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(7-nitro-8-quinolyl) 4-chlorobenzoate

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Identification
Molecular formula
C16H9ClNO4
CAS number
467458-09-7
IUPAC name
(7-nitro-8-quinolyl) 4-chlorobenzoate
State
State

Generally, (7-nitro-8-quinolyl) 4-chlorobenzoate is a solid at room temperature. The compound is stable under standard laboratory conditions and is used in various organic reactions and research applications. It is important to handle the compound with care, taking note of its reactivity and potential hazards due to the nitro group.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
550.00
Boiling point (Kelvin)
823.15
General information
Molecular weight
314.70g/mol
Molar mass
314.7170g/mol
Density
1.4000g/cm3
Appearence

(7-Nitro-8-quinolyl) 4-chlorobenzoate typically appears as a solid compound. The appearance can vary depending on the form, such as crystalline or powder, and might exhibit a light color, often related to its aromatic structure combined with nitro groups.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 4-chlorobenzoate

(7-nitro-8-quinolyl) 4-chlorobenzoate is an intriguing compound with unique solubility characteristics. Understanding its solubility is essential for various applications in chemical synthesis and formulation.

This compound generally exhibits the following solubility profile:

  • Polar Solvents: It tends to have limited solubility in polar solvents, such as water, due to its hydrophobic nature attributed to the quinoline ring structure.
  • Organic Solvents: However, it shows improved solubility in organic solvents like dichloromethane, ethyl acetate, and acetone, which can effectively solubilize such aromatic compounds.
  • Aqueous Solutions: In aqueous solutions, the presence of nitro and chloro groups may hinder solubility because they influence the interaction with water molecules.

Moreover, as with many organic compounds, solubility can be influenced by temperature and the presence of other solutes. For example:

  1. Increasing temperature often increases solubility.
  2. The addition of co-solvents can enhance solubility in mixed solvent systems.

The study of its solubility is crucial because it affects reaction rates and bioavailability in pharmaceutical applications. Therefore, understanding and optimizing the solubility of (7-nitro-8-quinolyl) 4-chlorobenzoate can lead to more effective utilization of this compound in various fields.

Interesting facts

Interesting Facts about (7-nitro-8-quinolyl) 4-chlorobenzoate

(7-nitro-8-quinolyl) 4-chlorobenzoate is a fascinating compound that blends the properties of quinoline and benzoate derivatives. Its unique structure lends it specific characteristics and potential applications that intrigue chemists and researchers alike.

Key Features

  • Bioactivity: This compound is often studied for its potential biological activities, including anti-bacterial and anti-fungal properties. Such activities are attributed to its ability to interact with various biological targets.
  • Photophysical Properties: The compound exhibits interesting photophysical characteristics, making it useful in fields like fluorescent probes and sensors.
  • Versatile Synthesis: The synthesis of (7-nitro-8-quinolyl) 4-chlorobenzoate can be achieved using various methods, highlighting its versatility in chemical synthesis.

Researchers have reported intriguing findings regarding its reactivity and utility. For instance, it has been noted that compounds containing the quinoline moiety can partake in *metal coordination* and *ligand exchange* processes, which can be of significant interest in coordination chemistry.

Applications

  • Pharmaceutical Development: Its structure positions it as a candidate for drug development, particularly in the realm of anti-infective agents.
  • Material Science: This compound's unique properties may also find applications in the development of advanced materials, such as organic light-emitting diodes (OLEDs).

In conclusion, the exploration of (7-nitro-8-quinolyl) 4-chlorobenzoate not only sheds light on its functional capabilities but also emphasizes the broader significance of quinoline derivatives in modern chemistry. This compound is a prime example of how specific chemical structures can lead to innovative applications and deepen our understanding of biological processes.

Synonyms
BENZOIC ACID, p-CHLORO-, 7-NITRO-8-QUINOLYL ESTER
29007-02-1
BRN 1548657
8-Quinolinol, 7-nitro-, p-chlorobenzoate
p-Chlorobenzoic acid, 7-nitro-8-quinolyl ester
SCHEMBL4457912
DTXSID20183223