Skip to main content

2,3,5-Tribromophenol

ADVERTISEMENT
Identification
Molecular formula
C6H3Br3O
CAS number
14620-08-1
IUPAC name
2,3,5-tribromophenol
State
State

At room temperature, 2,3,5-Tribromophenol is a solid. Its stability as a solid compound makes it manageable in various synthesis processes and ensures consistency in its phenolic properties.

Melting point (Celsius)
92.00
Melting point (Kelvin)
365.00
Boiling point (Celsius)
288.00
Boiling point (Kelvin)
561.00
General information
Molecular weight
330.83g/mol
Molar mass
330.8280g/mol
Density
2.7990g/cm3
Appearence

2,3,5-Tribromophenol appears as a white to off-white crystalline solid. It is often noted for its brominated aromatic ring structure that can contribute to its pale coloration. This compound is used in organic synthesis and can have a strong, phenolic odor.

Comment on solubility

Solubility of 2,3,5-Tribromophenol

2,3,5-Tribromophenol, with the chemical formula C6H3Br3O, exhibits interesting solubility characteristics due to its structure and the presence of bromine atoms. This compound is primarily known for its behavior in different solvents, which can be summarized as follows:

  • In Water: 2,3,5-Tribromophenol has limited solubility in water. The numerous bromine substituents hinder its ability to interact favorably with water molecules.
  • In Organic Solvents: Conversely, it is more soluble in organic solvents such as ethanol and acetone. This is attributed to the hydrophobic nature of the bromine groups, which enhances interactions with non-polar solvents.
  • In Acidic Solutions: The solubility can increase in acidic conditions, as protons can interact with the compound, forming a more soluble ionic form.

Overall, the solubility behavior of 2,3,5-tribromophenol emphasizes the importance of the chemical environment influencing its dissolution properties. As stated, "The greater the complexity of structure, the more nuanced the solubility." This compound serves as a great example of how substituents and intermolecular interactions dictate solubility dynamics.

Interesting facts

Interesting Facts About 2,3,5-Tribromophenol

2,3,5-Tribromophenol is a fascinating compound with a variety of applications and interesting characteristics that make it significant in the field of chemistry. Below are some key points about this compound:

  • Structure and Composition: This compound features a phenolic structure, meaning it is based on a benzene ring with hydroxyl (-OH) group, modified by three bromine atoms. The positioning of these bromines at the 2, 3, and 5 positions creates a unique trifunctional molecular compound.
  • Antimicrobial Properties: 2,3,5-Tribromophenol is known for its broad-spectrum antimicrobial activity. Research has shown it can effectively inhibit the growth of various bacteria and fungi, which makes it valuable in medical and industrial applications.
  • Application in Pesticides: This compound often plays a crucial role in the formulation of agricultural pesticides and herbicides. Its ability to disrupt biological processes in organisms contributes to its effectiveness as an agricultural chemical.
  • Impact on the Environment: Due to its bromine content, 2,3,5-tribromophenol can have substantial environmental implications. It is important to monitor and manage its use to minimize potential ecological harm, as halogenated compounds can be persistent in the environment.
  • Historical Significance: The study of phenolic compounds has a rich history within organic chemistry, and 2,3,5-tribromophenol represents an evolution in the synthesis and application of these substances over time.

Overall, 2,3,5-tribromophenol is not just another chemical compound; it is a junction of applications across various fields such as agriculture, pharmaceuticals, and environmental science. Understanding its properties and implications allows chemists and researchers to better navigate its uses and impacts, echoing the saying, “With great power comes great responsibility” when dealing with such potent substances.


Synonyms
2,3,5-tribromophenol
Phenol, 2,3,5-tribromo-
57383-81-0
SCHEMBL591287
SCHEMBL12816770
SKDJCHZVXDLVIE-UHFFFAOYSA-N