Product name:4-AMINO-2-METHYLQUINOLINE
Synonymous:LABOTEST-BBLT02084860;AKOSAUF2104;4-AMINOQUINALDINE;4-AMINO-2-METHYLQUINOLINE;TIMTEC-BBSBB003992;2-Methyl-4-quinolinamine;4-Quinolinamine,2-methyl-;2-METHYLQUINOLIN-4-YLAMINE
CAS No.:6628-04-2
Molecular formula:C10H10N2
Molecular weight:158.2
EINECS No.:229-604-4
Application: intermediate of Dequalinium chloride
*The following content is generated by AI and is for reference only.
4-Amino-2-methylquinoline is a versatile heterocyclic compound belonging to the quinoline family, widely recognized for its significance in organic synthesis and medicinal chemistry. With the chemical formula C10H10N2 and CAS Registry Number 933-67-5, this substance features an amino group at the fourth position and a methyl substituent at the second position of the quinoline ring system. Its molecular structure imparts unique electronic and steric properties, making it an essential building block for constructing more complex nitrogen-containing architectures.
The primary application of 4-amino-2-methylquinoline lies in the pharmaceutical industry, where it serves as a key intermediate for synthesizing bioactive molecules. Researchers frequently utilize this compound to develop antimalarial agents, anticancer drugs, and antimicrobial therapeutics due to the inherent biological activity associated with the quinoline scaffold. The presence of the amino group facilitates various coupling reactions, such as diazotization and azo coupling, enabling the creation of dyes, pigments, and fluorescent probes used in analytical chemistry and materials science. Furthermore, derivatives of this molecule have shown promise in developing agrochemicals, including herbicides and fungicides, contributing to agricultural productivity.
In academic research, 4-amino-2-methylquinoline is valued for studying reaction mechanisms and exploring novel synthetic pathways. Its stability under standard conditions allows for easy handling and storage, while its reactivity supports diverse chemical transformations. As a precursor, it plays a critical role in the production of advanced functional materials and coordination complexes. Despite its specialized nature, the compound remains accessible through commercial suppliers, ensuring availability for both small-scale laboratory experiments and large-scale industrial processes. Ongoing investigations continue to uncover new applications, reinforcing its status as a fundamental component in modern chemical innovation. Whether utilized in drug discovery or material development, 4-amino-2-methylquinoline exemplifies the intersection of structural simplicity and functional complexity in heterocyclic chemistry.