Interesting facts
Interesting Facts about 3-benzoylchromen-2-one
3-benzoylchromen-2-one, a noteworthy compound in the realm of organic chemistry, is celebrated for its distinctive structure and diverse applications. Here are some engaging insights:
- Structural Significance: This compound features a chromenone structure, merging the aromatic properties of the benzoyl group with a chromene backbone. This unique arrangement allows for interesting chemical behavior and interactions.
- Biological Activities: Studies suggest that 3-benzoylchromen-2-one exhibits a range of biological activities. It has shown potential as an anti-inflammatory and antioxidant agent, making it a candidate for pharmaceutical exploration.
- Fluorescent Properties: The compound can exhibit fluorescence under certain conditions, which makes it useful in various fields such as **biochemistry** and **analytical chemistry**. Researchers often leverage this property for detection methods.
- Derivative Synthesis: Due to its reactive functional groups, 3-benzoylchromen-2-one serves as a versatile building block for synthesizing more complex organic compounds, such as derivatives that can enhance its biological activities.
- Natural Occurrence: Similar structures to 3-benzoylchromen-2-one can be found in several natural products, where they play roles in plant defense mechanisms and secondary metabolite production.
In summary, 3-benzoylchromen-2-one showcases a balance of structural complexity and functional diversity, making it a rich subject for research in organic and medicinal chemistry. As scholars and scientists delve deeper into its properties, the full potential of this compound continues to unfold.
Synonyms
3-Benzoylcoumarin
COUMARIN, 3-BENZOYL-
2H-1-Benzopyran-2-one, 3-benzoyl-
3-Benzoyl-2H-1-benzopyran-2-one
XF9P5UO8IN
NSC 11862
BRN 0190875
UNII-XF9P5UO8IN
NSC-11862
DTXSID6075144
5-17-11-00557 (Beilstein Handbook Reference)
DTXCID1035866
2H-1-Benzopyran-2-one, 3-benzoyl-(9CI)
1846-74-8
3-benzoyl-2H-chromen-2-one
3-benzoylchromen-2-one
3-Benzoyl-chromen-2-one
NSC11862
ChemDiv3_012376
Oprea1_857667
SCHEMBL51507
MLS001201222
CHEMBL591522
HMS1508C12
HMS2850G06
BAA84674
MFCD00233579
STL145336
3-(phenylcarbonyl)-2H-chromen-2-one
AKOS002087789
NCGC00245922-01
SMR000564143
DB-365952
CS-0359755
EU-0027162
SR-01000143218
SR-01000143218-1
BRD-K16706387-001-01-0
F0916-3926
Solubility of 3-benzoylchromen-2-one
3-benzoylchromen-2-one, known for its fascinating chemical structure, exhibits a variable solubility profile depending on the solvent used. This unique compound is generally characterized by:
In conclusion, the solubility of 3-benzoylchromen-2-one can be summarized as follows: it is primarily soluble in non-polar and medium polar solvents, while exhibiting limited solubility in polar solvents like water. Understanding these solubility characteristics is crucial for its application in various chemical and pharmaceutical processes.