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2-(3,3-diphenylallyl)-3,4-dihydroisoquinoline

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Identification
Molecular formula
C24H21N
CAS number
5611-94-9
IUPAC name
2-(3,3-diphenylallyl)-3,4-dihydro-1H-isoquinoline
State
State

At room temperature, 2-(3,3-diphenylallyl)-3,4-dihydroisoquinoline exists in a solid state. It is typically stored in a cool, well-ventilated area to maintain stability.

Melting point (Celsius)
48.00
Melting point (Kelvin)
321.15
Boiling point (Celsius)
406.50
Boiling point (Kelvin)
679.65
General information
Molecular weight
311.42g/mol
Molar mass
311.4150g/mol
Density
1.1020g/cm3
Appearence

The compound appears as a crystalline solid that is typically off-white or pale yellow in color. Its structure includes a 3,3-diphenylallyl chain which extends from the 3,4-dihydroisoquinoline core, contributing to its aromatic appearance.

Comment on solubility

Solubility Profile of 2-(3,3-diphenylallyl)-3,4-dihydro-1H-isoquinoline

The solubility of 2-(3,3-diphenylallyl)-3,4-dihydro-1H-isoquinoline is a complex aspect influenced by its unique structural features. This compound, characterized by its isoquinoline framework and diphenyl substituents, displays varying degrees of solubility in different solvents:

  • Polar solvents: Generally, the solubility in polar solvents such as water is quite limited due to the compound's hydrophobic nature.
  • Non-polar solvents: It tends to demonstrate greater solubility in non-polar organic solvents (e.g., hexane, chloroform), attributable to the substantial aromatic character of the diphenyl groups.
  • Mixed solvents: In solvent systems with moderate polarity (like ethanol), the solubility may improve, suggesting possible intermolecular interactions between the solvent and compound.

As a rule of thumb, one can consider the principle of "like dissolves like":

  1. Non-polar compounds are more soluble in non-polar solvents.
  2. Polar compounds generally dissolve better in polar solvents.

This highlights the importance of solvent selection when predicting solubility behavior for compounds like 2-(3,3-diphenylallyl)-3,4-dihydro-1H-isoquinoline. As a result, thorough understanding and experimentation may be required to determine the best solvent for specific applications involving this compound.

Interesting facts

Interesting Facts about 2-(3,3-diphenylallyl)-3,4-dihydro-1H-isoquinoline

This fascinating compound, 2-(3,3-diphenylallyl)-3,4-dihydro-1H-isoquinoline, belongs to a class of isoquinoline derivatives that exhibit intriguing structural characteristics and biological activities. Here are some captivating insights:

  • Structural Diversity: This compound features a unique combination of an isoquinoline core and a diphenylallyl substituent, which contributes to its diverse chemical behavior and potential applications in various fields.
  • Biological Significance: Isoquinoline derivatives are known for their wide range of biological activities, including antimicrobial, anticancer, and neuroprotective properties. The presence of the diphenylallyl group may enhance its pharmacological profile.
  • Synthetic Pathways: The synthesis of isoquinoline compounds often involves complex multi-step reactions, providing chemists with opportunities to develop novel synthetic methodologies.
  • Pharmacological Research: Investigations into this compound could lead to the discovery of new drugs, particularly those targeting central nervous system disorders, given the relevance of isoquinoline structures in medicinal chemistry.
  • Natural Occurrence: While the compound is synthetically derived, its structural framework is reminiscent of naturally occurring alkaloids, which are often found in a variety of plants and have been traditionally utilized for their therapeutic effects.

In summary, 2-(3,3-diphenylallyl)-3,4-dihydro-1H-isoquinoline is not just a mere chemical structure; it represents a vibrant area of study in organic and medicinal chemistry. As researchers delve deeper into its properties, the potential for discovering new applications continues to expand.

Synonyms
BRN 1435688
4189-79-1
ISOQUINOLINE, 1,2,3,4-TETRAHYDRO-2-(3,3-DIPHENYLALLYL)-
1,2,3,4-Tetrahydro-2-(3,3-diphenylallyl)isoquinoline
2-(3,3-Diphenylallyl)-1,2,3,4-tetrahydroisoquinoline
DTXSID30194663
5-20-06-00324 (Beilstein Handbook Reference)
DTXCID70117154
SCHEMBL24495378
BDBM685747
US12043602, Compound NY0221
2-(3,3-diphenylallyl)-1,2,3,4- tetrahydroisoquinoline