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2,2-bis(ethylsulfonyl)butane

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Identification
Molecular formula
C8H18O4S2
CAS number
6065-31-4
IUPAC name
2,2-bis(ethylsulfonyl)butane
State
State

At room temperature, 2,2-bis(ethylsulfonyl)butane is a solid. The compound is stable under normal conditions and should be stored in a cool, dry place. It may remain stable without significant decomposition when handled and stored correctly.

Melting point (Celsius)
60.00
Melting point (Kelvin)
333.15
Boiling point (Celsius)
307.00
Boiling point (Kelvin)
580.15
General information
Molecular weight
182.28g/mol
Molar mass
182.2840g/mol
Density
1.1897g/cm3
Appearence

2,2-bis(ethylsulfonyl)butane is typically found in the form of a white to off-white crystalline solid. Its crystalline nature may contribute to a granular or powdery texture. The compound's appearance may vary slightly depending on purity and processing methods.

Comment on solubility

Solubility of 2,2-bis(ethylsulfonyl)butane

The solubility of 2,2-bis(ethylsulfonyl)butane can exhibit interesting characteristics due to its unique chemical structure. This compound, with its ethylsulfonyl functional groups, interacts with solvents in fascinating ways. Here, we will explore its solubility behavior:

  • Polar Solvents: 2,2-bis(ethylsulfonyl)butane is likely to show better solubility in polar solvents due to the presence of the sulfonyl groups, which can engage in hydrogen bonding and dipole-dipole interactions.
  • Non-Polar Solvents: In contrast, the solubility in non-polar solvents may be limited, as the non-polar regions of the butane backbone do not favorably interact with such solvents.
  • Water Solubility: Although the compound contains polar groups, the relatively large hydrophobic butane chain may hinder its solubility in water, making it moderately soluble at best.

Some general observations about the solubility of similar compounds suggest that:

  1. Application Specificity: The solubility can vary greatly depending on the specific application or use-case scenario for which the compound is intended.
  2. Temperature Dependence: Solubility might also be influenced by changes in temperature, which can affect molecular interactions.

In summary, while 2,2-bis(ethylsulfonyl)butane displays certain solubility trends, the degree to which it dissolves will largely depend on both the choice of solvent and environmental conditions. Its characteristic sulfonyl groups play a crucial role in interaction with potential solvent molecules, highlighting the intricate relationship between structure and solubility.

Interesting facts

Interesting Facts About 2,2-bis(ethylsulfonyl)butane

2,2-bis(ethylsulfonyl)butane is a fascinating compound due to its unique structure and potential applications in various fields. Here are some intriguing aspects of this compound:

  • Functional Groups: This compound contains sulfonyl groups, which are known for their ability to enhance the reactivity of organic compounds. The presence of these groups makes 2,2-bis(ethylsulfonyl)butane an interesting subject for further chemical research.
  • Synthesis: The synthesis of 2,2-bis(ethylsulfonyl)butane can provide insights into organic synthesis techniques. Scientists often explore different pathways to create such compounds, and understanding its synthesis may lead to the development of more efficient chemical processes.
  • Potential Applications: The structural features of this compound may have implications in fields like pharmaceuticals, where sulfonyl groups are often involved in drug design. Compounds that include sulfonyl functional groups can exhibit unique biological activities, making them valuable in medicinal chemistry.
  • Chemical Stability: 2,2-bis(ethylsulfonyl)butane's stability under different conditions can offer valuable information regarding its potential uses. The stability of organic compounds under heat and other reactive conditions is highly relevant for industrial applications.

As a compound rich in functional groups and with numerous potential applications, 2,2-bis(ethylsulfonyl)butane continues to pique the interest of chemists and researchers alike. Its unique properties serve as a reminder of the complexity and diversity found within organic chemistry.

In the words of renowned chemist Linus Pauling: "The best way to have a good idea is to have a lot of ideas." Exploring compounds like 2,2-bis(ethylsulfonyl)butane is a perfect way to spark creativity and innovation in the fields of science and chemistry.

Synonyms
Sulfonethylmethane
Methylsulfonal
2,2-Bis(ethylsulfonyl)butane
TRIONAL
Methylsulphonal
Trionalon
Metilosulfonal
76-20-0
Sulfonethylmethanum
Diethylsulfonmethylethylmethane
Methylsulfonalum
2,2-Bis(ethylsulphonyl)butane
Sulphonethylmethane
Sulfonethylmethane [NF]
NSC 3994
NSC-3994
EINECS 200-942-4
BRN 1785184
DTXSID7046411
Butane, 2,2-bis(ethylsulfonyl)-
UNII-217727W28W
Tional
SULFONETHYLMETHANE [MI]
METHYLSULFONAL [WHO-DD]
217727W28W
DTXCID5026411
NSC3994
3-01-00-02790 (Beilstein Handbook Reference)
NCGC00164518-01
Ethylsulfonal
DEA No. 2605
t i o n a l
SCHEMBL5624
Butane,2-bis(ethylsulfonyl)-
CHEMBL1990189
Butane,2,2-bis(ethylsulfonyl)-
CHEBI:134987
LKACJLUUJRMGFK-UHFFFAOYSA-N
WLN: WS2&X2&1&SW2
Tox21_112153
AKOS003245042
CAS-76-20-0
DS-007311
NS00037763
Q7843147
200-942-4