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1,2-dichlorovinylbenzene

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Identification
Molecular formula
C8H6Cl2
CAS number
6802-56-0
IUPAC name
1,2-dichlorovinylbenzene
State
State

1,2-dichlorovinylbenzene is typically a liquid at room temperature.

Melting point (Celsius)
-29.50
Melting point (Kelvin)
243.65
Boiling point (Celsius)
239.00
Boiling point (Kelvin)
512.15
General information
Molecular weight
175.05g/mol
Molar mass
175.0510g/mol
Density
1.2270g/cm3
Appearence

This compound typically appears as a colorless to pale yellow liquid.

Comment on solubility

Solubility of 1,2-Dichlorovinylbenzene

1,2-Dichlorovinylbenzene, with its unique molecular structure, presents interesting characteristics regarding its solubility. You may find it useful to consider the following points:

  • Solvent Compatibility: 1,2-Dichlorovinylbenzene is generally soluble in organic solvents such as chloroform, acetone, and benzene, but is poorly soluble in polar solvents like water.
  • Non-polar Nature: The compound's non-polar regions contribute to its increased solubility in non-polar solvents, adhering to the principle of "like dissolves like."
  • Temperature Effects: Elevated temperatures may enhance solubility in organic solvents, allowing for greater dissolution rates.

It’s crucial to note that these solubility properties can have practical implications in various applications. When considering solubility, always refer to specific experimental conditions and solvent choices to achieve the desired outcomes in your chemical processes.

Interesting facts

Interesting Facts About 1,2-Dichlorovinylbenzene

1,2-Dichlorovinylbenzene, often abbreviated as DVCB, is a fascinating compound within the realm of organic chemistry. This compound belongs to the family of vinylbenzenes, which serve as important building blocks in the synthesis of various materials. Here are some intriguing aspects of DVCB:

  • Applications in Chemistry: DVCB is a valued intermediate in the production of several specialized polymers and agrochemicals. Its reactivity allows for the formation of various derivatives, making it versatile in synthetic routes.
  • Environmental Impact: Like many chlorinated compounds, 1,2-dichlorovinylbenzene draws attention for its environmental persistence and potential toxicity. Scientists study its behavior in different ecosystems to understand its effects and develop safer alternatives.
  • Detection and Analysis: DVCB can be detected using techniques such as gas chromatography-mass spectrometry (GC-MS), providing insights into its presence in environmental samples. This makes it a subject of interest in environmental chemistry.
  • Research Significance: Ongoing research focuses on the mechanisms of reactions involving DVCB, contributing to the broader understanding of reaction kinetics and mechanisms in organic synthesis.
  • Diverse Reactions: DVCB participates in a variety of reactions, including nucleophilic substitutions and polymerization processes, showcasing its importance in chemical synthesis.

To quote an insightful chemist: "In the world of synthesis, it's compounds like 1,2-dichlorovinylbenzene that exemplify the beauty of chemical reactivity and adaptability."
Understanding this compound not only enhances our grasp of synthetic chemistry but also lays the groundwork for future innovations in material science and environmental protection.

Synonyms
alpha,beta-Dichlorostyrene
.alpha.,.beta.-Dichlorostyrene
DTXSID8073132