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2-Benzoyl-5-chlorobenzoic acid

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Identification
Molecular formula
C14H9ClO3
CAS number
50367-22-3
IUPAC name
2-benzoyl-5-chloro-benzoic acid
State
State

At room temperature, 2-Benzoyl-5-chlorobenzoic acid is in a solid state, typically in the form of a crystalline powder.

Melting point (Celsius)
165.00
Melting point (Kelvin)
438.15
Boiling point (Celsius)
430.00
Boiling point (Kelvin)
703.15
General information
Molecular weight
262.68g/mol
Molar mass
262.6890g/mol
Density
1.4290g/cm3
Appearence

2-Benzoyl-5-chlorobenzoic acid typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-benzoyl-5-chloro-benzoic acid

2-benzoyl-5-chloro-benzoic acid, a benzoic acid derivative, exhibits unique solubility characteristics that are significant to its application in various chemical processes. The solubility of this compound can be influenced by several factors:

  • Polar vs. Nonpolar Solvents: Due to its carboxylic acid functionality, 2-benzoyl-5-chloro-benzoic acid is generally more soluble in polar solvents such as water and alcohols compared to nonpolar solvents.
  • pH Influence: The solubility can increase considerably in basic solutions where the carboxylic acid group is deprotonated, converting it into its more soluble salt form.
  • Temperature Effects: Like many organic compounds, increasing the temperature usually enhances solubility, making this acid dissolve more readily in solvents at elevated temperatures.
  • Crystal Lattice Energy: The solid-state interactions and crystal packing may influence the solubility; compact structures tend to exhibit lower solubility.

In summary, the solubility of 2-benzoyl-5-chloro-benzoic acid can be enhanced under the right conditions, emphasizing the importance of selecting appropriate solvents and manipulating environmental variables when working with this compound.

Interesting facts

Interesting Facts About 2-benzoyl-5-chloro-benzoic acid

2-benzoyl-5-chloro-benzoic acid is a fascinating compound that finds its application in various fields of chemistry and industry. Here are some intriguing insights:

  • Structural Significance: This compound features a unique combination of a benzoyl group and a chloro substitution, contributing to its theoretical and practical importance. The presence of both a carbonyl (C=O) and a carboxylic acid group (-COOH) enhances its reactivity.
  • Synthesis: 2-benzoyl-5-chloro-benzoic acid can be synthesized through various methods, typically involving Friedel-Crafts acylation. This process effectively introduces the benzoyl group onto the aromatic ring, demonstrating the versatile nature of aromatic compounds in organic synthesis.
  • Applications: This compound has potential applications in pharmaceuticals and agricultural chemistry. Its structural characteristics make it a candidate for developing new drug formulations or as a chemical intermediate.
  • Photochemical Properties: The presence of aromatic rings allows this compound to absorb UV light effectively. As a result, it may play a role in various photochemical processes or serve as a photostabilizer in certain materials.
  • Environmental Considerations: As with many organic compounds, the environmental impact and degradation pathway of 2-benzoyl-5-chloro-benzoic acid merit investigation. Understanding how this compound interacts with environmental systems is crucial for assessing its safety and ecological footprint.

The study of 2-benzoyl-5-chloro-benzoic acid exemplifies the intersection of organic synthesis and practical application, making it a worthwhile topic for both students and seasoned chemists alike. Its diverse characteristics not only highlight the depth of organic chemistry but also encourage further exploration and research into its benefits and implications.

Synonyms
BENZOIC ACID, 2-BENZOYL-5-CHLORO-
1147-42-8
BRN 0652289
4-Chlorobenzophenone-2-carboxylic acid
DTXSID60150833
DTXCID0073324
2-benzoyl-5-chlorobenzoic acid
SCHEMBL3956037
CHEMBL2260707
STR00283
AKOS037655867