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2,6-Dimethylquinoline

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Identification
Molecular formula
C11H11N
CAS number
877-43-0
IUPAC name
2,6-dimethylquinoline
State
State

At room temperature, 2,6-Dimethylquinoline is in a liquid state. It is typically used in chemical synthesis and can be found as a stable liquid under standard conditions of temperature and pressure.

Melting point (Celsius)
-3.00
Melting point (Kelvin)
270.15
Boiling point (Celsius)
263.00
Boiling point (Kelvin)
536.15
General information
Molecular weight
157.22g/mol
Molar mass
157.2210g/mol
Density
1.0020g/cm3
Appearence

2,6-Dimethylquinoline appears as a yellow to light brown liquid. It has an aromatic odor characteristic of quinoline derivatives.

Comment on solubility

Solubility of 2,6-Dimethylquinoline

2,6-Dimethylquinoline, with the chemical formula C10H9N, is an organic compound belonging to the quinoline family. Its solubility characteristics are influenced by several factors:

  • Polar Nature: Due to the presence of a nitrogen atom in its aromatic structure, 2,6-dimethylquinoline exhibits some polar characteristics, which can contribute to its solubility in polar solvents.
  • Solvent Interactions: It is generally more soluble in organic solvents such as ethanol and acetone compared to water. The aromatic rings in the compound facilitate interactions with these non-polar to slightly polar solvents.
  • Hydrophobic Effects: The overall hydrophobic nature of the compound limits its solubility in aqueous solutions. Therefore, you may find that it has low solubility in water, making it a poor candidate for aqueous reactions.

In summary, while 2,6-dimethylquinoline shows reasonable solubility in organic solvents, its low solubility in water underscores the importance of considering solvent choice in chemical reactions and applications. As with many organic compounds, understanding the solubility profile aids in predicting behavior in various chemical environments.

Interesting facts

Interesting Facts about 2,6-dimethylquinoline

2,6-dimethylquinoline is a fascinating compound that belongs to the quinoline family, which is known for its diverse applications in various fields. This aromatic heterocyclic compound is notable for its unique structure, featuring a fused benzene and pyridine ring.

Key Characteristics

  • Biological Activity: Compounds like 2,6-dimethylquinoline have shown potential in medicinal chemistry, exhibiting antimicrobial and anticancer properties. Researchers are continually exploring its ability to act as a lead compound in drug development.
  • Role in Organic Synthesis: This compound serves as an intermediate in the synthesis of more complex organic molecules, making it a valuable asset in the field of organic chemistry.
  • Fluorescence: 2,6-dimethylquinoline displays interesting fluorescent characteristics, leading to applications in fluorescence microscopy and other analytical techniques.
  • Ligand Potential: It can act as a ligand in coordination chemistry, binding metals and showing potential usage in creating metal complexes for various applications.

Interesting Quote

"The study of quinolines and their derivatives opens the door to a wealth of potential in pharmaceuticals, materials science, and beyond."

In summary, 2,6-dimethylquinoline is not just a simple organic compound but a crucial player in advancing research in chemistry and medicine. Its multifaceted nature continues to intrigue scientists and students alike!

Synonyms
2,6-DIMETHYLQUINOLINE
6-Methylquinaldine
Quinoline, 2,6-dimethyl-
p-Toluquinaldine
2,6-dimethyl quinoline
UNII-KST0M1T4MB
KST0M1T4MB
NSC 1782
NSC-1782
EINECS 212-891-5
Quinoline, 2,6-dimethyl
AI3-03277
DTXSID0044153
pToluquinaldine
6Methylquinaldine
26-Dimethylquinoline
26-Dimethyl-quinoline
Quinoline, 2,6dimethyl
DTXCID8024153
212-891-5
jjpszkiogbrmhk-uhfffaoysa-n
877-43-0
2,6-Dimethyl-quinoline
MFCD00006762
CHEMBL194502
2.6-Dimethylquinoline
Quinoline,6-dimethyl-
BIDD:GT0805
SCHEMBL161703
2,6-Dimethylquinoline, 98%
NSC1782
BBL034645
BDBM50159273
STL420576
AKOS000121619
CS-W010911
HY-W010195
SB67469
NCGC00334900-01
AS-48061
PD158272
SY016998
DB-057018
D1236
EU-0000308
NS00039217
EN300-17623
F17612
6-Methylquinaldine; NSC 1782; p-Toluquinaldine
AB01326686-02
Q27282416
Z56969311