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(7-nitro-8-quinolyl) 2-chlorobenzoate

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Identification
Molecular formula
C16H9ClN2O4
CAS number
67669-10-5
IUPAC name
(7-nitro-8-quinolyl) 2-chlorobenzoate
State
State

At room temperature, (7-nitro-8-quinolyl) 2-chlorobenzoate is typically found in a solid state. Its crystalline formation makes it relatively stable under ambient conditions.

Melting point (Celsius)
212.00
Melting point (Kelvin)
485.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
318.70g/mol
Molar mass
318.7160g/mol
Density
1.4256g/cm3
Appearence

The compound commonly presents as a complex crystalline solid, often exhibiting a light yellow to yellow coloration. It typically appears as fine powdery crystals or small granules.

Comment on solubility

Solubility of (7-nitro-8-quinolyl) 2-chlorobenzoate

The solubility of (7-nitro-8-quinolyl) 2-chlorobenzoate can be influenced by several factors, including its molecular structure and the polarity of the solvent. Generally, this compound exhibits:

  • Moderate solubility in organic solvents: Due to the presence of non-polar aromatic systems, it tends to dissolve well in non-polar or slightly polar organic solvents such as dichloromethane and ethyl acetate.
  • Low solubility in water: The presence of multiple aromatic rings and the halogen atom can hinder its interaction with water molecules, resulting in very low solubility in aqueous environments.

It's important to note that the solubility may vary with temperature and the nature of the solvent. As a rule of thumb:

  1. Increases in temperature can often lead to increased solubility for many organic compounds.
  2. Polarity of the solvent should be considered: like dissolves like, meaning non-polar compounds will generally dissolve in non-polar solvents.

The observed solubility characteristics are crucial for applications in fields such as organic synthesis and medicinal chemistry. Understanding these properties allows chemists to choose appropriate solvents for reactions and extractions involving (7-nitro-8-quinolyl) 2-chlorobenzoate.

Interesting facts

Interesting Facts about (7-nitro-8-quinolyl) 2-chlorobenzoate

(7-nitro-8-quinolyl) 2-chlorobenzoate is an intriguing compound within the realm of organic chemistry, recognized for its multifaceted applications and structural uniqueness. Here are several captivating aspects about this compound:

  • Functional Groups: This compound features both a nitro group and a chlorobenzoate moiety. These functional groups contribute to its reactivity and potential utility in various chemical reactions.
  • Fluorescent Properties: The quinoline structure is known for its fluorescence. Compounds like (7-nitro-8-quinolyl) 2-chlorobenzoate may exhibit fluorescent properties, making them useful in areas such as biochemical sensing and imaging.
  • Biological Activity: Many quinoline derivatives are studied for their biological activities, including antimicrobial and antitumor effects. The incorporation of a nitro group may enhance their activity, signaling potential pharmaceutical applications.
  • Synthesis: The synthesis of this compound generally involves multiple steps, requiring careful consideration of reaction conditions. This offers students and chemists a practical example of design and methodology in synthetic organic chemistry.
  • Research Potential: Ongoing research into quinolyl derivatives highlights their importance in materials science and medicinal chemistry. They continue to be subjects of interest for creating new therapeutic agents.

As a scientist or a chemistry student, exploring (7-nitro-8-quinolyl) 2-chlorobenzoate can broaden your understanding of the relationship between chemical structure and function, as well as the broader implications of organic compounds in everyday applications.

Synonyms
BENZOIC ACID, o-CHLORO-, 7-NITRO-8-QUINOLYL ESTER
29007-04-3
BRN 1549401
8-Quinolinol, 7-nitro-, o-chlorobenzoate
o-Chlorobenzoic acid 7-nitro-8-quinolyl ester
SCHEMBL4458598
DTXSID40183225