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Isoquinoline a

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Identification
Molecular formula
C20H23Cl2NO4
CAS number
Not available
IUPAC name
1-[2-(3,4-dichlorophenyl)sulfonylethyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline
State
State

The compound is typically in a solid state at room temperature. It exists as a crystalline solid which is often white or off-white in appearance.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.20
Boiling point (Celsius)
440.40
Boiling point (Kelvin)
713.60
General information
Molecular weight
429.34g/mol
Molar mass
429.3370g/mol
Density
1.3622g/cm3
Appearence

The compound appears as a crystalline solid. It typically exhibits white or off-white coloration depending on its purity and any impurities that may be present. Notably, crystalline solids tend to reflect light, giving them a shiny appearance under direct illumination.

Comment on solubility

Solubility of 1-[2-(3,4-dichlorophenyl)sulfonylethyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline

The solubility of 1-[2-(3,4-dichlorophenyl)sulfonylethyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline is influenced by its unique chemical structure. Analyzing various factors can provide important insights:

  • Polar Functional Groups: The presence of sulfonyl and methoxy groups may enhance solubility in polar solvents.
  • Hydrophobic Regions: The dichlorophenyl component contributes to hydrophobic character, which could limit solubility in water.
  • Solvent Choice: This compound is likely more soluble in organic solvents, such as dimethyl sulfoxide (DMSO) or ethanol, compared to aqueous solutions.
  • Temperature Effects: Increasing the temperature can generally enhance the solubility of organic compounds.

In summary, the solubility of this compound can be described as preferentially enhanced in organic solvents due to both polar functional groups and hydrophobic regions. As a rule of thumb, compounds with substantial hydrophobicity often exhibit lower solubility in water, showcasing the classic "like dissolves like" principle in chemical solubility.

Interesting facts

Interesting Facts about 1-[2-(3,4-Dichlorophenyl)sulfonylethyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline

This compound, commonly referred to in the realm of medicinal chemistry, is noteworthy for its intricate structure and potential therapeutic applications. It belongs to a class of compounds known as isoquinoline derivatives, which are known for their diverse biological activities.

Chemical Properties and Structure

The unique features of this compound include:

  • Substituted Isoquinoline: The isoquinoline backbone offers a wide range of pharmacological properties, making it a scaffold of interest in drug discovery.
  • Dichlorophenyl Group: The presence of the 3,4-dichlorophenyl substituent enhances its potential as an antimicrobial or anti-cancer agent.
  • Sulfonamide Linkage: The sulfonamide group provides interesting interactions with biological targets, which may contribute to its potency.

Potential Applications

This compound has attracted attention for several reasons:

  • Pharmacological Activity: Compounds similar to this one have shown promise in treating various diseases, including cancers and bacterial infections.
  • Research Interest: Ongoing studies aim to explore its mechanisms of action, efficacy, and safety profile in clinical settings.
  • Framework for Drug Design: The structural complexity serves as a template for designing novel therapeutics with improved efficacy and selectivity.

Conclusion

In summary, 1-[2-(3,4-Dichlorophenyl)sulfonylethyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline is an intriguing compound that demonstrates the fascinating intersection between structural chemistry and medicinal applications. As more research unfolds, this compound may pave the way for breakthroughs in pharmaceuticals.