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Tetramethoxy-isoquinolinoisoquinolinium

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Identification
Molecular formula
C22H22N2O4
CAS number
30697-78-6
IUPAC name
2,3,10,11-tetramethoxy-8-methyl-isoquinolino[2,1-b]isoquinolin-7-ium
State
State

At room temperature, this compound exists as a solid. The chemical structure contributes to its stability and firmness at ambient conditions.

Melting point (Celsius)
242.00
Melting point (Kelvin)
515.15
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.15
General information
Molecular weight
356.42g/mol
Molar mass
356.4200g/mol
Density
1.3200g/cm3
Appearence

The compound typically appears as a whitish to off-white powder. It is primarily obtained in crystalline form, exhibiting a fine texture. Due to the presence of methoxy groups, the crystals might appear slightly glossy.

Comment on solubility

Solubility of 2,3,10,11-tetramethoxy-8-methyl-isoquinolino[2,1-b]isoquinolin-7-ium

The solubility of 2,3,10,11-tetramethoxy-8-methyl-isoquinolino[2,1-b]isoquinolin-7-ium is a vital characteristic that affects its potential applications, interactions, and behavior in various environments.

This compound is often considered to have:

  • Low Water Solubility: Due to the presence of multiple methoxy groups, which can increase hydrophobic characteristics and reduce solubility in polar solvents.
  • Better Solubility in Organic Solvents: Such as ethanol, methanol, or acetone, making it more versatile for experimental conditions in organic chemistry.
  • pH-Dependent Solubility: The solubility can also vary with changes in pH, potentially affecting its ionic state and, in turn, its interactions with other substances.

As a general guideline, it is essential to remember that:

  1. Compounds like this often reach their solubility limits in organic solvents under specific conditions.
  2. The temperature of the solvent can significantly influence solubility; higher temperatures typically enhance solubility.
  3. Interactions with other solutes or solvents can lead to precipitation or complexation, affecting overall solubility.

Understanding the solubility of this compound will not only contribute to the development of new materials and applications but also aid in predicting its behavior in biological systems and environmental contexts. Further studies are essential to uncover the full solubility profile under a variety of conditions.

Interesting facts

Insights into 2,3,10,11-tetramethoxy-8-methyl-isoquinolino[2,1-b]isoquinolin-7-ium

The compound 2,3,10,11-tetramethoxy-8-methyl-isoquinolino[2,1-b]isoquinolin-7-ium is a fascinating member of the isoquinoline family, known for its complex structure and notable properties. Here are some intriguing aspects that highlight its significance in the realm of chemistry:

  • Diverse Applications: This compound has been studied for potential applications in various fields such as medicinal chemistry, where its unique properties might play a role in drug development.
  • Synthetic Pathways: The synthesis of this isoquinoline derivative showcases the complexity of organic reactions, often involving advanced methods in organic synthesis.
  • Bioactivity: Some studies suggest that compounds with similar structures exhibit interesting biological activities, including anticancer and antimicrobial properties, making this compound a potential candidate for further research.
  • Analytical Techniques: Investigating such compounds requires various sophisticated analytical methods, including NMR spectroscopy and mass spectrometry, to decipher their structural and functional aspects.
  • Research Frontiers: The incorporation of methoxy groups in its structure adds to the fascinating chemistry of isoquinolines, prompting further exploration into their electronic properties and reactivity.

As a scientist or a chemistry student, understanding compounds like 2,3,10,11-tetramethoxy-8-methyl-isoquinolino[2,1-b]isoquinolin-7-ium not only enriches our knowledge of organic chemistry but also opens up avenues for innovative research and discovery. The sandbox of organic compounds continues to surprise and inspire with each new exploration!

Synonyms
Coralyne sulfoacetate
2,3,10,11-tetramethoxy-8-methylisoquinolino[2,1-b]isoquinolin-7-ium
Monoanhydride with sulfuric acid
2,3,10,11-tetramethoxy-8-methylisoquino[3,2-a]isoquinolinium
NSC343342
1031265-39-0
38989-37-6
Spectrum_001122
SpecPlus_000603
Prestwick0_000431
Prestwick1_000431
Prestwick2_000431
Prestwick3_000431
Spectrum2_000605
Spectrum3_000718
Spectrum4_001865
Spectrum5_000430
NCIMech_000651
BSPBio_000442
BSPBio_002535
KBioGR_002332
KBioSS_001602
DivK1c_006699
SCHEMBL278878
SPBio_000510
SPBio_002381
BPBio1_000488
CHEMBL1184668
KBio1_001643
KBio2_001602
KBio2_004170
KBio2_006738
KBio3_001755
CHEBI:104157
DTXSID201319165
BBL036682
STL559061
AKOS037516171
SDCCGMLS-0066682.P001
2,3,10,11-Tetramethoxy-8-methylisoquino[3,2-a]isoquinolinium carboxymethanesulfonate
NCGC00178614-01
NCI60_001099
NCI60_042149
BRD-K24443173-311-03-7
Q27181476
2,3,10,11-tetramethoxy-8-methyl-isoquinolino[2,1-b]isoquinolin-7-ium
Dibenzo[a,g]quinolizinium, 2,3,10,11-tetramethoxy-8-methyl-, chloride, monohydrate