Interesting facts
Exploring (2,3-diacetoxyphenyl) acetate
(2,3-diacetoxyphenyl) acetate is a fascinating compound that holds considerable interest in both organic synthesis and medicinal chemistry. Here are some intriguing facts that highlight its significance:
- Synthesis: This compound can be synthesized via acetylation reactions, commonly involving phenolic compounds. Such methods are central to building complex organic molecules in various chemical laboratories.
- Applications: (2,3-diacetoxyphenyl) acetate is not merely a laboratory curiosity. It is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, emphasizing the importance of acylated compounds in medicinal chemistry.
- Biological Activity: Compounds with similar structures have displayed biological activities, making (2,3-diacetoxyphenyl) acetate intriguing for drug discovery and development.
- Structure-Activity Relationships: Investigating how structural modifications affect biological activity can provide insights that are invaluable to medicinal chemists. This compound exemplifies such principles through its functional groups.
- Research Opportunities: The unique combination of acetoxy groups offers opportunities for research into steric effects and electronic properties, prompting students and chemists alike to explore and understand the reactivity and interaction of the compound.
In conclusion, (2,3-diacetoxyphenyl) acetate is more than just a chemical formula; it is a doorway to understanding the complexities of organic compounds, their synthesis, and their roles in the realms of biology and medicine. As chemists continue to unravel the connections between structure and function, this compound remains a valuable subject for study and exploration.
Synonyms
Pyrogallol triacetate
525-52-0
1,2,3-Triacetoxybenzene
Acetpyrogall
Lenigallol
Pyracetol
Pyrogallol, triacetate
Triacetylpyrogallol
1,2,3-BENZENETRIOL, TRIACETATE
NSC 24068
1,2,3-Phenenyl triacetate
1,2,3-Benzenetriol, 1,2,3-triacetate
2,3-Bis(acetyloxy)phenyl acetate
UNII-4TMC1R26A5
4TMC1R26A5
EINECS 208-374-9
NSC-24068
AI3-03113
DTXSID10883422
PYROGALLOL TRIACETATE [MI]
1,2,3-TRIACETYLBENZENETRIOLATE
Pyrogallol, triacetate (8CI)
DTXCID101022953
208-374-9
aqgltpnhaavokn-uhfffaoysa-n
Benzene-1,2,3-triyl triacetate
(2,3-diacetyloxyphenyl) acetate
MFCD00017220
1,3-Benzenetriol, triacetate
Benzene-1,2,3-triyltriacetate
SCHEMBL5212814
HMS1718I07
NSC24068
AKOS001064238
FP70552
DB-052138
NS00042394
Pyrogallol triacetate;1,2,3-Triacetoxybenzene
SR-01000054286
SR-01000054286-1
Q27260473
Z56995298
Solubility of (2,3-diacetoxyphenyl) acetate
(2,3-diacetoxyphenyl) acetate, with its unique functional groups, displays interesting solubility characteristics. This compound is generally soluble in organic solvents, owing to its ester groups that facilitate interactions with non-polar molecules. However, its solubility can be influenced by various factors:
As a rule of thumb, "like dissolves like," meaning that (2,3-diacetoxyphenyl) acetate will perform well in environments where the solvent's characteristics align closely with its own. Therefore, proper solvent selection is crucial for achieving desired solubility outcomes when working with this compound.