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2-Bromo-6-chlorobenzoic acid

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Identification
Molecular formula
C7H4BrClO2
CAS number
19877-31-3
IUPAC name
2-bromo-6-chloro-benzoic acid
State
State

At room temperature, 2-bromo-6-chlorobenzoic acid is typically a solid.

Melting point (Celsius)
157.00
Melting point (Kelvin)
430.15
Boiling point (Celsius)
255.00
Boiling point (Kelvin)
528.15
General information
Molecular weight
251.45g/mol
Molar mass
251.4530g/mol
Density
1.8080g/cm3
Appearence

2-Bromo-6-chlorobenzoic acid appears as a white to light yellow crystalline powder.

Comment on solubility

Solubility of 2-bromo-6-chloro-benzoic acid

2-bromo-6-chloro-benzoic acid, with the chemical formula C7H4BrClO2, exhibits intriguing solubility properties that are essential to its applications in various chemical processes. Its solubility can be influenced by several factors:

  • Polarity: The presence of both the bromo and chloro substituents, along with the carboxylic acid group, contributes to the molecule's polar characteristics. This can hinder solubility in non-polar solvents.
  • Solvent Type: Generally, 2-bromo-6-chloro-benzoic acid is more soluble in polar solvents such as:
    • Water
    • Ethanol
    • Methanol
  • Temperature: Increasing temperature usually enhances solubility in many solvents. Therefore, heating the solvent may aid in dissolving the compound more effectively.

On the contrary, this compound may have limited solubility in non-polar solvents, which makes it less favorable for use in lipid-based systems. As a rule of thumb, the solubility of benzoic acids is closely related to their molecular structure and the presence of functional groups, making 2-bromo-6-chloro-benzoic acid a good candidate for reactions requiring a soluble benzoic acid derivative. Understanding these solubility characteristics is vital for chemists looking to optimize reactions involving this compound.

Interesting facts

Interesting Facts about 2-bromo-6-chloro-benzoic acid

2-bromo-6-chloro-benzoic acid is a fascinating compound that belongs to the family of benzoic acids. This compound is noteworthy not just for its chemical structure, but also for its diverse applications and reactivity. Here are some intriguing points about this compound:

  • Reactivity: 2-bromo-6-chloro-benzoic acid contains both bromine and chlorine substituents, which can significantly influence its reactivity. These halogen atoms can participate in various chemical reactions, making the compound a useful intermediate in organic synthesis.
  • Applications: Due to its unique structure, this compound is often utilized in the synthesis of pharmaceutical compounds and agrochemicals. The presence of carboxylic acid functional groups allows for further modifications, ultimately leading to the development of biologically active molecules.
  • Biochemistry: Research has shown that similar compounds can play critical roles in enzyme inhibition. Given its structural features, 2-bromo-6-chloro-benzoic acid may have potential as a lead compound in drug discovery processes.
  • Synthesis: The synthesis of 2-bromo-6-chloro-benzoic acid can be achieved through multiple methods, including electrophilic aromatic substitution. The ability to introduce halogens onto an aromatic ring highlights the versatility of aromatic chemistry.
  • Environmental Impact: As with many halogenated compounds, studies on the environmental impact of 2-bromo-6-chloro-benzoic acid are necessary. Researchers must consider its persistence and possible effects within ecosystems.

In conclusion, 2-bromo-6-chloro-benzoic acid is more than just a simple aromatic compound. It offers vast opportunities for exploration in synthetic chemistry, medicinal applications, and environmental studies. As scientists and students alike delve into the world of chemical compounds, discoveries surrounding such molecules highlight the intricate and dynamic nature of chemistry!

Synonyms
2-bromo-6-chlorobenzoic acid
DTXSID40275018
RefChem:466997
DTXCID20202044
622-296-6
93224-85-2
Benzoic acid, 2-bromo-6-chloro-
MFCD00672929
6-bromo-2-chloroBenzoic acid
2-bromo-6-chloro-benzoic acid
2-Bromo-6-chlorobenzoic acid; NSC 190301
2-Bromo-6-chlorobenzoicacid
NSC190301
SCHEMBL696250
62KG5T44XB
URGXUQODOUMRFP-UHFFFAOYSA-N
BBL025943
SBB064721
STL367210
2-Bromo-6-chlorobenzoic acid, 97%
AKOS004115240
CS-W012889
MB01394
NSC-190301
AC-26004
SY023708
TS-03316
DB-006019
EN300-109511
224B852
F019332