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Bis(4-chlorophenyl)methanol

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Identification
Molecular formula
C13H10Cl2O
CAS number
90-23-3
IUPAC name
bis(4-chlorophenyl)methanol
State
State

At room temperature, bis(4-chlorophenyl)methanol is in a solid state.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
357.00
Boiling point (Kelvin)
630.15
General information
Molecular weight
253.13g/mol
Molar mass
253.1260g/mol
Density
1.2750g/cm3
Appearence

Bis(4-chlorophenyl)methanol appears as a white crystalline solid. It is typically in powder form and may have a faint aromatic odor.

Comment on solubility

Solubility of Bis(4-Chlorophenyl)methanol

Bis(4-chlorophenyl)methanol, a compound characterized by its interesting structural attributes, exhibits notable solubility behaviors in various solvents. Understanding the solubility of this compound is essential, as it plays a crucial role in its applications and interactions.

Key Solubility Insights:

  • Polar Solvents: Bis(4-chlorophenyl)methanol demonstrates enhanced solubility in polar solvents such as water and alcohols. The presence of the hydroxyl group (-OH) significantly contributes to its dissolution capabilities.
  • Non-Polar Solvents: Comparatively, the compound shows limited solubility in non-polar solvents. This behavior can be attributed to the lack of significant donor-acceptor interactions that facilitate solvation in such environments.
  • Temperature Influence: Solubility is often temperature-dependent. An increase in temperature generally leads to increased solubility of bis(4-chlorophenyl)methanol, as higher thermal energy assists in overcoming intermolecular forces.
  • Concentration Effects: Upon careful adjustment of concentration, variations in solubility are observed, and this is particularly important in reactions involving this compound.

As stated, "the solubility of a compound can dictate its usability and applicability." Therefore, understanding the solubility of bis(4-chlorophenyl)methanol is paramount for researchers and practitioners who seek to exploit its unique properties in various applications.

Interesting facts

Interesting Facts about Bis(4-chlorophenyl)methanol

Bis(4-chlorophenyl)methanol is a fascinating compound that belongs to the category of organic chemicals. Here are some engaging aspects of this compound:

  • Structure and Composition: The compound features a central carbon atom bonded to two 4-chlorophenyl groups and a hydroxyl group. This unique structure contributes to its reactivity and interactions in various chemical processes.
  • Applications: Bis(4-chlorophenyl)methanol has garnered interest in the fields of pharmaceuticals and agrochemicals. Its derivatives are often investigated for potential use in antimicrobial and anti-inflammatory applications.
  • Toxicology Studies: Due to its chlorinated structure, it is critical to study the toxicity and environmental impact of bis(4-chlorophenyl)methanol. Research has shown that chlorinated compounds can exhibit different biological activities, making safety assessments essential.
  • Synthesis Routes: Scientists have developed various synthesis methods to create bis(4-chlorophenyl)methanol, including direct chlorination procedures and alkylation reactions. These methods symbolize the intricate nature of organic synthesis.
  • Research Opportunities: Given its interesting properties, bis(4-chlorophenyl)methanol serves as an excellent candidate for further studies. Researchers are keen on exploring its potential for novel applications in drug development and other fields.

In summary, bis(4-chlorophenyl)methanol is much more than just a compound; it represents a world of opportunities for innovation and discovery in chemistry. As scientists continue to unravel its secrets, we may witness exciting advancements in various industries!

Synonyms
4,4'-Dichlorobenzhydrol
90-97-1
Bis(4-chlorophenyl)methanol
P,P'-DICHLOROBENZHYDROL
4,4-dichlorobenzhydrol
4,4'-Dichlorodiphenylcarbinol
CR5KH591G4
4,4'-dichlorobenzhydryl alcohol
4,4'-Dichloro-alpha-phenylbenzylic alcohol
p,p'-DCBH
NSC-5250
EINECS 202-029-6
Benzenemethanol, 4-chloro-a-(4-chlorophenyl)-
MFCD00000629
bis(p-chlorophenyl)methanol
NSC 121779
NSC-121779
UNII-CR5KH591G4
Benzenemethanol, 4-chloro-.alpha.-(4-chlorophenyl)-
AI3-05090
DTXSID5075367
Methanol, bis-(p-chlorophenyl)-
CHEBI:190399
Benzenemethanol, 4-chloro-alpha-(4-chlorophenyl)-
BENZHYDROL, 4,4'-DICHLORO-
Bis(4-chlorophenyl--d4)Methyl Alcohol
4-chloro-alpha-(4-chlorophenyl)benzenemethanol
4,4 inverted exclamation marka-Dichlorobenzhydrol
4-CHLORO-.ALPHA.-(4-CHLOROPHENYL)BENZENEMETHANOL
4,4/'-Dichlorobenzhydrol
NSC5250
4,4\'-Dichlorobenzhydrol
Bis(4-chlorophenyl) carbinol
bis(4-chlorophenyl)-methanol
Bis(4-chlorophenyl)methanol #
bis-(4-Chlorophenyl)-carbinol
SCHEMBL1426754
DTXCID9048699
diphenylcarbinol, 4,4'-dichloro-
NSC121779
AKOS009031548
AC-10402
BS-42459
FC137993
4-Chloro-a-(4-chlorophenyl)benzenemethanol
DB-057233
D1915
NS00039381
EN300-20367
D89943
Q27894524
Z104477892