Interesting facts
Interesting Facts about 2,3-Dimethoxynaphthalene-1,4-dione
2,3-Dimethoxynaphthalene-1,4-dione is an intriguing compound that belongs to a class of organic molecules known for their unique structural properties and biological activities. Here are some fascinating insights into this compound:
- Structure and Function: This compound features a naphthalene backbone, characterized by two fused benzene rings, which is a common structure in many natural products. The presence of two methoxy groups enhances its chemical reactivity and influences its solubility in organic solvents.
- Biological Relevance: Compounds similar to 2,3-dimethoxynaphthalene-1,4-dione have been studied for their potential medicinal properties, including antimicrobial and anticancer activities. This compound may serve as a scaffold for the development of new therapeutic agents.
- Applications in Research: This compound is often utilized in synthetic organic chemistry as an intermediate for producing more complex molecules. Researchers frequently explore its derivatives for enhanced activities or novel properties.
- Photochemical Properties: The unique structure of naphthalene-based compounds allows for interesting photochemical behavior. The ability to absorb light and undergo chemical changes makes it of interest in materials science and photonic applications.
- Historical Context: Naphthalene derivatives have a rich history in organic chemistry studies, having been isolated and described long before their full structures were understood. This highlights the evolving nature of chemical research and discovery.
As you dive deeper into the chemistry of 2,3-dimethoxynaphthalene-1,4-dione, consider its multifaceted nature and the myriad of possibilities it presents for future research and applications.
Synonyms
dmnq
6956-96-3
2,3-Dimethoxy-1,4-naphthoquinone
2,3-dimethoxynaphthalene-1,4-dione
NSC 69355
1,4-Naphthalenedione,2,3-dimethoxy-
1,4-Naphthalenedione, 2,3-dimethoxy-
2,3-Dimethoxynaphthoquinone
CHEBI:64215
MFW94A3JEK
2,3-dimethoxy-1,4-naphthalenedione
NSC-69355
CHEMBL402468
DTXSID8040935
2,3-DIMETHOXY-1,4-DIHYDRONAPHTHALENE-1,4-DIONE
2,3-DIMETHOXY-P-NAPHTHOQUINONE
DMNQ?
UNII-MFW94A3JEK
Lopac-D-5439
NCIOpen2_003296
Lopac0_000399
MLS002153320
SCHEMBL571557
2,3-Dimethoxynaphthoquinone #
DTXCID6020935
HMS3261O19
2,3-Dimethoxy[1,4]naphthoquinone
BCP31298
NSC69355
Tox21_500399
BDBM50504346
HB3876
MFCD00184331
s6563
STL564769
AKOS022506394
CCG-204492
LP00399
SDCCGSBI-0050385.P002
NCGC00015348-01
NCGC00015348-02
NCGC00015348-03
NCGC00015348-04
NCGC00015348-05
NCGC00015348-08
NCGC00093826-01
NCGC00093826-02
NCGC00261084-01
BS-17479
SMR001230733
DB-098280
HY-121026
CS-0079331
EU-0100399
D 5439
D81157
SR-01000075819
2,3-Dimethoxy-1,4-naphthoquinone, >=99%, solid
SR-01000075819-1
Q27133127
DiMeNQ;NSC 69355; NSC-69355; NSC69355;2,3-Dimethoxy-1,4-naphthoquinone
Solubility of 2,3-Dimethoxynaphthalene-1,4-dione (C12H10O4)
2,3-Dimethoxynaphthalene-1,4-dione, with its distinctive structure, shows interesting solubility characteristics that can be important for various applications in chemistry and industry. Understanding its solubility is crucial, particularly in organic solvents and water.
Solubility Characteristics:
In summary, while 2,3-dimethoxynaphthalene-1,4-dione finds limited solubility in water, it's a viable candidate for dissolution in various organic solvents. Researchers and chemists aiming to utilize this compound should consider the solvent selection based on the desired application.