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2-Methylacridine

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Identification
Molecular formula
C14H11N
CAS number
612-10-2
IUPAC name
2-methylacridine
State
State

At room temperature, 2-Methylacridine is in a solid state. The compound is usually handled as a solid powder or crystalline form in laboratory settings.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
241.00
Boiling point (Kelvin)
514.15
General information
Molecular weight
193.26g/mol
Molar mass
193.2640g/mol
Density
1.0774g/cm3
Appearence

2-Methylacridine appears as a pale yellow crystalline solid. It may also be present as a light yellow powder. Under UV light, it exhibits a characteristic fluorescence, which is typical for acridine derivatives.

Comment on solubility

Solubility of 2-methylacridine

2-methylacridine is a heterocyclic organic compound known for its unique structure and properties. When discussing its solubility, several factors come into play:

  • Polar vs Non-polar Solvents: 2-methylacridine is primarily soluble in non-polar solvents due to its aromatic characteristics. It exhibits low solubility in polar solvents like water.
  • Solubility Behavior: As a derivative of acridine, the presence of the methyl group influences its interactions. The compound is often described as having limited solubility in aqueous solutions.
  • Temperature Influence: Like many organic compounds, the solubility of 2-methylacridine can increase with temperature. This behavior underscores the importance of thermal conditions on solubility.

In summary, while 2-methylacridine is not readily soluble in polar solvents such as water, it finds better solubility in organic, non-polar solvents. As with many organic compounds, understanding its solubility characteristics is essential for its application in various chemical processes.

Interesting facts

Interesting Facts about 2-Methylacridine

2-Methylacridine is a fascinating compound within the acridine family, notable for its unique structure and properties. Here are some captivating insights:

  • Structure and Isomerism: As a methyl derivative of acridine, 2-methylacridine's chemical structure features a methyl group located at the second carbon, leading to interesting isomeric forms. The arrangement of atoms in this compound influences its reactivity and stability, making it a subject of numerous studies.
  • Application in Organic Synthesis: This compound is valuable in organic synthesis, acting as a building block for various pharmaceuticals and agrochemicals. Its presence in synthetic pathways has helped chemists develop new therapeutic agents.
  • Biological Activity: Compounds related to acridine have been explored for their biological activity. Some derivatives exhibit antimicrobial and antitumor properties, opening avenues for potential medical applications. Research continues to explore how structural modifications can enhance these effects.
  • Role in Dye Chemistry: 2-Methylacridine has significance in dye chemistry due to its potential use as a dye precursor. This emphasizes its importance in industrial applications, particularly in the dye and pigment sectors.
  • Solubility Behavior: The solubility characteristics of 2-methylacridine can affect its application in various solvents, influencing its reactivity and interaction with other compounds in chemical processes.

In summary, 2-methylacridine is not just a simple derivative of acridine; it embodies a range of chemical behaviors and applications. It demonstrates how subtle changes in molecular structure can lead to significant differences in properties and uses. As new research unfolds, this compound is likely to reveal even more about its capabilities and applications in science.

Synonyms
2-Methylacridine
613-15-0
ACRIDINE, 2-METHYL-
UNII-V6R4PDB5HV
V6R4PDB5HV
NSC 6143
EINECS 210-331-4
BRN 0133145
NSC-6143
METHYLACRIDINE, 2-
DTXSID10210193
5-20-08-00251 (Beilstein Handbook Reference)
DTXCID10132684
210-331-4
hvzwbvzezzjokq-uhfffaoysa-n
NSC6143
SCHEMBL4427125
AKOS006274735
DB-217488
NS00034640
Q27291603