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Dichlorodimethoxyhydroxybenzoic acid

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Identification
Molecular formula
C9H8Cl2O5
CAS number
28455-12-9
IUPAC name
2,6-dichloro-4-hydroxy-3,5-dimethoxy-benzoic acid
State
State

At room temperature, 2,6-dichloro-4-hydroxy-3,5-dimethoxy-benzoic acid is a solid.

Melting point (Celsius)
242.00
Melting point (Kelvin)
515.00
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.00
General information
Molecular weight
281.07g/mol
Molar mass
281.0670g/mol
Density
1.6730g/cm3
Appearence

2,6-Dichloro-4-hydroxy-3,5-dimethoxy-benzoic acid typically appears as a crystalline solid. It is characterized by its pale yellow color and has a distinctive, sharp odor.

Comment on solubility

Solubility of 2,6-Dichloro-4-hydroxy-3,5-dimethoxy-benzoic Acid

The solubility of 2,6-dichloro-4-hydroxy-3,5-dimethoxy-benzoic acid can be influenced by various factors, making its behavior in different solvents quite interesting:

  • Polar Solvents: Typically, benzoic acid derivatives tend to have better solubility in polar solvents due to their ability to form hydrogen bonds.
  • Non-Polar Solvents: Conversely, these compounds generally exhibit lower solubility in non-polar solvents, given their polar functional groups.
  • Temperature Effect: The solubility can significantly increase with temperature. Higher temperatures often promote dissolution, which can be crucial for applications.
  • pH Influence: The solubility may also vary with pH, particularly if the compound can ionize; in more alkaline conditions, ionization could enhance its solubility.

In summary, the solubility of 2,6-dichloro-4-hydroxy-3,5-dimethoxy-benzoic acid exhibits complex behavior shaped by its molecular structure, the nature of the solvent, and external conditions like temperature and pH. Understanding these aspects is essential for its applications in chemical formulations or medicinal usage.

Interesting facts

Interesting Facts about 2,6-Dichloro-4-hydroxy-3,5-dimethoxy-benzoic Acid

2,6-Dichloro-4-hydroxy-3,5-dimethoxy-benzoic acid is a fascinating compound with a multitude of applications and properties that garner the attention of chemists and researchers alike. Here are some intriguing aspects:

  • Biological Activity: This compound is notable for its role in various biological systems. It has been researched for its potential anti-inflammatory and analgesic properties, making it of interest in pharmaceutical studies.
  • Environmental Impact: The presence of chlorine atoms in the structure often leads to increased stability and persistence in the environment. This characteristic raises questions about the ecological effects of chlorinated compounds and their breakdown products.
  • Structural Features: The compound features a unique combination of hydroxyl and methoxy groups, which can significantly influence its reactivity and interactions with biological molecules, including enzymes and receptors.
  • Synthesis Methods: The synthesis of 2,6-dichloro-4-hydroxy-3,5-dimethoxy-benzoic acid involves multiple steps, including halogenation and demethylation processes. This complexity can provide insights into organic synthesis techniques.
  • Cultural Relevance: Compounds like this are often studied not only for their chemical properties but also for their historical significance in traditional medicine and natural product chemistry.

In summary, 2,6-dichloro-4-hydroxy-3,5-dimethoxy-benzoic acid is more than just a chemical entity; it embodies a range of applications and implications that spark curiosity and promote further investigation in the fields of chemistry and environmental science.

Synonyms
20624-96-8
Benzoic acid, 2,6-dichloro-4-hydroxy-3,5-dimethoxy-
DTXSID60174630