Interesting facts
Interesting Facts about Methyl 7-(diethylamino)-4-oxo-6-propyl-1H-quinoline-3-carboxylate
Methyl 7-(diethylamino)-4-oxo-6-propyl-1H-quinoline-3-carboxylate is a fascinating compound known for its versatile applications in the field of organic chemistry and medicinal research. Here are some intriguing aspects to consider:
- Quinoline Derivative: This compound belongs to the quinoline class, which is known for its diverse biological activities. Quinoline derivatives have been explored for their potential as antimicrobial, antimalarial, and anticancer agents.
- Biological Relevance: Due to its unique structure, this compound may exhibit interesting pharmacological properties. Scientists continue to research its effects on different biological targets, opening doors for potential therapeutic applications.
- Structure-Activity Relationship (SAR): The specific arrangement of the diethylamino group, propyl side chain, and the carboxylate moiety can significantly influence the compound's activity, allowing chemists to design new derivatives with enhanced efficacy.
- Synthetic Pathways: The synthesis of this compound involves several steps, which may include condensation reactions and modifications typical for quinoline derivatives, making it a subject of interest in synthetic organic chemistry.
- Research Applications: Researchers use this compound as a building block in the development of other more complex structures, often leading to the discovery of new drugs or chemical probes in biological studies.
In summary, methyl 7-(diethylamino)-4-oxo-6-propyl-1H-quinoline-3-carboxylate showcases the interplay between structure and function in medicinal chemistry. As stated by prominent chemists, “The essence of chemistry lies in the manipulation of atoms to solve real-world problems.” This compound exemplifies that essence, paving the way for future discoveries.
Synonyms
AMQUINATE
17230-85-2
Amquinolate
Amquinatum
Anquinato
NSC-339053
Methyl 7-(diethylamino)-4-hydroxy-6-propyl-3-quinolinecarboxylate
21N28Z70CI
DTXSID10169253
3-Quinolinecarboxylic acid 7-(diethylamino)-4-hydroxy-6-propyl-, methyl ester
7-Diethylamino-4-hydroxy-6-propyl-3-quinolinecarboxylic acid methyl ester
DTXCID8091744
NSC339053
Methyl 7-(diethylamino)-4-hydroxy-6-propylquinoline-3-carboxylate
methyl 7-(diethylamino)-4-oxo-6-propyl-1H-quinoline-3-carboxylate
3-Quinolinecarboxylic acid, 7-(diethylamino)-4-hydroxy-6-propyl-, methyl ester
Amquinato
Amquinate (USAN/INN)
Amquinate [USAN:INN]
Amquinatum [INN-Latin]
Amquinato [INN-Spanish]
UNII-21N28Z70CI
NSC 339053
AMQUINATE [INN]
AMQUINATE [USAN]
SCHEMBL537649
CHEMBL2104009
SB72134
DA-43525
NS00124244
D02930
Q27253562
methyl 7-(diethylamino)-4-hydroxy-6-propyl-quinoline-3-carboxylate
Methyl7-(diethylamino)-4-hydroxy-6-propylquinoline-3-carboxylate
Solubility of Methyl 7-(Diethylamino)-4-oxo-6-propyl-1H-quinoline-3-carboxylate
Methyl 7-(diethylamino)-4-oxo-6-propyl-1H-quinoline-3-carboxylate is a complex organic compound whose solubility can be influenced by a variety of factors. Generally, the solubility of such compounds is governed by the following key considerations:
In summary, the solubility of methyl 7-(diethylamino)-4-oxo-6-propyl-1H-quinoline-3-carboxylate can be complex and context-dependent. To assess its solubility more thoroughly, one should consider the particular solvent system in use, as well as the temperature and pH conditions, which can significantly alter the compound's behavior. As with many organic compounds, the interaction between solute and solvent plays a crucial role, making empirical solubility testing essential in practical applications.