Interesting facts
Interesting Facts About 1-(2,4-Dihydroxyphenyl)ethanone
1-(2,4-Dihydroxyphenyl)ethanone, commonly known in the realm of organic chemistry, boasts a variety of intriguing characteristics and applications that make it worthy of study. Here are some key points:
- Natural Occurrence: This compound can be found in various natural sources, particularly in plants, where it may contribute to the complex profiles of phytochemicals.
- Antioxidant Properties: Studies have indicated that 1-(2,4-dihydroxyphenyl)ethanone exhibits significant antioxidant activity, which is essential for protecting biological systems from oxidative stress and damage.
- Chemical Versatility: The presence of two hydroxyl groups in its structure allows for extensive reactions, making it an excellent candidate for further chemical modifications and synthesis of diverse derivatives.
- Relevance in Pharmaceuticals: Due to its unique properties, this compound has gained interest in the pharmaceutical industry where it may be explored for its potential photoprotective effects and as a lead compound in drug discovery.
- Research Applications: Scientists are investigating the role of this compound in various biochemical pathways, particularly in relation to its effects on cell signaling and metabolism.
As one delves deeper into the realm of 1-(2,4-dihydroxyphenyl)ethanone, it becomes apparent that its multifaceted nature not only renders it significant for academic research but also highlights its potential impact across various fields, including nutrition, health, and pharmaceuticals.
In the words of a prominent chemist: "The true beauty of a compound like 1-(2,4-dihydroxyphenyl)ethanone lies not just in its structure, but in the possibilities it presents for innovation and discovery."
Synonyms
2',4'-DIHYDROXYACETOPHENONE
89-84-9
2,4-Dihydroxyacetophenone
1-(2,4-Dihydroxyphenyl)ethanone
Resacetophenone
4-Acetylresorcinol
Resoacetophenone
Ethanone, 1-(2,4-dihydroxyphenyl)-
1-Acetyl-2,4-dihydroxybenzene
Resorcinol, 4-acetyl-
MFCD00002279
Acetophenone, 2',4'-dihydroxy-
NSC 10883
1-(2,4-dihydroxyphenyl)ethan-1-one
UNII-UC3V356VZC
1-(2,4-dihydroxy-phenyl)-ethanone
EINECS 201-945-3
UC3V356VZC
BRN 1282505
CHEBI:18414
.beta.-Resacetophenone
AI3-00866
NSC-10883
4-Acetyl-1,3-benzenediol
2,4-Dihydroxy Acetophenone
2',4'-Dihydroxy-acetophenone
CHEMBL243374
4-08-00-01792 (Beilstein Handbook Reference)
WLN: QR CQ DV1
beta-Resacetophenone
4-Acetyl-Resorcinol
2,4-dihyroxyacetophenone
2,4-dihydroxy actophenone
2'4'-dihydroxyacetophenone
2,4,-dihydroxyacetophenone
1-Acetylbenzene-2,4-diol
RESACETOPHENONE [MI]
SCHEMBL26357
BIDD:ER0659
acetophenone, 2,4-dihydroxy-
1,3-Dihydroxy-4-acetylbenzene
2'',4''-dihydroxyacetophenone
2\',4\'-dihydroxyacetophenone
DTXSID4058998
1-(2,4-Dihydroxyphenyl)-ethanone
HY-Y0694
NSC10883
NSC37559
STR03384
2',4'-Dihydroxyacetophenone, 99%
BBL012128
BDBM50241221
NSC-37559
s4762
STK084318
AKOS000119522
AC-1105
CCG-259076
CS-W008599
FD22096
FS-3456
1-(2,4-Dihydroxyphenyl)ethanone, 9CI
SY004020
D0561
NS00039344
EN300-18418
C03663
S12324
AK-087/40177797
Q27103063
Z57101026
F1995-0239
1-(2,4-Dihydroxyphenyl)ethanone;1-Acetylbenzene-2,4-diol;Resacetophenone
2 inverted exclamation mark ,4 inverted exclamation mark -Dihydroxyacetophenone
InChI=1/C8H8O3/c1-5(9)7-3-2-6(10)4-8(7)11/h2-4,10-11H,1H
201-945-3
Solubility of 1-(2,4-Dihydroxyphenyl)ethanone
1-(2,4-Dihydroxyphenyl)ethanone, also known as acetovanillone, exhibits interesting solubility characteristics that are important for various applications. Understanding its solubility can help in determining the optimal conditions for its use in chemical processes and formulations.
Key Solubility Insights:
In summary, the solubility of 1-(2,4-dihydroxyphenyl)ethanone is a critical factor influenced by the nature of the solvent and environmental conditions. Among the factors that determine its effective use in chemical applications are the type of solvent, temperature, and pH. As such, “solubility is key” to ensuring that this compound can be utilized effectively in various scientific and industrial contexts.