Interesting facts
Interesting Facts about 1-(2,5-dihydroxyphenyl)ethanone
1-(2,5-dihydroxyphenyl)ethanone, commonly referred to in various studies for its unique chemical structure, showcases several intriguing characteristics:
- Biological Relevance: This compound is often studied for its potential biological activities. It can serve as a building block in the synthesis of more complex organic molecules, which may possess antioxidant and anti-inflammatory properties.
- Phenolic Structure: As a phenolic compound, it contains multiple hydroxyl groups attached to the benzene ring. This structure contributes to its reactivity and provides a site for various chemical transformations.
- Natural Occurrences: Compounds with similar structures can be found in various natural sources, particularly in plants, where they might play a role in defense mechanisms against pests and pathogens.
- Medicinal Chemistry: In the realm of medicinal chemistry, understanding such compounds can lead to the development of new therapeutic agents. Researchers are exploring its potential applications in pharmaceuticals.
- Research Applications: It is often used as a model compound in studies related to chemical reactivity and mechanism elucidation, allowing scientists to draw parallels with more complex biochemical processes.
In summary, the compound 1-(2,5-dihydroxyphenyl)ethanone presents a fascinating area of study within both organic and medicinal chemistry, reflecting the intricate relationship between molecular structure and biological function. As noted by chemists, “Every molecule tells a story; it’s up to us to decipher it.”
Synonyms
490-78-8
2',5'-DIHYDROXYACETOPHENONE
1-(2,5-Dihydroxyphenyl)ethanone
2-Acetylhydroquinone
Quinacetophenone
Acetylhydroquinone
Ethanone, 1-(2,5-dihydroxyphenyl)-
Acetylquinol
1-(2,5-dihydroxyphenyl)ethan-1-one
Acetophenone, 2',5'-dihydroxy-
1-Acetyl-2,5-dihydroxybenzene
NSC 3759
2,5-Dihydroxy-1-acetylbenzene
EINECS 207-716-4
K1H7QH11ZH
BRN 0637903
AI3-18221
NSC-3759
DTXSID9060077
2-ACETYL-1,4-BENZENEDIOL
4-08-00-01803 (Beilstein Handbook Reference)
DTXCID7040659
2-ACETYLHYDROQUINONE [INCI]
207-716-4
inchi=1/c8h8o3/c1-5(9)7-4-6(10)2-3-8(7)11/h2-4,10-11h,1h
2,5-Dihydroxyacetophenone
MFCD00002343
ghl.PD_Mitscher_leg0.355
2', 5'-Dihydroxyacetophenone
2-Acetyl-1,4-dihydroxybenzene
2,5-Dihydroxyphenyl methyl ketone
UNII-K1H7QH11ZH
NSC3759
2-acetyl hydroquinone
2-acetyl-hydroquinone
monoacetyl hydroquinone
2,5 -dihydroxyacetophenone
WLN: QR CQ BV1
2,5-Dihydroxy acetophenone
Acetophenone,5'-dihydroxy-
2`,5`-Dihydroxyacetophenone
Ethanone,5-dihydroxyphenyl)-
BIDD:ER0488
SCHEMBL108053
2',5'-Dihydroxy-Acetophenone
CHEMBL2348532
CHEBI:173647
1-(2,5-dihydroxyphenyl)-ethanone
ALBB-019961
STR02363
1-(2,5-dihydroxy-phenyl)-ethanone
2',5'-Dihydroxyacetophenone, 97%
BBL027378
s9374
STL199230
AKOS000120785
CCG-266221
CS-W001174
FD36336
FS-3211
HY-W001174
1-(2,5-Dihydroxyphenyl)ethanone, 9CI
s12309
AC-19701
SY011591
D1955
DHAP, 2-Acetylhydroquinone, Quinacetophenone
NS00031851
EN300-17127
AE-641/00693054
Q27281823
Z56889030
F3139-0239
2 inverted exclamation mark ,5 inverted exclamation mark -Dihydroxyacetophenone
Solubility of 1-(2,5-dihydroxyphenyl)ethanone
1-(2,5-dihydroxyphenyl)ethanone, commonly referred to as a derivative of flavonoids, exhibits interesting solubility properties that are worth noting:
In summary, the solubility characteristics of 1-(2,5-dihydroxyphenyl)ethanone emphasize its utility in various analytical and synthetic applications where solubility in polar media is advantageous. Its hydroxyl functionalities not only enhance its solubility but may also play a role in biological interactions, making it a compound of interest in both chemistry and pharmacology.