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2-Bromo-4,6-dichlorophenol

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Identification
Molecular formula
C6H3BrCl2O
CAS number
839-12-7
IUPAC name
2-bromo-4,6-dichloro-phenol
State
State

2-Bromo-4,6-dichlorophenol is a solid at room temperature.

Melting point (Celsius)
68.00
Melting point (Kelvin)
341.00
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.00
General information
Molecular weight
255.36g/mol
Molar mass
255.3600g/mol
Density
1.9500g/cm3
Appearence

2-Bromo-4,6-dichlorophenol is typically a solid at room temperature. It appears as a crystalline compound and can vary in color from off-white to pale brown.

Comment on solubility

Solubility of 2-bromo-4,6-dichloro-phenol

2-bromo-4,6-dichloro-phenol, with the chemical formula C6H4BrCl2O, exhibits interesting solubility characteristics that are influenced by its halogenated and hydroxyl functional groups.

In terms of solubility:

  • Water Solubility: This compound is generally considered to be moderately soluble in water. Its solubility may be influenced by the presence of the hydroxyl (-OH) group, which can form hydrogen bonds with water molecules.
  • Organic Solvents: 2-bromo-4,6-dichloro-phenol typically shows greater solubility in organic solvents such as ethanol and acetone. This characteristic can be attributed to the non-polar nature of the bromine and chlorine substituents, which enhances compatibility with organic media.
  • Temperature Influence: As with many organic compounds, an increase in temperature generally leads to an increase in solubility in polar solvents like water and various organic solvents.

Overall, the solubility profile of 2-bromo-4,6-dichloro-phenol suggests a nuanced landscape affected by multiple factors such as solvent type and temperature. Understanding these solubility properties is essential for applications in chemical synthesis and formulation technologies.

Interesting facts

Interesting Facts about 2-Bromo-4,6-dichloro-phenol

2-Bromo-4,6-dichloro-phenol is a fascinating compound that offers significant insights into both organic chemistry and material science. Commonly employed in various applications, this compound plays a crucial role in the formation of advanced materials and in some analytical chemistry processes.

Key Features:

  • Halogenated Phenol: Being a halogenated phenol, it contains multiple chlorine and bromine substituents on the phenolic ring, which enhances its reactivity.
  • Antimicrobial Properties: Due to its structure, this compound exhibits notable antibacterial and antifungal activity, making it valuable in the formulation of disinfectants and preservatives.
  • Research Applications: Used in various laboratory settings, it serves as a reagent for synthesizing other chemical compounds and studying reaction mechanisms.
  • Structure-Activity Relationship: Scientists often study how the positioning of halogen atoms affects the compound's biological activities and physical properties, contributing to the development of new pharmaceuticals.

As stated by chemists, “The beauty of brominated and chlorinated compounds lies in their capability to manifest unique reactivity patterns that can lead to innovative solutions.”
With its diverse applications and intriguing properties, 2-bromo-4,6-dichloro-phenol remains an important compound in chemical research and industrial applications.

Fun Fact:

The presence of multiple halogen groups not only influences the reactivity but can also significantly change the compound’s properties like stability and solubility, making it an interesting subject of study for advanced students.

Synonyms
2-Bromo-4,6-dichlorophenol
4524-77-0
Phenol, 2-bromo-4,6-dichloro-
6-BROMO-2,4-DICHLOROPHENOL
3R47HFR4HD
EINECS 224-855-6
NSC 99829
NSC-99829
DTXSID50196447
DTXCID60118938
224-855-6
MFCD00474518
2,4-Dichloro-6-bromophenol
NSC99829
UNII-3R47HFR4HD
2-Bromo-4,6-dichloro-phenol
SCHEMBL2417306
EAA52477
STL066606
AKOS000319637
NCGC00340643-01
SY198134
CS-0168507
NS00031509
EN300-212292
AB01332838-02
AN-329/06268011
F3310-0314
Z223656306