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(7-nitro-8-quinolyl) 3-chlorobenzoate

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Identification
Molecular formula
C16H9ClN2O4
CAS number
34562-31-7
IUPAC name
(7-nitro-8-quinolyl) 3-chlorobenzoate
State
State

This compound is typically a solid at room temperature, maintaining its integrity as a bright yellow crystalline powder.

Melting point (Celsius)
165.00
Melting point (Kelvin)
438.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
346.72g/mol
Molar mass
346.7210g/mol
Density
1.4623g/cm3
Appearence

(7-Nitro-8-quinolyl) 3-chlorobenzoate presents itself as a yellow crystalline solid. The compound is stable and exhibits typical behaviors of aromatic esters under normal conditions.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 3-chlorobenzoate

The solubility of (7-nitro-8-quinolyl) 3-chlorobenzoate is a subject of interest in various chemical contexts. This compound exhibits variable solubility characteristics depending on the solvent used. Understanding its solubility can be categorized as follows:

  • Polar solvents: The presence of both nitro and chloro functional groups in the structure can enhance solubility in polar solvents due to dipole-dipole interactions.
  • Non-polar solvents: Conversely, this compound may have limited solubility in non-polar organic solvents, which typically do not stabilize ionic or polar compounds effectively.
  • pH Influence: The solubility may also be affected by the pH of the solution, as protonation can enhance or inhibit solubility for compounds containing nitrogen heterocycles.

In summary, the solubility of (7-nitro-8-quinolyl) 3-chlorobenzoate is influenced by its molecular structure and the properties of the solvent. Overall, it is essential to consider these factors for applications in organic synthesis and pharmaceutical formulations.

Interesting facts

Exploring (7-nitro-8-quinolyl) 3-chlorobenzoate

(7-nitro-8-quinolyl) 3-chlorobenzoate is a fascinating compound that belongs to the quinoline family and offers multiple applications in various fields, particularly in medicinal chemistry. Here are some intriguing aspects of this compound:

  • Versatile Applications: Compounds containing quinoline structures have been widely investigated for their potential as pharmaceutical agents. This particular compound may exhibit antimicrobial, antimalarial, and anticancer properties.
  • Electrochemical Properties: The presence of the nitro group and quinoline structure can enhance its electrochemical behavior, making it a candidate for use in sensors or photoactive materials.
  • Binding Affinity: Studies have shown that quinoline derivatives often display strong binding affinities to biological targets, including enzymes and receptors, which may lead to new therapeutic strategies.
  • Research Potential: As a derivative of benzoate, this compound could serve as a scaffold for the design of new compounds with improved biological activity, providing a pathway for novel drug discovery.

The synthesis of (7-nitro-8-quinolyl) 3-chlorobenzoate generally involves well-established methods in organic chemistry, enabling researchers to manipulate the structure for various potential outcomes. As stated in a recent study, "Quinoline derivatives continue to push the frontiers of medicinal chemistry, offering new hope for treating challenging diseases."

With ongoing research showcasing the dynamic nature of this compound, (7-nitro-8-quinolyl) 3-chlorobenzoate stands out as a promising structure for further exploration in the quest for innovative pharmaceutical solutions.

Synonyms
BENZOIC ACID, m-CHLORO-, 7-NITRO-8-QUINOLYL ESTER
29007-03-2
BRN 1548655
8-Quinolinol, 7-nitro-, m-chlorobenzoate
m-Chlorobenzoic acid 7-nitro-8-quinolyl ester
SCHEMBL4461261
DTXSID80183224