Interesting facts
Exploring 2-(4-Methylpiperazin-1-yl)quinoline
2-(4-Methylpiperazin-1-yl)quinoline is an intriguing compound that merges the structural features of both quinoline and piperazine moieties, showcasing a variety of fascinating attributes. Here are some key insights into this remarkable compound:
- Pharmacological Significance: Compounds with a quinoline backbone are recognized for their biological activities, including their roles as antibacterial, antimalarial, and anti-inflammatory agents. The presence of the piperazine group enhances the pharmacological profile, making this compound a candidate for drug development.
- Versatile Applications: Beyond medicinal chemistry, 2-(4-Methylpiperazin-1-yl)quinoline may find use in the field of materials science. Its ability to interact with various biological substrates can lead to innovative applications in biochemistry and nanotechnology.
- Structure-Activity Relationship: Chemists are particularly interested in the structural diversity of quinoline derivatives. 2-(4-Methylpiperazin-1-yl)quinoline's unique molecular structure allows researchers to study how modifications can affect its pharmacological activity, providing insight into structure-activity relationships (SAR).
- Synthesis and Modifications: The synthetic pathways to create this compound often involve multi-step reactions, showcasing the challenge and creativity required in organic synthesis. This provides opportunities for chemistry students to engage in practical learning experiences.
- Research Potential: With ongoing studies evaluating the therapeutic potential of various quinoline derivatives, 2-(4-Methylpiperazin-1-yl)quinoline remains an exciting subject for current and future research endeavors. Scientists are continually investigating its properties and exploring new derivatives for enhanced efficacy.
In conclusion, 2-(4-Methylpiperazin-1-yl)quinoline stands as an example of the rich interplay between structure and function in chemical compounds. Its role in pharmaceutical research, combined with its intriguing synthetic pathways, makes it a captivating topic for both seasoned chemists and emerging students in the field.
Synonyms
N-methylquipazine
2-(4-methylpiperazin-1-yl)quinoline
28614-26-8
quinoline, 2-(4-methyl-1-piperazinyl)-
0YV1ZIR6S0
CHEMBL288591
CHEBI:64164
1-(2-Quinolyl)-4-methylpiperazine
J366.838J
2-(4-Methyl-piperazin-1-yl)-quinoline
2-(1-(4-methyl)-piperazinyl)quinoline
Tocris-0566
Lopac-Q-107
Biomol-NT_000084
UNII-0YV1ZIR6S0
Lopac0_001000
Oprea1_654246
SCHEMBL606721
BPBio1_001081
DTXSID8043731
HOMWNUXPSJQSSU-UHFFFAOYSA-N
2-(4-Methylpiperazinyl)-quinoline
BDBM50053631
STK362919
AKOS005453926
CCG-205080
NCGC00015867-01
NCGC00015867-02
NCGC00015867-03
NCGC00015867-04
NCGC00024653-01
NCGC00024653-02
NCGC00024653-03
EN300-14327696
BRD-K62056274-001-01-9
BRD-K62056274-332-01-8
Q27133086
Z31193883
Solubility of 2-(4-methylpiperazin-1-yl)quinoline
The solubility of the compound 2-(4-methylpiperazin-1-yl)quinoline, with the chemical formula C14H17N3, plays a crucial role in its practical applications, particularly in pharmaceutical formulations. Understanding its solubility characteristics can help predict its behavior in various solvents.
Key Points on Solubility:
As a general observation, compounds like 2-(4-methylpiperazin-1-yl)quinoline often demonstrate a solubility profile that is
*higher in organic solvents* and *lower in water*, which is common for many aromatic amines. As such, conducting experiments under varying conditions will provide a clearer understanding of this compound’s solubility.