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ISOQUINOLINIUM COMPOUND

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Identification
Molecular formula
C13H20ClNO2
CAS number
23490-01-9
IUPAC name
6-ethoxy-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium;chloride
State
State

At room temperature, this compound exists in solid state.

Melting point (Celsius)
172.00
Melting point (Kelvin)
445.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
297.80g/mol
Molar mass
297.8000g/mol
Density
1.2000g/cm3
Appearence

This compound appears as a crystalline solid and is typically white or off-white in color, depending on the purity and specific form of the compound.

Comment on solubility

Solubility of 6-ethoxy-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium;chloride

The solubility of 6-ethoxy-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium;chloride is influenced by several factors due to its complex organic structure. Here are some key points to consider:

  • Polarity: As a quaternary ammonium compound, it generally exhibits high polarity, which often leads to increased solubility in polar solvents such as water.
  • Chloride Ion: The chloride (Cl-) component enhances the solubility in aqueous solutions, as it tends to dissociate and facilitates ion-solvent interactions.
  • Organic Solvents: The presence of ethoxy and methoxy groups may improve solubility in organic solvents. Compounds with similar structures often show good solubility in solvents like ethanol, methanol, and dimethyl sulfoxide (DMSO).
  • Temperature Dependence: The solubility may also increase with temperature. Higher temperatures often enhance the solubility of organic compounds in various solvents.

In summary, this compound's solubility is characterized by its polarity, the influence of its chloride ion, and its behavior in different solvents, making it adaptable yet complex. As with any compound, experimental measurement is essential to determine precise solubility values in specific solvents.

Interesting facts

6-Ethoxy-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium; chloride

This compound, a member of the tetrahydroisoquinoline family, exhibits fascinating properties that have captivated scientists and researchers alike. Known for its rich chemical structure, the presence of multiple ethoxy and methoxy substituents makes it a valuable compound in medicinal chemistry. Here are some intriguing aspects of this compound:

  • Pharmacological Potential: Compounds of this class are often studied for their bioactive properties. They may exhibit activities such as anti-inflammatory, analgesic, and perhaps even neuroprotective effects, making them interesting candidates for drug development.
  • Structural Diversity: The unique arrangements of the ethoxy and methoxy groups contribute to the compound's stability and reactivity. Such diversity allows for numerous derivatives to be synthesized, expanding the scope of their applications in various fields.
  • Research Applications: Scientists utilize this compound to explore isoquinoline derivatives that exhibit promising results in combating certain diseases. Its potential role in the synthesis of new therapeutic agents highlights its significance in advancing pharmaceutical discoveries.
  • Chloride Anion: The presence of the chloride ion enhances the compound’s solubility in polar solvents, facilitating easier handling and reactivity in laboratory experiments, thus making it a preferred choice for experimental chemists.

Furthermore, research surrounding compounds like 6-ethoxy-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium; chloride is not just academically interesting but also has potential impacts in real-world applications, particularly in drug design and synthesis. As we continue to explore the chemical cosmos, such compounds underscore the intricate relationship between structure and function in medicinal chemistry.

Synonyms
N-Methyl-6-ethoxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride
7356-73-2
NSC 33641
Isoquinoline, 6-ethoxy-1,2,3,4-tetrahydro-7-methoxy-2-methyl-, hydrochloride
ISOQUINOLINE, N-METHYL-6-ETHOXY-7-METHOXY-1,2,3,4-TETRAHYDRO-, HYDROCHLORIDE