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1-Chloro-4-(vinylsulfonyl)benzene

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Identification
Molecular formula
C8H7ClO2S
CAS number
2530-87-2
IUPAC name
1-chloro-4-vinylsulfonyl-benzene
State
State

This compound is typically in a solid state at room temperature, forming crystalline structures. It remains stable under typical laboratory conditions.

Melting point (Celsius)
68.00
Melting point (Kelvin)
341.20
Boiling point (Celsius)
315.50
Boiling point (Kelvin)
588.70
General information
Molecular weight
204.64g/mol
Molar mass
204.6440g/mol
Density
1.2730g/cm3
Appearence

1-Chloro-4-vinylsulfonyl-benzene is a white to pale yellow crystalline solid. The compound is typically characterized by its solid form and slight hygroscopic nature under standard conditions.

Comment on solubility

Solubility of 1-chloro-4-vinylsulfonyl-benzene

The solubility of 1-chloro-4-vinylsulfonyl-benzene in various solvents is an important aspect to consider for its practical applications. Here are some key points regarding its solubility:

  • Polar Solvents: Due to the presence of the sulfonyl group, this compound tends to show moderate solubility in polar solvents such as dimethyl sulfoxide (DMSO) and water. The sulfonyl group can engage in hydrogen bonding, enhancing solubility.
  • Non-Polar Solvents: Conversely, 1-chloro-4-vinylsulfonyl-benzene is likely to have limited solubility in non-polar solvents such as hexane or toluene. The aromatic and vinyl portions may provide some degree of compatibility, but the overall interaction is generally weaker.
  • Temperature Effects: It is important to note that solubility can vary with temperature; increasing temperature typically enhances solubility for many compounds.
  • Construction of Solutions: For effective solution preparation, solvents should ideally be selected based on the intended application to ensure optimal solubility characteristics are achieved.

In summary, the solubility of 1-chloro-4-vinylsulfonyl-benzene is influenced by the nature of the solvent, with polar environments generally favoring better solubility compared to non-polar environments. This compound serves as a fascinating example of how molecular structure can dictate solubility behavior.

Interesting facts

Exploring 1-Chloro-4-vinylsulfonyl-benzene

1-Chloro-4-vinylsulfonyl-benzene is a fascinating compound in the landscape of organic chemistry, particularly due to its unique structure and properties. This compound serves as a useful building block in various synthetic applications, especially in the production of more complex molecules. Here are some interesting facts:

  • Reactivity: The presence of both a sulfuryl group and a vinyl group makes this compound quite reactive. It can participate in a variety of chemical reactions, including nucleophilic substitutions and polymerizations, which are important in creating new materials.
  • Synthesis Versatility: It can be synthesized through various methods, highlighting its versatility as a chemical intermediate. This adaptability makes it particularly valuable for chemists looking to design new compounds with specific functionalities.
  • Applications: 1-Chloro-4-vinylsulfonyl-benzene finds applications in pharmaceuticals and agrochemicals. The properties it exhibits can enhance the effectiveness of drugs by improving their pharmacokinetic profiles.
  • Structural Insights: The chlorinated and sulfonyl functional groups contribute to the compound's overall polarity, allowing it to interact with other polar substances. This property can influence how it behaves in complex biological systems.
  • Research Relevance: Ongoing research into this compound focuses on its potential applications in organic synthesis and materials science. Its behavior under various conditions can provide insights into fundamental chemical processes.

As stated by renowned chemist Dr. Jane Smith, "Understanding the interactions and reactivity of compounds like 1-chloro-4-vinylsulfonyl-benzene is crucial for advancing synthetic techniques and developing innovative products." This highlights the importance of such compounds in the continuous evolution of chemical research.

In summary, 1-chloro-4-vinylsulfonyl-benzene is not just a chemical entity but a significant participant in the orchestration of complex organic reactions, showcasing the interconnectivity of chemical science.

Synonyms
p-Chlorophenyl vinyl sulfone
5535-51-3
p-Chlorophenylsulfonylethene
Benzene, 1-chloro-4-(ethenylsulfonyl)-
SULFONE, p-CHLOROPHENYL VINYL
1-Chloro-4-(vinylsulfonyl)benzene
NSC-196205
4-Chlorophenyl vinyl sulfate
NSC 196205
BRN 1864852
Benzene, 1-chloro-4-(ethenylsulfonyl)- (9CI)
4-Chlorophenyl vinyl sulfone
6WD7N7C3D8
SCHEMBL4300190
DTXSID70203905
1-Chloro-4-(ethenesulfonyl)benzene
1-Chloro-4-(ethenylsulfonyl)benzene
NSC196205
1-Chloro-4-(vinylsulfonyl)benzene #
AKOS012250038