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1,2,2-Triphenylethanol

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Identification
Molecular formula
C20H18O
CAS number
3774-15-0
IUPAC name
1,2,2-triphenylethanol
State
State

At room temperature, 1,2,2-Triphenylethanol is in a solid state.

Melting point (Celsius)
161.00
Melting point (Kelvin)
434.15
Boiling point (Celsius)
382.00
Boiling point (Kelvin)
655.15
General information
Molecular weight
274.35g/mol
Molar mass
274.3510g/mol
Density
1.0550g/cm3
Appearence

1,2,2-Triphenylethanol is a colorless solid. Its crystalline form can be described as powdery or in the form of small, clear crystals.

Comment on solubility

Solubility of 1,2,2-Triphenylethanol

1,2,2-Triphenylethanol, with the chemical formula C18H18O, exhibits interesting solubility characteristics due to its unique structural composition. This compound consists of a central ethanol unit flanked by three phenyl groups, which significantly influence its solubility profile.

When considering the solubility of 1,2,2-triphenylethanol, it's essential to note the following factors:

  • Solubility in Organic Solvents: 1,2,2-Triphenylethanol is generally more soluble in organic solvents such as ethanol and benzene. This is primarily due to its non-polar phenyl groups, which favor interactions with similar non-polar environments.
  • Limited Solubility in Water: Conversely, this compound has limited solubility in water. The hydrophobic nature of the phenyl groups limits the ability of the molecule to interact favorably with polar water molecules.
  • Temperature Influence: As with many organic compounds, solubility can be affected by temperature; increasing temperature may enhance solubility in certain organic solvents.

In summary, while 1,2,2-triphenylethanol is well-soluble in non-polar media, it finds itself poorly soluble in polar solvent systems. This dual behavior exemplifies the importance of understanding molecular structure in predicting solubility characteristics.

Interesting facts

Interesting Facts about 1,2,2-Triphenylethanol

1,2,2-Triphenylethanol is a fascinating compound that stands out in the world of organic chemistry due to its unique structure and properties. This compound is often utilized in various applications, displaying a combination of chemical stability and reactivity that is particularly interesting for chemical research and industrial processes.

Key Characteristics

  • Chirality: 1,2,2-Triphenylethanol is a chiral molecule, which means it exists in two enantiomeric forms. This aspect makes it a significant compound in the field of stereochemistry.
  • Intermediate in Synthesis: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals and agrochemicals, showcasing its versatility in organic synthesis.
  • Functional Groups: The presence of hydroxyl (–OH) groups in its structure provides the compound with the ability to engage in hydrogen bonding, influencing its reactivity and interaction with other substances.

Applications

1,2,2-Triphenylethanol finds its applications in numerous fields:

  • Pharmaceuticals: It is often employed in the synthesis of various drugs due to its ability to impart specific properties to the resultant compounds.
  • Chemical Research: Its unique properties make it a subject of interest in organic chemistry research, particularly for studies related to stereochemistry and reaction mechanisms.
  • Materials Science: Researchers are exploring the potential of 1,2,2-triphenylethanol in modifying materials and creating new compounds with desirable properties.

Did You Know?

The synthesis of 1,2,2-triphenylethanol often involves the use of specific catalysts and can be linked to significant discoveries in organic chemistry. As Dr. Robert H. Grubbs once said, “Chemistry is not just about the molecules; it’s about the transformations they undergo.” 1,2,2-Triphenylethanol exemplifies this notion by demonstrating how a simple compound can lead to complex and vital applications.

In conclusion, 1,2,2-triphenylethanol is not just another organic compound; it serves as an essential tool in various scientific realms and showcases the intricate relationships between molecular structure and function.

Synonyms
1,2,2-Triphenylethanol
2294-93-1
DTXSID90274672
DTXCID30226135
vnqnlcdogbokpl-uhfffaoysa-n
Benzyldiphenylmethanol
alpha-Benzylbenzhydrol
1,2,2-Triphenylethan-1-ol
Benzhydrol, alpha-benzyl-
Ethanol, 1,1,2-triphenyl-
1-Hydroxy-1,1,2-triphenylethane
EINECS 224-614-5
alpha,alpha-Diphenylphenethyl alcohol
Benzeneethanol, alpha,alpha-diphenyl-
NSC 56476
BRN 2053575
Phenethyl alcohol, alpha,alpha-diphenyl-
starbld0028418
SCHEMBL26608146
4-06-00-05057 (Beilstein Handbook Reference)