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Methylethylsulfonate

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Identification
Molecular formula
C3H6O3S
CAS number
1142-67-4
IUPAC name
4-methyl-1,3,2-dioxathiolane 2-oxide
State
State

At room temperature, Methylethylsulfonate is a liquid. Its colorless to pale yellow appearance is typical for many organosulfur compounds.

Melting point (Celsius)
-52.00
Melting point (Kelvin)
221.15
Boiling point (Celsius)
84.00
Boiling point (Kelvin)
357.15
General information
Molecular weight
122.16g/mol
Molar mass
122.1630g/mol
Density
1.2610g/cm3
Appearence

4-methyl-1,3,2-dioxathiolane 2-oxide, commonly known as Methylethylsulfonate, typically appears as a colorless to pale yellow liquid. Its clear nature allows for easy handling in laboratories.

Comment on solubility

Solubility of 4-methyl-1,3,2-dioxathiolane 2-oxide

The solubility of 4-methyl-1,3,2-dioxathiolane 2-oxide presents an interesting profile due to its unique molecular structure. This compound is known to be:

  • Soluble in polar solvents: Its ability to interact with polar molecules allows it to dissolve readily in solvents such as water and alcohol.
  • Insoluble in non-polar solvents: On the contrary, the presence of sulfur and oxygen atoms contributes to its aversion to non-polar solvents like hexane.
  • Reactive in solution: When dissolved, it can participate in chemical reactions that may further affect its solubility.

As a general observation, the solubility of organic compounds such as this one is largely influenced by factors including:

  1. Functional groups: The presence of electronegative atoms like sulfur and oxygen increases polarity.
  2. Molecular size: The size and hydrophobic character of the compound also play crucial roles.
  3. Temperature: Increased temperatures often lead to higher solubility for many organic compounds.

In conclusion, the solubility behavior of 4-methyl-1,3,2-dioxathiolane 2-oxide is primarily dictated by its polar characteristics, allowing it to be utilized effectively in various aqueous environments, while limiting its applications in non-polar settings. Understanding these attributes is essential for its applications in chemical synthesis and reactivity.

Interesting facts

Interesting Facts about 4-Methyl-1,3,2-dioxathiolane 2-oxide

4-Methyl-1,3,2-dioxathiolane 2-oxide is a fascinating compound with unique properties that make it noteworthy in the world of chemistry. Here are some interesting highlights about this compound:

  • Structure and Composition: This compound features a five-membered cyclic structure that includes both sulfur and oxygen atoms. The presence of the dioxathiolane structure adds intriguing elements to its reactivity.
  • Reactivity: As a 1,3-dioxathiolane, it is known for its ability to undergo various transformations, making it valuable in organic synthesis. Compounds of this type are often used as intermediates in chemical reactions.
  • Applications: 4-Methyl-1,3,2-dioxathiolane 2-oxide has potential applications in the synthesis of pharmaceuticals and agrochemicals. Its reactive nature can be harnessed in creating more complex molecular architectures.
  • Environmental Considerations: Understanding the behavior of compounds like 4-methyl-1,3,2-dioxathiolane 2-oxide in the environment is critical. Research into its ecological impact is essential for sustainable chemical practices.

Scientists are particularly interested in the properties of such dioxathiolanes due to their roles in the formation of various functional groups in organic chemistry. As one researcher aptly put it, "The beauty of chemistry lies in its ability to transform simple elements into complex structures that define our world."

Overall, this compound represents the intricate dance of atoms and bonds, showcasing the multifaceted nature of chemical compounds. Its study continues to inspire future research and innovation in diverse fields.

Synonyms
1469-73-4
Propylene sulfite
1,2-Propanediol sulfite
AI3-22919
SULFUROUS ACID, CYCLIC ESTER with 1,2-PROPANEDIOL
sjhayvfvkrxmkg-uhfffaoysa-n
4-Methyl-1,3,2-dioxathiolane 2-oxide
1,3,2-Dioxathiolane, 4-methyl-, 2-oxide
Cyclic propylene sulfite
Propane-1,2-cyclic sulfite
1,2-Propylene glycol sulfite
Propylene sulfite (C3H6O2)SO
Sulfurous acid, cyclic propylene ester
1,2-Propanediol, cyclic sulfite
NSC 44145
NSC 525703
4-METHYL-1,3,2??-DIOXATHIOLAN-2-ONE
40811-14-1
1,2-Propyleneglycol Sulfite
WLN: T6OSOTJ BO
Sulfurous acid,2-propanediol
1,3,2-Dioxathiolane, 4-methyl-, 2-oxide, trans-
Propane 1,2-Cyclic Sulfite
1,2-Dioxathiolane, 4-methyl-, 2-oxide
MFCD00041209
4-Methyl-1,3,2-dioxathiolane2-oxide
1,2-propylene sulfite
SCHEMBL126716
1,2-Propanediol Cyclic Sulfite
CHEMBL1980710
DTXSID80932956
NSC44145
NSC-44145
NSC525703
AKOS006273771
1,2-Propyleneglycol sulfite, >=98%
NSC-525703
AS-64052
NCI60_004285
4-Methyl-1,3,2-dioxathiolane 2-oxide #
DB-241968
M2471
(4R)-4-methyl-1,3,2-dioxathiolane 2-oxide
(4S)-4-methyl-1,3,2-dioxathiolane 2-oxide
4-Methyl-1,3,2lambda~4~-dioxathiolan-2-one
D91602
1006381-02-7
221370-80-5