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DDT

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Identification
Molecular formula
C14H9Cl2
CAS number
50-29-3
IUPAC name
(1,2-dichloro-2-phenyl-vinyl)benzene
State
State

At room temperature, DDT is a solid. It is typically encountered in the form of a crystalline powder. The physical state contributes to its application methods and its stability when used as an insecticide.

Melting point (Celsius)
108.50
Melting point (Kelvin)
381.65
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
354.49g/mol
Molar mass
354.4860g/mol
Density
1.6800g/cm3
Appearence

DDT is a white, crystalline solid with no distinct odor. It is known for its chemical stability and resistance to decomposition in the environment, contributing to its persistence. The compound often appears as a fine powder or in large crystals depending on its preparation.

Comment on solubility

Solubility of (1,2-dichloro-2-phenyl-vinyl)benzene

(1,2-dichloro-2-phenyl-vinyl)benzene, known for its aromatic nature, exhibits specific solubility characteristics that are noteworthy. Generally classified as an organic compound, its solubility can be influenced by various factors:

  • Polarity: The presence of chlorine atoms introduces polar characteristics to the molecule. However, the overall structure remains predominantly non-polar due to the extended aromatic rings.
  • Solvent Compatibility: It tends to dissolve well in organic solvents such as hexane or chloroform, while displaying limited solubility in polar solvents like water.
  • Temperature Influence: As with many organic compounds, solubility can increase with temperature, making it easier to dissolve at elevated temperatures.

In summary, one can say that "(1,2-dichloro-2-phenyl-vinyl)benzene is more soluble in non-polar solvents than in polar ones, reflecting its hydrophobic nature." Understanding these solubility traits is essential for its application in various chemical processes.

Interesting facts

Interesting Facts about (1,2-Dichloro-2-phenyl-vinyl)benzene

(1,2-Dichloro-2-phenyl-vinyl)benzene, often referred to in scientific literature as a noteworthy compound in organic synthesis, has several fascinating aspects that capture the attention of chemists. Here are some key points:

  • Structure and Functionality: This compound belongs to a class of compounds known as chlorinated vinyl derivatives. Its structure exhibits unique aspects, with two chlorine atoms positioned at the 1 and 2 positions of the vinyl group, significantly influencing its chemical reactivity.
  • Applications: (1,2-Dichloro-2-phenyl-vinyl)benzene is utilized in various fields, particularly in organic synthesis. It serves as an intermediate in the production of complex organic molecules and is valued in the manufacture of pharmaceuticals and agrochemicals.
  • Reactivity: The presence of chlorinated groups imparts high reactivity, making this compound an attractive target for nucleophilic substitution reactions. Researchers often explore its potential to participate in cross-coupling reactions, providing pathways to construct diverse organic compounds.
  • Impact on Environment: As with many chlorinated compounds, it’s essential to recognize their environmental impact. Understanding how (1,2-Dichloro-2-phenyl-vinyl)benzene behaves in natural systems is crucial for assessing its ecological risks and ensuring safe usage.
  • Research Opportunities: Ongoing research focuses on delving deeper into its reaction mechanisms and exploring safer alternatives to chlorinated compounds in industry, highlighting a trend towards greener chemistry.

In conclusion, (1,2-Dichloro-2-phenyl-vinyl)benzene stands as a valuable entity in the field of organic chemistry. As scientists continue to investigate its properties and applications, it remains a compound worthy of further exploration and understanding.

Synonyms
13700-82-8
alpha,alpha'-dichlorostilbene
660-652-2
dichlorodiphenylethylene
DTXSID20871815
1,2-Dichloro-1,2-diphenylethene
1,1'-[(E)-1,2-Dichloroethene-1,2-diyl]dibenzene