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4-phenylbenzene-1,2-diol

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Identification
Molecular formula
C12H10O2
CAS number
2131-57-7
IUPAC name
4-phenylbenzene-1,2-diol
State
State

At room temperature, 4-phenylbenzene-1,2-diol is typically in a solid state. The compound is crystalline in structure, indicating a well-defined geometric arrangement of atoms.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
158.17g/mol
Molar mass
158.1730g/mol
Density
1.2400g/cm3
Appearence

4-Phenylbenzene-1,2-diol, also known as 4-phenylcatechol, typically appears as a white to off-white crystalline powder. Its precise appearance may vary depending on its purity and the conditions under which it is observed.

Comment on solubility

Solubility of 4-phenylbenzene-1,2-diol

4-phenylbenzene-1,2-diol, also known as 4-phenylcatechol, exhibits interesting solubility properties that can vary based on several factors. Understanding its solubility can aid in applications across various fields. Here are some key points regarding its solubility:

  • Polar vs. Nonpolar: 4-phenylbenzene-1,2-diol contains both aromatic rings and hydroxyl groups, which contribute to its solubility behavior. The presence of hydroxyl groups typically increases solubility in polar solvents, while the nonpolar aromatic rings may enhance solubility in nonpolar solvents.
  • Water Solubility: Due to the two hydroxyl groups, this compound is expected to have moderate solubility in water, allowing for hydrogen bonding with water molecules.
  • Solubility in Organic Solvents: This compound is likely to be less soluble in highly polar solvents and more soluble in organic solvents like ethanol, acetone, or dichloromethane, given its hydrophobic character from the phenyl groups.
  • Temperature Influence: Solubility can also be affected by temperature; increasing the temperature may enhance the solubility of the 4-phenylbenzene-1,2-diol in various solvents.

In summary, the solubility of 4-phenylbenzene-1,2-diol showcases a fascinating balance between its polar and nonpolar characteristics. It serves as a reminder of the intricate nature of solubility, where “like dissolves like” often applies, but the nuances of molecular structure must be taken into account for precise predictions.

Interesting facts

Interesting Facts about 4-phenylbenzene-1,2-diol

4-phenylbenzene-1,2-diol, also known as 4-phenylcatechol, exhibits fascinating properties and plays a significant role in various fields of research and application. Here are some intriguing aspects of this compound:

  • Structure and Isomerism: This compound features a unique structure where a phenyl group is located at the 4-position of the benzene ring, and two hydroxyl groups are situated at the 1 and 2 positions. This positional isomerism leads to distinct physical and chemical properties.
  • Biological Relevance: 4-phenylbenzene-1,2-diol has been studied for its potential biological activities. For instance, its catechol moiety can engage in redox reactions, which makes it interesting for exploring antioxidant properties.
  • Applications in Organic Synthesis: This compound serves as a crucial building block in organic synthesis, particularly in the synthesis of larger, more complex aromatic compounds. Its functional groups can be utilized for further modifications.
  • Environmental Impact: Some studies suggest that derivatives of catechol are used in the development of new drug delivery systems and environmentally friendly pesticides, highlighting the compound's role in sustainable chemistry.
  • Research Focus: Recent research has focused on the development of catalysts involving 4-phenylbenzene-1,2-diol, making it a topic of interest in catalytic studies, especially for complex organic reactions.

The functionalities of 4-phenylbenzene-1,2-diol and its derivatives exemplify how **aromatic compounds** with hydroxyl groups can lead to diverse chemical pathways and applications. As research progresses, it will be exciting to see how scientists harness the properties of this compound in innovative ways.

Synonyms
[1,1'-Biphenyl]-3,4-diol
3,4-Biphenyldiol
92-05-7
4-PHENYLCATECHOL
4-Phenylpyrocatechol
3,4-Dihydroxybiphenyl
Biphenyl-3,4-diol
4-phenylbenzene-1,2-diol
4-Phenyl-1,2-benzenediol
3.4-Biphenyldiol
1,2-Benzenediol, 4-phenyl-
(1,1'-Biphenyl)-3,4-diol
T7L7XJ8RU1
1,1'-Biphenyl-3,4-Diol
NSC 1267
NSC-1267
EINECS 202-121-6
4,5-DIHYDROXYBIPHENYL
AI3-17381
CHEMBL475398
DTXSID0059039
PYROCATECHOL, 4-PHENYL-
UNII-T7L7XJ8RU1
4mmm
NSC1267
BP7
MFCD00041746
[1,4-diol
Biphenyl, 3,4-dihydroxy
Cambridge id 5510868
Oprea1_102735
SCHEMBL928289
DTXCID2048745
QDNPCYCBQFHNJC-UHFFFAOYSA-
HMS1581P06
BDBM50624921
AKOS006275086
DB07478
PD005150
CS-0235672
NS00039430
Y10998
EN300-1599483
Q27096697
Z1198148367
InChI=1/C12H10O2/c13-11-7-6-10(8-12(11)14)9-4-2-1-3-5-9/h1-8,13-14H