Skip to main content

1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium

ADVERTISEMENT
Identification
Molecular formula
C21H18NNaO5
CAS number
.
IUPAC name
1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium
State
State
At room temperature, this compound is typically a solid. Its crystallinity and structural integrity are stable at ambient conditions.
Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
343.37g/mol
Molar mass
343.3680g/mol
Density
1.2000g/cm3
Appearence
The compound is generally available as a crystalline solid. These crystals may appear as fine or elongated particles, and the color can range from off-white to pale yellow, depending on the purity and lighting conditions.
Comment on solubility

Solubility Overview of 1,2-Dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium

The solubility of the compound 1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium, with the chemical formula C21H18NNaO5, presents some intriguing characteristics due to its unique molecular structure.

Factors Influencing Solubility

Several factors can influence the solubility of this compound in various solvents:

  • Polarity of the Solvent: The presence of functional groups such as methoxy (-OCH3) and sodium (Na+) ions suggests that the compound may have higher solubility in polar solvents like water.
  • Hydrogen Bonding: The functional groups could facilitate hydrogen bonding, enhancing solubility in protic solvents.
  • Structural Geometry: The aromatic and heteroaromatic rings can impact how well the compound interacts with different solvents, affecting its overall solubility behavior.

Expected Solubility

It's reasonable to anticipate that:

  • 1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium may exhibit moderate to high solubility in aqueous solutions.
  • In non-polar solvents, the solubility would likely be quite low due to the compound's polar characteristics.

This solubility profile can be useful in various applications, from pharmaceuticals to materials science, allowing researchers to tailor solubility to the needs of their projects. Understanding the solubility dynamics of such compounds is crucial for optimizing their usage effectively.

Interesting facts

Interesting Facts about 1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium

1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium is a fascinating compound that offers insights into various fields, including organic chemistry and pharmacology. Here are some intriguing aspects of this compound:

  • Complex Structure: The compound features a unique fused ring system that integrates a benzodioxole and phenanthridine framework. This complex structure contributes to its interesting electronic properties and potential applications in materials science.
  • Potential Biological Activity: Compounds with similar structures have been studied for their biologically active properties, potentially including antimicrobial and anticancer activities. Researchers are keen to explore how the presence of methoxy groups and the cationic charge might enhance these activities.
  • Synthetic Relevance: The synthesis of compounds like this one is often a challenge for chemists, allowing them to develop and fine-tune methods for complex molecules. The study of its synthesis can lead to advancements in synthetic organic chemistry.
  • Stability of Ions: As a quaternary ammonium compound, it possesses a permanent positive charge, which may enhance its solubility and interaction with biological molecules, making it a point of interest in drug design.
  • Colorimetric Applications: The unique electronic configuration may allow the compound to be used in colorimetric assays or as a dye, exploiting its ability to absorb light at specific wavelengths.

Intriguingly, some literature notes that "the merging of multiple aromatic systems enhances the compound's ability to participate in electron transfer processes," making it a candidate for further research. 

In conclusion, 1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium is not just a name—it represents a rich tapestry of chemical possibilities waiting to be explored. Its structural characteristics and potential applications invite chemists to delve deeper into its properties and behaviors.

Synonyms
chelerythrine
34316-15-9
Toddalin
cheleritrine
Toddaline
broussonpapyrine
[1,3]Benzodioxolo[5,6-c]phenanthridinium, 1,2-dimethoxy-12-methyl-
EINECS 251-930-0
1,2-dimethoxy-12-methyl-[1,3]benzodioxolo[5,6-c]phenanthridin-12-ium
UNII-E3B045W6X0
CHEBI:78373
E3B045W6X0
1,2-Dimethoxy-12-Methyl[1,3]benzodioxolo[5,6-C]phenanthridin-12-Ium
CHEMBL13045
1,2-Dimethoxy-12-methyl(1,3)benzodioxolo(5,6-c)phenanthridinium
1,2-Dimethoxy-12-methyl-[1,3]dioxolo[4',5':4,5]benzo[1,2-c]phenanthridin-12-ium
1,2-Dimethoxy-12-methyl[1,3]benzodioxolo[5,6-c]phenanthridinium
1,2-Dimethoxy-12-methyl-[1,3]dioxolo-[4',5':4,5]benzo[1,2-c]phenanthridin-12-ium
(1,3)BENZODIOXOLO(5,6-C)PHENANTHRIDINIUM, 1,2-DIMETHOXY-12-METHYL-
1,2-DIMETHOXY-12-METHYL(1,3)DIOXOLO)4',5':4,5)BENZO(1,2-C)PHENANTHRIDINIUM
NSC646662
1,2-Dimethoxy-N-methyl(1,3)benzodioxolo(5,6-c)phenanthridinium chloride
Chelerytherine
Chelerythrine?
SR-01000075750
1,2-dimethoxy-12-methyl(1,3)benzodioxolo(5,6-c)phenanthridin-12-ium
CTI
Toddaline;Broussonpapyrine
Lopac-C-2932
CHELERYTHRINE [MI]
Lopac0_000241
BSPBio_001558
SCHEMBL288915
CHELERYTHRINE [WHO-DD]
GTPL5953
MEGxp0_001953
BDBM25524
DTXSID20861211
HMS1791N20
HMS1989N20
HMS3402N20
BCP02912
HY-N2359
STL581484
AKOS028108433
CCG-204336
FC73805
NCGC00015225-01
NCGC00015225-02
NCGC00015225-03
NCGC00015225-04
NCGC00015225-05
NCGC00015225-06
NCGC00015225-07
NCGC00162102-01
NCGC00162102-02
NCGC00162102-03
NCGC00162102-04
NCGC00162102-05
NCI60_003349
NCI60_041672
1ST157280
DB-050176
CS-0022541
NS00089928
Q5089853
SR-01000075750-5
BRD-K87904882-001-02-3
1,2-Dimethoxy-12-methyl-12lambda~5~-[1,3]benzodioxolo[5,6-c]phenanthridine hydrochloride
17,18-dimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{14,19}]henicosa-1(13),2,4(8),9,11,14(19),15,17,20-nonaen-21-ium
17,18-dimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{14,19}]henicosa-1(13),2,4(8),9,11,14,16,18,20-nonaen-21-ium
251-930-0