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1-Chloro-4-(1-chlorovinyl)cyclohexene

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Identification
Molecular formula
C8H10Cl2
CAS number
989-06-4
IUPAC name
1-chloro-4-(1-chlorovinyl)cyclohexene
State
State

At room temperature, 1-chloro-4-(1-chlorovinyl)cyclohexene is a liquid.

Melting point (Celsius)
-25.00
Melting point (Kelvin)
248.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
174.08g/mol
Molar mass
174.0810g/mol
Density
1.0490g/cm3
Appearence

1-Chloro-4-(1-chlorovinyl)cyclohexene is typically a colorless liquid with a mild odor. It can become slightly yellow upon exposure to light or air.

Comment on solubility

Solubility of 1-chloro-4-(1-chlorovinyl)cyclohexene

1-chloro-4-(1-chlorovinyl)cyclohexene is an interesting compound when it comes to solubility, largely due to its unique structure and the presence of chlorine atoms. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound demonstrates moderate solubility in organic solvents such as hexane and ethanol, but it is generally insoluble in water.
  • Influence of Chlorine: The presence of chlorine substitutions often results in increased polarity, which impacts its solubility behavior.
  • Effect of Temperature: Solubility may increase with rising temperatures, which can facilitate interactions between the compound and solvent molecules.

As a compound that exhibits varying degrees of solubility depending on the solvent and conditions, it is essential to consider these factors when predicting its behavior in different chemical contexts. The solubility characteristics can greatly affect its applications in chemical reactions and synthesis.

Interesting facts

Interesting Facts about 1-chloro-4-(1-chlorovinyl)cyclohexene

1-chloro-4-(1-chlorovinyl)cyclohexene, a fascinating organic compound, belongs to the family of chlorinated cycloalkenes. Here are several key points that highlight its significance:

  • Structure and Chirality: This compound features a cyclohexene ring, making it part of the cyclic hydrocarbons. Its structural intricacy provides chiral centers, which are of great interest in asymmetric synthesis and in the development of pharmaceuticals.
  • Reactivity: The presence of multiple chlorine atoms introduces unique reactivity patterns, making it a valuable intermediate in organic synthesis. Chlorinated compounds often participate in various reactions, including nucleophilic substitutions and eliminations.
  • Applications: Beyond being a synthetic intermediate, compounds with similar structures are often researched for their potential application in agriculture as pesticides or herbicides. The chlorovinyl group may enhance the biological activity of certain derivatives.
  • Environmental Impact: Like many halogenated compounds, 1-chloro-4-(1-chlorovinyl)cyclohexene must be handled with care. This also invites research into environmental chemistry to understand its degradation pathways and ecological effects.
  • Historical Significance: The study of chlorinated hydrocarbons burgeoned in the mid-20th century, spurred on by the development of synthetic organic chemistry. Compounds like this played a critical role in understanding reaction mechanisms and assembling complex molecules.

In summary, 1-chloro-4-(1-chlorovinyl)cyclohexene offers a unique glimpse into the intricate world of organic compounds, with its interesting structure, diverse applications, and implications for both chemistry and environmental science.

Synonyms
13547-06-3
Cyclohexene, 1-chloro-4-(1-chloroethenyl)-
1-CHLORO-4-(1-CHLOROETHENYL)CYCLOHEXENE
1-CHLORO-4-(1-CHLOROETHENYL)-CYCLOHEXENE
Cyclohexene, 1-chloro-4-(1-chlorovinyl)-
Cyclohexene, 1-chloro-4-(1-chlorophenyl)-
SCHEMBL16860576
DTXSID10929016
1-chloro-4-(1-chlorovinyl)-cyclohexene
1-Chloro-4-(.alpha.-chlorovinyl)cyclohexene
1-Chloro-4-(1-chlorovinyl)-1-cyclohexene #
1-CHLORO-4-(1-CHLOROETHENYL)CYCLOHEX-1-ENE