Interesting facts
Interesting Facts About 3,5-Dimethoxyphenol
3,5-Dimethoxyphenol, also known as 2,6-dimethoxyphenol, is an intriguing compound that piques the interest of both chemists and those studying organic compounds. Here are some compelling aspects of this fascinating molecule:
- Structure and Reactivity: The compound features a phenolic structure with two methoxy groups attached at the 3 and 5 positions. This unique substitution pattern contributes to its distinct chemical reactivity, making it a valuable intermediate in organic synthesis.
- Biological Activity: Research indicates that 3,5-dimethoxyphenol may exhibit antioxidant properties, which are beneficial in combating oxidative stress in biological systems. Such activities open up avenues for potential applications in pharmaceuticals and health supplements.
- Use in Synthesis: In the field of organic chemistry, it serves as a versatile building block for the synthesis of various compounds, including agrochemicals and pharmaceuticals. Its methoxy groups can easily undergo transformations, enhancing its utility in complex organic synthesis.
- Natural Occurrence: This compound can also be found in certain natural sources, suggesting its relevance in botanical studies and its potential roles in plant metabolism.
- Flavor and Fragrance: Due to its pleasant aromatic profile, 3,5-dimethoxyphenol has been explored in the fragrance industry for its possible application in flavoring and scent formulations.
As stated by many chemists, "Understanding the intricacies of compounds like 3,5-dimethoxyphenol not only enriches our knowledge of organic chemistry but also paves the way for innovations in various fields." Each study of this compound deepens our appreciation for the interconnectedness of chemistry and its applications in real-world scenarios.
Synonyms
3,5-Dimethoxyphenol
500-99-2
Phenol, 3,5-dimethoxy-
Taxicatigenin
Phloroglucinol dimethyl ether
1-Hydroxy-3,5-dimethoxybenzene
23UXW8136A
EINECS 207-917-7
NSC 70955
NSC-70955
DTXSID7075426
phloroglucindimethylether
1,3-dimethoxy-5-hydroxybenzene
DTXCID3040772
Phenol, 3,5-dimethoxy-(8CI)
Phenol, 3,5-dimethoxy-(8CI)(9CI)
207-917-7
MFCD00008388
CHEBI:88715
3,5-dimethoxy phenol
UNII-23UXW8136A
Phenol,5-dimethoxy-
3,5-dimethoxy-phenol
3 pound not5-Dimethoxyphenol
3,5-Dimethoxyphenol, 99%
SCHEMBL233829
CHEMBL462989
HMS1715K12
NSC70955
STR06179
BBL101113
s6071
STL554909
XH0635
AKOS000121581
CS-W001117
FD37978
HY-W001117
1-3-5-TRIMETHOXYBENZENE_met001
AC-11324
SY035504
DB-022082
NS00032004
P0320
EN300-16614
F17066
Q27160623
Z56347218
F0001-1304
InChI=1/C8H10O3/c1-10-7-3-6(9)4-8(5-7)11-2/h3-5,9H,1-2H
Solubility of 3,5-Dimethoxyphenol
3,5-Dimethoxyphenol, with the chemical formula C9H12O3, exhibits interesting solubility characteristics that are significant for its applications in chemical synthesis and pharmaceutical formulations.
Generally, the solubility of 3,5-dimethoxyphenol can be described as follows:
This solubility profile makes 3,5-dimethoxyphenol useful in various chemical reactions, where organic solvents are preferred for dissolution. It can be summarized that:
Understanding the solubility characteristics of 3,5-dimethoxyphenol is critical for scientists in order to effectively utilize this compound in various chemical processes.