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1-vinylsulfonylethylene

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Identification
Molecular formula
C4H6O2S
CAS number
1113-79-3
IUPAC name
1-vinylsulfonylethylene
State
State

At room temperature, 1-vinylsulfonylethylene is in a liquid state due to its relatively low melting point and moderate boiling point.

Melting point (Celsius)
-19.00
Melting point (Kelvin)
254.15
Boiling point (Celsius)
222.00
Boiling point (Kelvin)
495.15
General information
Molecular weight
136.19g/mol
Molar mass
136.1880g/mol
Density
1.2540g/cm3
Appearence

1-Vinylsulfonylethylene presents as a clear, colorless to light yellow liquid. It tends to have a slightly pungent odor, characteristic of many organic sulfone compounds.

Comment on solubility

Solubility of 1-Vinylsulfonylethylene

1-Vinylsulfonylethylene, with its unique sulfonyl functional group, presents interesting solubility characteristics. This compound is generally known to be moderately soluble in polar solvents, such as water, due to the presence of the sulfonic acid group, which can engage in hydrogen bonding and dipole-dipole interactions.

Key points regarding the solubility of 1-vinylsulfonylethylene include:

  • Polar Solvents: It shows a greater affinity for polar solvents owing to its polar functional groups.
  • Hydrophobic Environment: The compound may experience reduced solubility in non-polar solvents, as the vinyl group contributes to hydrophobic characteristics.
  • Concentration Effects: At higher concentrations, the solubility may be influenced by factors such as temperature and ionic strength.

In summary, while 1-vinylsulfonylethylene has a beneficial solubility profile in polar media, its behavior can vary significantly in different environments—an important factor to consider in practical applications.

Interesting facts

Interesting Facts About 1-Vinylsulfonylethylene

1-Vinylsulfonylethylene, a fascinating compound within the realm of organic chemistry, holds significant potential for various applications due to its unique structural features and reactivity. Here are some interesting highlights:

  • Versatile Building Block: This compound serves as a vital intermediate in the synthesis of polymers and other complex molecules. Its vinyl group can participate in various reactions, making it a versatile building block in organic synthesis.
  • Unique Functionalities: The sulfonyl group present in this compound imparts distinctive chemical properties, enhancing its reactivity. This can lead to the formation of sulfonates, which are useful in further chemical transformations.
  • Applications in Material Science: Due to its ability to polymerize, 1-vinylsulfonylethylene is explored in creating advanced materials, including hydrogels and specialty coatings. Such materials can exhibit improved durability and functionality, making them valuable in various industrial applications.
  • Contribution to Medicinal Chemistry: Compounds like 1-vinylsulfonylethylene are also investigated in pharmaceutical research. The modifications of this compound may lead to the discovery of new drug candidates with enhanced biological activity.
  • Reactivity with Functional Groups: The presence of multiple functional groups allows this compound to interact with a range of other reagents, offering opportunities for innovative synthetic pathways and reaction strategies.

As a chemist or a student, delving into the world of 1-vinylsulfonylethylene can spark exciting discussions about reactivity, polymer science, and the future of chemical synthesis. With its versatile nature and implications in both materials science and medicinal chemistry, this compound embodies the creativity and ingenuity that drives the field of chemistry forward.

Synonyms
Divinyl sulfone
VINYL SULFONE
77-77-0
Divinyl sulphone
Bis(ethenyl)sulfone
vinyl sulphone
Ethenesulfonyl-ethene
Sulfone, divinyl-
Ethene, 1,1'-sulfonylbis-
1,1'-Sulphonylbisethene
(ethenesulfonyl)ethene
Ethene,1,1'-sulfonylbis-
divinylsulfone
1-ethenylsulfonylethene
vinylsulfonylethene
(CH2=CH)2SO2
1-(Vinylsulfonyl)ethylene
1-vinylsulfonylethylene
TL 797
vinylsulfone
1,1'-sulfonyldiethene
CCRIS 4349
CHEBI:53729
HSDB 2028
UNII-5PFN71LP8M
EINECS 201-057-6
NSC 18590
BRN 1071329
(ethenylsulfonyl)ethene
AI3-26598
1,1'-sulfonyldiethylene
MFCD00008623
NSC-18590
NSC-57304
ETHENYLSULFONYLETHENE
NSC-133793
5PFN71LP8M
VINYL SULFONE [HSDB]
DTXSID6031253
Ethene,1'-sulfonylbis-
Divinyl Sulfone (Stabilized with Hydroquinone)
WLN: 1U1SW1U1
Diethenyl sulphone
62804-37-9
(vinylsulfonyl)ethene
Vinyl sulfone (8CI)
SULFONE, DIVINYL
Ethene, 1,1'sulfonylbis
Epitope ID:116218
SCHEMBL23101
1-(Vinylsulfonyl)ethylene #
CHEMBL349205
1,1'-SULFONYLBISETHANE
DTXCID4011253
NSC18590
NSC57304
STR02154
BBL027719
NSC133793
STL373436
AKOS009156703
AT13126
DIVINYL SULFONE, STABILIZED WITH HQ
D0959
NS00022784
EN300-36195
A23558
Q27104812
Divinyl sulfone, 97%, stab. with 0.05% hydroquinone
F8889-6525
Z362768182
Divinyl sulfone, contains <650 ppm hydroquinone as inhibitor, 97%
1,3,2-Dioxaphospholane, 2-chloro-;1,3,2-Dioxaphosphorane.2-chloro-;Ethylenephosphorochloridite