Skip to main content

Dichloro(phenyl)methanol

ADVERTISEMENT
Identification
Molecular formula
C7H6Cl2O
CAS number
101-02-0
IUPAC name
dichloro(phenyl)methanol
State
State

At room temperature, dichloro(phenyl)methanol is a solid.

Melting point (Celsius)
60.00
Melting point (Kelvin)
333.20
Boiling point (Celsius)
295.40
Boiling point (Kelvin)
568.50
General information
Molecular weight
176.02g/mol
Molar mass
176.0210g/mol
Density
1.3970g/cm3
Appearence

This chemical compound is a crystalline solid. It is typically white in color and has a distinct aromatic odor associated with its phenyl group.

Comment on solubility

Solubility of Dichloro(phenyl)methanol

Dichloro(phenyl)methanol, with the chemical formula C7H6Cl2O, exhibits unique solubility characteristics that are influenced by its molecular structure. This compound is known to be:

  • Partially soluble in water: Due to the presence of the hydroxyl (-OH) group, dichloro(phenyl)methanol can engage in hydrogen bonding with water molecules, enhancing its solubility. However, the chlorinated substituents may impede complete dissolution.
  • Soluble in organic solvents: It shows good solubility in organic solvents such as ethanol, acetone, and chloroform. This strong solubility in non-polar or less polar environments is typical for compounds with significant hydrophobic character.

In summary, the solubility of dichloro(phenyl)methanol can be attributed to its dual nature:

  1. Hydrophilic due to the -OH group, allowing interaction with water.
  2. Hydrophobic due to the phenyl and chloro substituents, which favor solubility in organic matrices.

As the famous chemist Linus Pauling once noted, "The character of a molecule is its solubility." Understanding the solubility behavior of dichloro(phenyl)methanol provides valuable insight into its potential applications and chemical interactions.

Interesting facts

Interesting Facts about Dichloro(phenyl)methanol

Dichloro(phenyl)methanol is a fascinating compound that has intrigued scientists due to its unique structure and reactivity. Here are some engaging aspects to consider:

  • Structural Significance: The presence of both chlorine and phenyl groups in its structure makes dichloro(phenyl)methanol noteworthy for exploring electron-withdrawing effects, affecting its reactivity.
  • Application in Organic Synthesis: This compound is often used as an intermediate in the synthesis of various organic molecules, including pharmaceuticals and agrochemicals, showcasing its versatility in chemical reactions.
  • Environmental Considerations: Like many chlorinated compounds, it raises environmental concerns due to its potential reactivity and persistence in the ecosystem. Understanding its behavior and degradation pathways is crucial for environmental chemistry.
  • Research and Safety: In laboratory settings, researchers must handle dichloro(phenyl)methanol with care, as it can pose health risks if not managed properly, sparking discussions on chemical safety protocols.
  • Analytical Techniques: This compound can be analyzed using various spectral techniques such as NMR and IR, offering insights into its structural properties and functional groups, making it a valuable subject in analytical chemistry.

In conclusion, dichloro(phenyl)methanol is not just another chemical compound; its multifaceted applications, structural uniqueness, and critical role in environmental discussions make it a compelling subject for further study in the world of chemistry. As chemists continue to investigate its properties, we gain deeper insights into functional organic compounds.

Synonyms
Benzenemethanol, dichloro-
BENZYL ALCOHOL, DICHLORO-
dichloro(phenyl)methanol
12041-76-8
Dichlorobenzenemethanol
SCHEMBL456764
SCHEMBL1831719
SCHEMBL9257902
SCHEMBL20486905