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1,2-Diphenylethane

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Identification
Molecular formula
C14H14
CAS number
103-29-7
IUPAC name
(1-chloro-2-phenyl-ethyl)benzene
State
State

At room temperature, 1,2-Diphenylethane is typically in a liquid state.

Melting point (Celsius)
24.00
Melting point (Kelvin)
297.00
Boiling point (Celsius)
282.00
Boiling point (Kelvin)
555.00
General information
Molecular weight
182.27g/mol
Molar mass
182.2660g/mol
Density
1.0050g/cm3
Appearence

1,2-Diphenylethane appears as a colorless to pale yellow liquid. It is typically clear and may have a faint aromatic odor that is characteristic of compounds containing phenyl groups.

Comment on solubility

Solubility of (1-chloro-2-phenyl-ethyl)benzene

(1-chloro-2-phenyl-ethyl)benzene, with a complex molecular structure, exhibits particular solubility characteristics that are essential for understanding its behavior in different environments. As a **chlorinated aromatic compound**, it tends to be more soluble in organic solvents compared to water. The following points summarize its solubility profile:

  • Solvent Preference: This compound readily dissolves in non-polar solvents such as hexane and toluene, while exhibiting low solubility in polar solvents like water.
  • Effect of Chlorine: The presence of the chlorine atom enhances the compound's polarity slightly, yet it remains predominantly hydrophobic.
  • Temperature Influence: Increased temperatures can improve the solubility of (1-chloro-2-phenyl-ethyl)benzene in organic solvents by overcoming intermolecular forces.
  • Concentration Behavior: As concentration increases, the solubility might plateau due to saturation limits in the chosen solvent.

In summary, the solubility of (1-chloro-2-phenyl-ethyl)benzene is characterized by its affinity towards organic solvents, while its limited solubility in water emphasizes its hydrophobic nature. This knowledge is crucial for its applications in chemical syntheses and various industrial processes.

Interesting facts

Interesting Facts about (1-chloro-2-phenyl-ethyl)benzene

(1-chloro-2-phenyl-ethyl)benzene, a fascinating aromatic compound, is primarily known for its intriguing structure and applications in organic chemistry.

Structure and Properties

This compound features a chlorine atom attached to a secondary carbon in a phenethyl group, which is further connected to a benzene ring. The combination of the aliphatic and aromatic components provides unique properties:

  • Functional Diversity: The presence of the chlorine substituent allows for reactivity and makes it a useful intermediate in organic synthesis.
  • Hydrophobic Character: The aromatic nature contributes to its lipophilicity, making it useful in developing certain materials and chemicals.

Applications

In the field of organic synthesis, (1-chloro-2-phenyl-ethyl)benzene can be used to:

  • Synthesize Pharmaceuticals: It serves as a precursor for various pharmaceuticals, allowing chemists to build complex molecular frameworks.
  • Produce Functional Materials: Its reactivity enables the formation of polymers and materials with specific properties tailored for industrial needs.

Cultural Relevance

This compound may not be in the limelight, but its utility is well-recognized in many scientific communities. As a chemistry student, one might appreciate the way this compound exemplifies the beauty and functionality in the complex world of organic chemistry.

In the words of a famous chemist: “The most exciting thing about chemistry is that it allows us to participate in the creation of new materials that can change our lives.” This sentiment reflects the significance of compounds like (1-chloro-2-phenyl-ethyl)benzene in driving innovation forward.


Synonyms
(2-chloro-2-phenylethyl)benzene
866-816-1
4714-14-1
(1-chloro-2-phenylethyl)benzene
1,2-Diphenyl chloroethane
NSC93
1-chloro-1,2-diphenylethane
2-chloro-1,2-diphenylethane
.ALPHA.-CHLORODIBENZYL
SCHEMBL253443
NSC 93
NSC-93
1,2-DIPHENYLCHLOROETHANE
UVROAJFELBNMRA-UHFFFAOYSA-N
EAA71414
AKOS002663181
DS-008232
CS-0262243
EN300-81869
G49555