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6-Methyl-2-phenylquinoline

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Identification
Molecular formula
C16H13N
CAS number
1775-42-2
IUPAC name
6-methyl-2-phenyl-quinoline
State
State

At room temperature, 6-Methyl-2-phenylquinoline exists as a solid. Its stability as a solid is typical for compounds with aromatic structures, like quinolines, which are often utilized in chemical research and synthesis due to their solid state.

Melting point (Celsius)
67.00
Melting point (Kelvin)
340.15
Boiling point (Celsius)
342.00
Boiling point (Kelvin)
615.15
General information
Molecular weight
231.30g/mol
Molar mass
231.3020g/mol
Density
1.1010g/cm3
Appearence

6-Methyl-2-phenylquinoline is often found as a crystalline solid. Its crystals are typically colorless to pale yellow, reflecting its purity and chemical structure.

Comment on solubility

Solubility of 6-methyl-2-phenyl-quinoline

6-methyl-2-phenyl-quinoline is an organic compound that exhibits interesting solubility characteristics. It is important to consider the following key points regarding its solubility:

  • Solvent Polarity: The solubility of 6-methyl-2-phenyl-quinoline is highly influenced by the polarity of the solvent used. Generally, it is more soluble in non-polar solvents such as hexane and toluene due to its hydrophobic nature.
  • Hydrogen Bonding: This compound has limited capacity for hydrogen bonding, which affects its solubility in polar solvents like water. As a result, it has low solubility in such media.
  • Concentration Effects: When dissolved in organic solvents, increasing the concentration of the compound can lead to partial precipitation, highlighting its solubility limit.

In summary, "like dissolves like" applies to 6-methyl-2-phenyl-quinoline; hence, it is best dissolved in non-polar environments. Understanding these solubility characteristics is essential for applications in synthesis and analysis.

Interesting facts

Interesting Facts about 6-methyl-2-phenyl-quinoline

6-methyl-2-phenyl-quinoline is a fascinating compound that belongs to the class of quinoline derivatives, which are known for their significance in various fields, including medicinal chemistry and organic synthesis. Here, we explore some engaging aspects of this compound:

  • Structure and Function: The structure of 6-methyl-2-phenyl-quinoline consists of a quinoline backbone with a phenyl group and a methyl group attached. This specific arrangement of atoms contributes to its unique properties, making it an interesting subject for study.
  • Biological Activity: Quinoline derivatives have been reported to exhibit diverse biological activities. Compounds similar to 6-methyl-2-phenyl-quinoline are of particular interest in pharmaceutical research for their potential as anti-cancer, anti-inflammatory, and antimicrobial agents.
  • Applications in Organic Synthesis: 6-methyl-2-phenyl-quinoline can serve as a valuable intermediate in organic synthesis, playing a crucial role in developing other complex molecules used in various applications, such as medicinal drugs and agrochemicals.
  • Fluorescent Properties: Some quinoline derivatives are known for their fluorescent properties, which can be beneficial in biological imaging and sensing applications, allowing scientists to study cellular processes in real-time.

In summary, 6-methyl-2-phenyl-quinoline stands out as a compound of interest due to its structural characteristics and potential applications in medicinal chemistry and organic synthesis. As researchers continue to explore the properties of quinoline derivatives, we may uncover even more astonishing uses and benefits that could impact various scientific fields.

Synonyms
6-METHYL-2-PHENYLQUINOLINE
27356-46-3
6-Methyl-2-phenyl-quinoline
Quinoline, 6-methyl-2-phenyl-
2-phenyl-6-methyl-quinoline
6-Methyl-2-phenylquinoline #
CHEMBL459923
SCHEMBL8830002
SCHEMBL8830006
SCHEMBL29692924
DTXSID60181788
SBB095808
AKOS016002921
AC-9586
SB70542
DA-19538
AN-829/42535952