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2,3-Dimethylquinoline

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Identification
Molecular formula
C11H11N
CAS number
1198-37-4
IUPAC name
2,3-dimethylquinoline
State
State

Under standard conditions of temperature and pressure, 2,3-Dimethylquinoline is a liquid. It is volatile and has a moderate vapor pressure, resulting in the capacity to evaporate into the air.

Melting point (Celsius)
-7.10
Melting point (Kelvin)
266.05
Boiling point (Celsius)
253.00
Boiling point (Kelvin)
526.15
General information
Molecular weight
157.21g/mol
Molar mass
157.2110g/mol
Density
1.0079g/cm3
Appearence

2,3-Dimethylquinoline is typically a colorless to light yellow liquid. It may darken upon exposure to air and light. It has a characteristic aromatic odor.

Comment on solubility

Solubility of 2,3-Dimethylquinoline

2,3-Dimethylquinoline, with its intriguing structure, exhibits interesting solubility characteristics that are crucial for various applications. This compound is primarily known for its moderate solubility profiles, which can be summarized as follows:

  • Solvent Interaction: 2,3-Dimethylquinoline is generally soluble in organic solvents such as ethanol, acetone, and chloroform. However, it displays limited solubility in polar solvents like water.
  • Molecular Structure Influence: The presence of both methyl groups and the quinoline ring system affects its overall hydrophobic nature, contributing to its reluctance to dissolve in high-polarity environments.
  • Practical Implications: The solubility behavior has significant implications in chemical reactions, synthesis processes, and applications in fields like pharmaceuticals and material sciences.

To summarize, while 2,3-dimethylquinoline is soluble in certain organic solvents, its limited solubility in water showcases the general behavior of quinoline derivatives. Researchers and chemists often need to consider these factors when designing experiments or formulations involving this compound.

Interesting facts

Interesting Facts About 2,3-dimethylquinoline

2,3-dimethylquinoline is a fascinating compound belonging to the quinoline family, which is known for its aromatic properties and diverse applications in organic chemistry. Here are some key points of interest regarding this compound:

  • Aromatic Nature: Quinoline derivatives, including 2,3-dimethylquinoline, exhibit a unique aromatic character due to their fused ring structure, which contributes to their stability and reactivity.
  • Biological Significance: Many quinoline compounds have been studied for their biological activities. For instance, compounds related to 2,3-dimethylquinoline have been researched for potential antimalarial and antitumor properties.
  • Applications in Organic Synthesis: This compound can serve as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, showcasing its utility in the field of medicinal chemistry.
  • Fluorescent Properties: Some derivatives of quinoline are known to exhibit fluorescence, making them valuable in analytical chemistry and as fluorescent probes.
  • Environmental Studies: Quinoline compounds, including 2,3-dimethylquinoline, can be found in coal tar and are studied for their environmental impact, particularly in relation to pollution and biodegradation.

With its diverse applications and significant presence in both natural and synthetic environments, 2,3-dimethylquinoline presents an exciting area of study for chemists and researchers seeking to unlock its full potential.

Synonyms
2,3-DIMETHYLQUINOLINE
1721-89-7
Quinoline, 2,3-dimethyl-
EINECS 217-016-0
DTXSID00169207
DTXCID5091698
217-016-0
fbofhvfmpnnikn-uhfffaoysa-n
MFCD03085977
SCHEMBL422035
BAA72189
AKOS005079387
SB68504
DB-081648
CS-0258436
NS00010749
EN300-701405
G71553
AO-801/41077381
11T-0826