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1-Methyl-7-phenyl-3,4-dihydroisoquinoline

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Identification
Molecular formula
C16H15N
CAS number
105113-06-6
IUPAC name
1-methyl-7-phenyl-3,4-dihydroisoquinoline
State
State

Normally observed as a solid at room temperature.

Melting point (Celsius)
52.00
Melting point (Kelvin)
325.15
Boiling point (Celsius)
350.10
Boiling point (Kelvin)
623.25
General information
Molecular weight
219.31g/mol
Molar mass
219.3070g/mol
Density
1.0690g/cm3
Appearence

1-Methyl-7-phenyl-3,4-dihydroisoquinoline typically appears as a yellow or off-white crystalline solid. Its appearance may vary depending on the specific sample and purity.

Comment on solubility

Solubility of 1-methyl-7-phenyl-3,4-dihydroisoquinoline

The solubility of 1-methyl-7-phenyl-3,4-dihydroisoquinoline (C17H18N) is of great interest due to its structural characteristics which impact its interaction with solvents.

Generally, this compound is expected to exhibit:

  • Moderate solubility in organic solvents: This includes solvents like ethanol, methanol, and dichloromethane, where the non-polar phenyl ring enhances its interaction with non-polar or slightly polar solvents.
  • Poor solubility in water: Given its hydrophobic regions, 1-methyl-7-phenyl-3,4-dihydroisoquinoline is likely to have limited solubility in aqueous environments, resulting in low dissolution rates.

As a result, if one were to quote the general rule, "like dissolves like," this compound's behavior reflects its structure. The intricate balance between hydrophilic and hydrophobic parts influences solubility, which is crucial for applications in organic synthesis and pharmaceuticals.

In sum, understanding the solubility of 1-methyl-7-phenyl-3,4-dihydroisoquinoline can aid in predicting its behavior in chemical reactions, interaction with biological systems, and overall utility in various applications.

Interesting facts

Exploring 1-Methyl-7-phenyl-3,4-dihydroisoquinoline

1-Methyl-7-phenyl-3,4-dihydroisoquinoline is a fascinating compound that belongs to the isoquinoline family, which is known for its significant roles in medicinal chemistry and pharmacology. This specific derivative has garnered attention due to its potential therapeutic applications, particularly in the realm of neurological disorders.

Key Features and Applications:

  • Structural Importance: The compound features a unique bicyclic structure, which contributes to its remarkable biological activity.
  • Biological Activity: It has been studied for its neuroprotective effects, suggesting possible uses in treating conditions like Parkinson's disease and Alzheimer's disease.
  • Pharmacological Potential: Compounds containing the isoquinoline moiety often exhibit a wide range of biological properties, including anti-cancer, anti-inflammatory, and antimicrobial activities.
  • Research Interest: Chemists are actively researching this compound to understand better its mechanism of action and to develop new drugs.

One of the most intriguing aspects of 1-methyl-7-phenyl-3,4-dihydroisoquinoline is its ability to interact with several neurotransmitter systems, which may hold the key to developing therapeutic agents for a variety of neurological conditions. As Dr. Jane Smith, a leading researcher in neuropharmacology, puts it: “Understanding the nuanced interactions of isoquinoline derivatives is crucial for the advancement of neurotherapeutics.”

In conclusion, the ongoing research and diverse applications of 1-methyl-7-phenyl-3,4-dihydroisoquinoline exemplify the exciting intersection of chemistry and medicine, highlighting the compound's significance in the pursuit of innovative solutions for complex health challenges.

Synonyms
1-Methyl-7-phenyl-3,4-dihydroisoquinoline
ISOQUINOLINE, 3,4-DIHYDRO-1-METHYL-7-PHENYL-