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1,2-dichloro-3-phenoxybenzene

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Identification
Molecular formula
C12H8Cl2O
CAS number
7698-88-6
IUPAC name
1,2-dichloro-3-phenoxy-benzene
State
State

At room temperature, 1,2-dichloro-3-phenoxybenzene is in a solid state, but it can transition to a liquid at temperatures above its melting point.

Melting point (Celsius)
34.00
Melting point (Kelvin)
307.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
237.09g/mol
Molar mass
237.0860g/mol
Density
1.3563g/cm3
Appearence

1,2-Dichloro-3-phenoxybenzene typically appears as a colorless to pale yellow liquid. It may exhibit a slightly aromatic odor due to its structural components.

Comment on solubility

Solubility of 1,2-Dichloro-3-phenoxy-benzene

1,2-Dichloro-3-phenoxy-benzene, often referred to for its unique chemical structure, exhibits interesting solubility characteristics worth noting:

  • Solvent Compatibility: This compound is generally more soluble in organic solvents compared to water, largely due to its hydrophobic aromatic and chlorinated structures.
  • Polarity Considerations: The presence of chlorine atoms increases its molecular weight and affects its polarity, making it less soluble in polar solvents like water.
  • Temperature Effects: Solubility can vary with temperature; typically, increased temperatures can enhance the solubility in organic solvents.
  • Environmental Impact: Understanding its solubility is crucial in environmental chemistry, as its behavior in various solvents can influence its mobility and bioavailability in ecosystems.

In conclusion, while 1,2-Dichloro-3-phenoxy-benzene is less soluble in polar solvents, it demonstrates enhanced solubility in non-polar organic solvents. As a result, it is important to choose appropriate solvents for various applications and analyses.

Interesting facts

Interesting Facts About 1,2-Dichloro-3-phenoxy-benzene

1,2-Dichloro-3-phenoxy-benzene, often referred to by its common names in various chemical discussions, is an intriguing compound known for its unique structural characteristics and applications. Here are some fascinating insights into this compound:

  • Structure and Reactivity: The presence of both chlorine and phenoxy groups in the compound significantly influences its chemical reactivity, making it an exciting subject for chemists. The dichloro substitution pattern can lead to unique pathways in chemical synthesis.
  • Applications: This compound is utilized in various industrial applications, particularly in the production of herbicides. Its effectiveness in targeting specific plant growth pathways makes it valuable in agricultural chemistry.
  • Environmental Impact: Due to its chlorine content, studies have been conducted to assess its environmental consequences. Understanding the degradation pathways of this compound is crucial, as it helps in evaluating the potential effects on ecosystems and human health.
  • Research Significance: Researchers are interested in 1,2-dichloro-3-phenoxy-benzene for its potential in synthesizing more complex organic molecules. The compound serves as a versatile intermediate in the field of organic synthesis.
  • Biological Activity: Some derivatives of this compound have been studied for their biological activity, contributing to the field of pharmaceuticals by providing insights into potential therapeutic applications.

In conclusion, 1,2-dichloro-3-phenoxy-benzene is not only a compound of industrial significance but also a subject of research that helps expand our understanding of chlorinated aromatic compounds. As chemists continue to explore its properties, we can expect new discoveries that will further illuminate its versatility and applications.

Synonyms
2,3-Dichlorodiphenyl ether
UNII-8W2LZ352CC
8W2LZ352CC
Benzene, 1,2-dichloro-3-phenoxy-
68486-28-2
PCDE 5
DTXSID3074026
RefChem:81609
DTXCID2037847
28675-08-3
1,2-dichloro-3-phenoxybenzene
Benzene, 1,1'-oxybis-, dichloro deriv.
Dichloro diphenyl ether
Ether, dichlorophenyl
Phenyl ether dichloro
Dichloro diphenyl oxide
UNII-TBM8LLJ0UH
PHENYL ETHER DIEHLORO
AI3-01203
TBM8LLJ0UH
Benzene, 1,1'-oxybis-, dichloro derivative
SCHEMBL2533671
SCHEMBL2533674
SCHEMBL2750692
SCHEMBL2752869
SCHEMBL3667279
2,3-dichloro-1-phenoxy-benzene
VSKSUBSGORDMQX-UHFFFAOYSA-N
Q27271102