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2,4-dibromo-6-chlorophenol

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Identification
Molecular formula
C6H3Br2ClO
CAS number
2050-20-6
IUPAC name
2,4-dibromo-6-chloro-phenol
State
State
2,4-dibromo-6-chlorophenol is typically a solid at room temperature.
Melting point (Celsius)
87.00
Melting point (Kelvin)
360.15
Boiling point (Celsius)
326.00
Boiling point (Kelvin)
599.15
General information
Molecular weight
302.32g/mol
Molar mass
302.3240g/mol
Density
2.4400g/cm3
Appearence

2,4-dibromo-6-chlorophenol appears as a white to off-white crystalline solid.

Comment on solubility

Solubility of 2,4-Dibromo-6-chloro-phenol

The solubility of 2,4-dibromo-6-chloro-phenol, a halogenated phenolic compound, can be quite intriguing. This compound exhibits different solubility properties depending on the solvent used due to its unique structure and functional groups.

Key Solubility Characteristics:

  • Polar Solvents: 2,4-dibromo-6-chloro-phenol tends to have higher solubility in polar solvents such as water, although the presence of bromine and chlorine substituents can influence its interaction with the solvent.
  • Non-polar Solvents: In contrast, this compound shows increased solubility in non-polar solvents like hexane or toluene, making it ideal for various applications in organic synthesis.
  • Influence of Temperature: The solubility may vary significantly with changes in temperature; generally, an increase in temperature results in increased solubility for solids.

In summary, the solubility of 2,4-dibromo-6-chloro-phenol is affected by:

  1. Nature of the solvent (polar vs. non-polar)
  2. Temperature conditions
  3. Concentration of the compound

Understanding these aspects of solubility not only aids in practical applications but also in predicting the behaviors of such compounds in environmental and biological systems.

Interesting facts

Interesting Facts About 2,4-Dibromo-6-chloro-phenol

2,4-Dibromo-6-chloro-phenol is a fascinating organic compound that belongs to the class of halogenated phenols. This compound is not just notable for its unique chemical structure but also for its various applications and implications in both industrial and environmental settings.

Chemical Characteristics

This compound features two bromine atoms and one chlorine atom attached to the phenolic ring, which significantly influences its reactivity and stability. Some key attributes include:

  • Halogenation: The presence of bromine and chlorine enhances the compound's electrophilic nature, making it useful in various chemical reactions.
  • Functional Diversity: It can serve as a precursor or intermediate in the synthesis of more complex organic molecules.

Applications

2,4-Dibromo-6-chloro-phenol has various practical uses, such as:

  • Antimicrobial Agent: This compound exhibits antibacterial and antifungal properties, making it advantageous in the formulation of antiseptics and disinfectants.
  • Pesticides and Herbicides: It is utilized in agricultural chemistry as an agent to protect crops from pests and unwanted plant growth.

Environmental Impact

Despite its usefulness, the halogenated nature of 2,4-dibromo-6-chloro-phenol raises some environmental concerns:

  • Persistence: The compound tends to be more persistent in the environment, raising questions about bioaccumulation and long-term ecological effects.
  • Toxicity: Care must be taken when handling this substance, as it may pose risks to both human health and wildlife if not managed properly.

In the world of chemistry, 2,4-dibromo-6-chloro-phenol serves as a prime example of how modifications to a simple phenolic structure can lead to varied chemical behavior and applications. As researchers continue to explore this compound, its multifunctionality may reveal further potential that can benefit multiple fields.

Synonyms
4526-56-1
Phenol, 2,4-dibromo-6-chloro-
DTXSID40196456
DTXCID50118947
620-945-8
2,4-Dibromo-6-chlorophenol
6-Chloro-2,4-dibromophenol
MFCD00029692
2-chloro-4,6-dibromophenol
SCHEMBL4644670
MQSIWVCWTVYFDP-UHFFFAOYSA-N
AKOS024336179
AB92883
CS-0452619
NS00132873
E89348