
- Synthesis Challenge: The synthesis of this compound can be complex, often requiring intricate methods to ensure the desired functional groups are correctly incorporated, showcasing the challenges of organic synthesis.
- Potential Toxicity: Like many organic compounds, safety considerations are paramount. Some derivatives may exhibit toxicity, highlighting the need for careful handling and study during experimental applications.
In summary, N-(1,4-dioxo-2-naphthyl)benzamide stands as a noteworthy example of how intricate organic compounds can possess significant implications across various scientific fields, particularly in medicinal chemistry and organic synthesis.
Synonyms
ppm-18
65240-86-0
NQN-1
n-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)benzamide
N-(1,4-dioxonaphthalen-2-yl)benzamide
2-Benzoylamino-1,4-naphthoquinone
2-Benzamido-1,4-naphthoquinone
MLS002693850
2-Benzamido- 1,4-naphthoquinone
SMR001559791
NSC 73233
N-(1,4-Dihydro-1,4-dioxo-2-naphthalenyl)benzamide; N-(1,4-Dioxo-1,4-dihydronaphthalen-2-yl)benzamide; NSC 73233; PPM 18
NSC73233
N-(1,4-dihydro-1,4-dioxo-2-naphthalenyl)-benzamide
cid_4882
NCIOpen2_004005
SCHEMBL170388
GTPL7058
CHEMBL1717890
BDBM80067
DTXSID80274449
CHEBI:185746
GLXC-02763
HMS3085F17
EX-A9502
HSCI1_000119
NSC-73233
N-(1,4-diketo-2-naphthyl)benzamide
AKOS027422618
N-(1,4-dioxo-2-naphthalenyl)benzamide
DB-338103
HY-118160
CS-0065340
SR-01000880847
N-[1,4-bis(oxidanylidene)naphthalen-2-yl]benzamide
SR-01000880847-2
Q27088039
Solubility of N-(1,4-dioxo-2-naphthyl)benzamide
N-(1,4-dioxo-2-naphthyl)benzamide, with the molecular formula C17H11NO3, exhibits interesting solubility characteristics that are influenced by its molecular structure. The presence of both aromatic rings and a carbonyl functional group plays a crucial role in its solubility profile.
Key factors affecting the solubility include:
Given these factors, the potential solubility of N-(1,4-dioxo-2-naphthyl)benzamide is generally better in polar organic solvents such as Methanol and Ethanol, while it may be less soluble in nonpolar solvents like Hexane.
To summarize, one could state that the solubility of N-(1,4-dioxo-2-naphthyl)benzamide is dictated by a delicate balance of its complex structure, where intermolecular interactions and the chemical environment play a significant role in determining how well it dissolves in various solvents.