Skip to main content

Ethyl 6,7-diisobutoxy-4-oxo-1H-quinoline-3-carboxylate

ADVERTISEMENT
Identification
Molecular formula
C23H29NO6
CAS number
124809-45-8
IUPAC name
ethyl 6,7-diisobutoxy-4-oxo-1H-quinoline-3-carboxylate
State
State

At room temperature, ethyl 6,7-diisobutoxy-4-oxo-1H-quinoline-3-carboxylate is typically found as a solid. Due to its crystalline nature, it is stable under standard conditions and should be stored in a cool, dry place to maintain its integrity.

Melting point (Celsius)
168.30
Melting point (Kelvin)
441.50
Boiling point (Celsius)
455.50
Boiling point (Kelvin)
728.70
General information
Molecular weight
389.46g/mol
Molar mass
389.4560g/mol
Density
1.1567g/cm3
Appearence

This compound appears as a pale yellow crystalline solid. It is typically used in organic synthesis and could be encountered as a powder or in crystalline form depending on its purity and specific application.

Comment on solubility

Solubility of Ethyl 6,7-Diisobutoxy-4-oxo-1H-Quinoline-3-Carboxylate

The solubility of ethyl 6,7-diisobutoxy-4-oxo-1H-quinoline-3-carboxylate in various solvents can greatly influence its practical applications in chemical processes. Generally, the solubility behavior of such organic compounds is pivotal to understanding their interactions in solution.

Solubility Characteristics

  • Polar Solvents: Compounds containing polar groups typically exhibit higher solubility in polar solvents. However, the presence of isobutoxy substituents may limit solubility in highly polar solvents like water.
  • Non-Polar Solvents: Conversely, the hydrophobic nature imparted by isobutoxy groups may enhance solubility in organic solvents such as ethyl acetate or hexane.
  • Temperature Influence: As with many organic compounds, solubility may increase with temperature, making heating a valuable technique for enhancing dissolution rates.

Moreover, compounds like ethyl 6,7-diisobutoxy-4-oxo-1H-quinoline-3-carboxylate can exhibit varying solubility based on concentration. It's essential to test solubility across different conditions to determine the most suitable solvent for specific applications.

In summary, understanding the solubility profile of this compound is fundamental; as it enhances formulation strategies and improves performance in chemical applications.

Interesting facts

Interesting Facts about Ethyl 6,7-Diisobutoxy-4-Oxo-1H-Quinoline-3-Carboxylate

Ethyl 6,7-diisobutoxy-4-oxo-1H-quinoline-3-carboxylate is a fascinating compound that belongs to the quinoline family, which is notable for its diverse biological activities. Here are some key points that highlight its significance:

  • Pharmacological Potential: Compounds based on the quinoline structure are often explored for their potential as pharmaceuticals. This specific compound may exhibit properties that could lead to the development of new therapeutic agents.
  • Versatile Synthesis: The synthesis of ethyl 6,7-diisobutoxy-4-oxo-1H-quinoline-3-carboxylate involves intricate organic chemistry techniques. Researchers appreciate the methods used to create complex molecules, making this compound a subject of interest in synthetic organic chemistry.
  • Functional Groups: With its diisobutoxy and carboxylate functional groups, this compound is a prime example of how functionalization can significantly enhance the reactivity and solubility of quinoline derivatives.
  • Applications in Research: The quinoline backbone is a common scaffold in medicinal chemistry. Researchers are continually investigating derivatives of quinoline for potential use in cancer therapies, anti-malarial drugs, and antibacterial agents.
  • Structure-Activity Relationship (SAR): The analysis of how variations in the substituents of this compound affect its biological activity is critical for drug design. Studying SAR can lead to the optimization of new compounds with improved efficacy and reduced toxicity.

As we delve deeper into the world of chemical compounds like ethyl 6,7-diisobutoxy-4-oxo-1H-quinoline-3-carboxylate, we unveil a realm of possibilities that advance our understanding of organic compounds and their implications in medicinal chemistry. Each new discovery paves the way for innovative solutions to health-related challenges.

Synonyms
BUQUINOLATE
5486-03-3
Bonaid
Butoril
Bukhinolyat
Buquinolato
Bonaid TM
component of Bonaid
EU-1093
GNF-Pf-1188
NSC-201116
MFL71K7PU4
DTXSID1041689
ethyl 6,7-bis(2-methylpropoxy)-4-oxo-1H-quinoline-3-carboxylate
3-Quinolinecarboxylic acid, 4-hydroxy-6,7-bis(2-methylpropoxy)-, ethyl ester
Ethyl 4-hydroxy-6,7-diisobutoxy-3-quinolinecarboxylate
Ethyl 6,7-diisobutoxy-4-hydroxyquinoline-3-carboxylate
NCGC00167562-01
U 1093
Ethyl 4-hydroxy-6,7-bis(2-methylpropoxy)-3-quinolinecarboxylate
Buchinolatum
Buquinolatum
Caswell No. 447AA
BUQUINOLATE [MI]
BUQUINOLATE [INN]
Buquinolate (USAN/INN)
Buquinolate [USAN:INN]
BUQUINOLATE [USAN]
Buquinolatum [INN-Latin]
UNII-MFL71K7PU4
Buquinolato [INN-Spanish]
Oprea1_292948
Oprea1_346436
CBDivE_003429
BIDD:GT0612
CHEMBL584852
SCHEMBL1404252
BUQUINOLATE [GREEN BOOK]
DTXCID9021689
VUFB 4824
LVVXOXRUTDAKFE-UHFFFAOYSA-N
Eu 1093
EINECS 226-814-8
Tox21_112557
NSC201116
STL513060
AKOS015969691
DB11378
EPA Pesticide Chemical Code 444100
NSC 201116
CAS-5486-03-3
DB-071916
HY-116021
CS-0063540
NS00044584
D03179
Buquinolate, VETRANAL(TM), analytical standard
4-hydroxy-6,7-diisobutoxy-quinoline-3-carboxylic
Q27283997
3-Quinolinecarboxylic acid,7-diisobutoxy-, ethyl ester
3-Quinolinecarboxylic acid, 4-hydroxy-6,7-diisobutoxy-, ethyl ester
3-Quinolinecarboxylic acid,7-bis(2-methylpropoxy)-, ethyl ester
ethyl 4-hydroxy-6,7-bis(2-methylpropoxy)quinoline-3-carboxylate