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2-Methyl-2,5-dihydrothiophene 1,1-dioxide

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Identification
Molecular formula
C5H8O2S
CAS number
96-73-1
IUPAC name
2-methyl-2,5-dihydrothiophene 1,1-dioxide
State
State

The compound is typically found as a colorless liquid at room temperature.

Melting point (Celsius)
-54.00
Melting point (Kelvin)
219.15
Boiling point (Celsius)
244.50
Boiling point (Kelvin)
517.65
General information
Molecular weight
120.18g/mol
Molar mass
122.1710g/mol
Density
1.1960g/cm3
Appearence

This compound is a colorless liquid at room temperature. It may have a slight characteristic odor.

Comment on solubility

Solubility of 2-methyl-2,5-dihydrothiophene 1,1-dioxide

2-methyl-2,5-dihydrothiophene 1,1-dioxide, a compound containing a thiophene ring, exhibits unique solubility characteristics that are primarily influenced by its molecular structure. Generally, compounds like this one are most likely to be soluble in:

  • Polar solvents: Due to the presence of the sulfur atom and the sulfone functional group, which promotes interaction with polar molecules.
  • Organic solvents: Such as ethanol, methanol, or acetone, commonly used for compounds with similar structures.

However, it is important to note that the solubility can vary significantly depending on several factors:

  • Temperature: Increased temperatures can lead to higher solubility.
  • pH level: Changes in pH can affect ionic interactions and thus impact solubility.
  • Presence of other solutes: The introduction of different solutes can create competitive environments that modify solubility.

In summary, while 2-methyl-2,5-dihydrothiophene 1,1-dioxide is soluble in various solvents, its solubility profile remains a compound of interest that combines both practical applications and intriguing chemical behavior.

Interesting facts

Interesting Facts about 2-methyl-2,5-dihydrothiophene 1,1-dioxide

2-methyl-2,5-dihydrothiophene 1,1-dioxide is a fascinating heterocyclic compound that belongs to the class of thiophene derivatives. Its unique structure and properties make it a subject of interest in various fields of chemistry.

Key Properties and Uses:

  • Versatile Building Block: This compound serves as an important building block in organic synthesis, especially in the development of pharmaceuticals and agrochemicals.
  • Electrophilic Character: The presence of the sulfone group contributes to its electrophilic properties, making it useful in various chemical reactions.
  • Odoriferous Nature: Compounds similar to thiophene are known for their distinct odors, which play a vital role in the fragrance industry.

Chemical Reactivity:

The reactivity of 2-methyl-2,5-dihydrothiophene 1,1-dioxide can be attributed to:

  • Its ability to undergo electrophilic substitution reactions, providing a pathway for synthesizing more complex molecules.
  • Formation of various derivatives that can possess differing physical and biological properties, allowing for tailored applications.

Research Potential:

Researchers are increasingly intrigued by this compound for several reasons:

  • Design of New Materials: Its unique electronic properties make it a potential candidate for the development of novel materials, including conductive polymers.
  • Biological Investigations: Initial studies suggest that derivatives of this compound may exhibit interesting biological activities, prompting further exploration.

In conclusion, 2-methyl-2,5-dihydrothiophene 1,1-dioxide is more than just a simple chemical compound. Its diverse applications and the ongoing research into its properties underscore its significance in the world of chemistry. As scientists continue to uncover its potential, we can expect to see exciting advancements stemming from this intriguing molecule!

Synonyms
6007-71-2
2-methyl-2,5-dihydrothiophene 1,1-dioxide
THIOPHENE, 2,5-DIHYDRO-2-METHYL-, 1,1-DIOXIDE
2,5-Dihydro-2-methylthiophene 1,1-dioxide
2-Methylsulfolene
2-Methylsulfol-3-ene
BRN 0110050
methylsulfolene
4-17-00-00153 (Beilstein Handbook Reference)
SCHEMBL5074223
DTXSID50975496
STL454383
AKOS002275006
2,5-Dihydro-2-methyl-thiophene 1,1-dioxide
2-Methyl-2,5-dihydro-1H-1lambda~6~-thiophene-1,1-dione