Interesting facts
Interesting Facts About 1,2,3-Trimethoxybenzene
1,2,3-Trimethoxybenzene, a fascinating aromatic compound, is part of a class known as methoxy-substituted benzenes. Its chemical structure is characterized by the presence of three methoxy groups (−OCH3) attached to a benzene ring at the 1, 2, and 3 positions.
Key Characteristics:
- Biological Significance: This compound exhibits potential biological activities, making it of interest in medicinal chemistry and pharmacology. Some studies suggest that methoxy-substituted benzenes may possess antioxidant properties.
- Synthetic Applications: 1,2,3-Trimethoxybenzene can be synthesized through various chemical reactions, including demethylation reactions of natural products, showcasing the versatility in synthetic organic chemistry.
- Industrial Uses: This compound serves as an essential intermediate in the synthesis of other complex molecules in organic chemistry, especially in dyes and fragrances.
Interestingly, the unique placement of methoxy groups on the benzene ring enhances the compound's chemical reactivity and stability, allowing it to participate in various chemical reactions that are fundamental in organic synthesis. As a student of chemistry, one might explore:
- How the electron-donating effect of the methoxy groups influences the compound's reactivity.
- The significance of regioselectivity in electrophilic aromatic substitution reactions involving 1,2,3-trimethoxybenzene.
- The exploration of its derivatives and their potential applications in advanced materials.
In conclusion, 1,2,3-trimethoxybenzene is not just a simple aromatic compound but a gateway to studying more complex organic reactions and their applications in various fields.
Synonyms
1,2,3-TRIMETHOXYBENZENE
Pyrogallol trimethyl ether
Tri-O-methylpyrogallol
Benzene, 1,2,3-trimethoxy-
Methylsyringol (VAN)
UNII-MRE1O894FG
MRE1O894FG
EINECS 211-207-2
NSC 10124
NSC-10124
AI3-02077
DTXSID1060899
CHEBI:86529
CRUILBNAQILVHZ-UHFFFAOYSA-
TriOmethylpyrogallol
Benzene, 1,2,3trimethoxy
DTXCID1043831
1,2,3-TMB
211-207-2
cruilbnaqilvhz-uhfffaoysa-n
inchi=1/c9h12o3/c1-10-7-5-4-6-8(11-2)9(7)12-3/h4-6h,1-3h3
methylsyringol
634-36-6
Trimethoxybenzene
1,2,3-trimethoxy benzene
MFCD00008358
1,2,3-Trimethoxybenzen
Benzene, trimethoxy-
1,2,3-trimethoxy-benzene
1,3-Trimethoxybenzene
2,3,4-trimethoxybenzene
1.2.3-Trimethoxybenzene
3,4,5-Trimethoxybenzene
bmse010218
Cambridge id 5108143
SCHEMBL151213
1,2,3-Trimethoxybenzene, 98%
HMS1577E02
BCP33591
NSC10124
STK499049
AKOS000120025
CS-W017808
FT71382
HY-W017092
AS-12689
PD158341
SY036393
DB-003154
NS00009609
T1102
EN300-20240
D70961
AH-034/32464032
Pyrogallol trimethyl ether;Benzene, 1,2,3-trimethoxy-
Q27159216
F0001-1721
Z104477452
Solubility of 1,2,3-trimethoxybenzene
1,2,3-trimethoxybenzene, known for its intriguing chemistry, demonstrates noteworthy solubility characteristics. Generally, the solubility of organic compounds can be influenced by several factors. For this compound, we observe the following:
This limited solubility in polar solvents encourages intriguing reactions in organic synthesis, often making 1,2,3-trimethoxybenzene a valuable compound for various chemical applications.
In summary, while 1,2,3-trimethoxybenzene exhibits considerable compatibility with many organic solvents, it remains relatively insoluble in water, which is a common trait for most nonpolar aromatic compounds.