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2-(Methylsulfonyloxy)ethyl methanesulfonate

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Identification
Molecular formula
C4H10O6S2
CAS number
32970-85-1
IUPAC name
2-methylsulfonyloxyethyl methanesulfonate
State
State

This compound is typically found as a liquid at room temperature.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
333.00
Boiling point (Kelvin)
606.15
General information
Molecular weight
216.25g/mol
Molar mass
216.2500g/mol
Density
1.4200g/cm3
Appearence

2-(Methylsulfonyloxy)ethyl methanesulfonate is typically a colorless liquid. It is not commonly encountered in solid state and usually appears as a clear or slightly yellowish liquid.

Comment on solubility

Solubility of 2-methylsulfonyloxyethyl methanesulfonate

2-methylsulfonyloxyethyl methanesulfonate is a fascinating compound with notable solubility properties. Understanding the solubility of this compound can be quite enriching, especially when considering its potential applications. Here are some key points regarding its solubility:

  • Polarity: Due to the presence of sulfonate groups, this compound displays significant polar characteristics, typically leading to high solubility in polar solvents.
  • Solvents: It tends to dissolve well in water and other polar solvents, which enhances its utility in various chemical processes.
  • Influencing Factors: Solubility can be affected by factors such as temperature, pH, and the presence of other solutes. For instance, increasing temperature generally increases the solubility of many compounds.
  • Applications: The solubility in different media allows for its use in various applications ranging from organic synthesis to potential pharmaceutical formulations.

In summary, the solubility of 2-methylsulfonyloxyethyl methanesulfonate is highly dependent on its structural features and the solvent environment, making it an intriguing compound for further exploration.

Interesting facts

Interesting Facts about 2-Methylsulfonyloxyethyl Methanesulfonate

2-Methylsulfonyloxyethyl methanesulfonate is a fascinating compound in the realm of chemical synthesis and organic chemistry. Known for its versatility, this compound can be utilized in various applications, making it an interesting subject for both chemists and researchers alike.

Key Applications

  • Reagent in Synthesis: It serves as an important reagent in chemical synthesis, particularly in the production of sulfonate esters.
  • Medicinal Chemistry: The compound has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals.
  • Functional Group Manipulation: Its unique structure allows for the modification of functional groups in other organic compounds.

Chemical Properties and Reactivity

This compound is notably reactive due to the sulfonate group, making it particularly useful in nucleophilic substitution reactions. Its ability to undergo various chemical transformations is of great interest in the synthesis of more complex organic molecules.

Fun Facts

  • Some chemists refer to compounds with sulfonate groups as having "sulfonyl magic" due to their reactivity and usefulness in synthetic routes.
  • The synthesis of 2-methylsulfonyloxyethyl methanesulfonate often involves multistep processes, showcasing the intricate planning involved in organic synthesis.

As research continues, the potential uses and properties of 2-methylsulfonyloxyethyl methanesulfonate may lead to breakthroughs in various fields of chemistry. Its role as a versatile and effective building block underscores the importance of studying such compounds in a scientific context.

Synonyms
Ethylene dimethanesulfonate
4672-49-5
Ethane dimethanesulphonate
Ethylene methanesulfonate
Ethylene glycol dimesylate
Ethane dimethane sulphonate
Dimethylene dimethanesulfonate
Ethane 1,2-dimethanesulfonate
Ethylene dimethanesulphonate
1,2-Ethanediol dimethanesulfonate
1,2-Ethanediol, dimethanesulfonate
ethane dimethanesulfonate
ETHYLENE GLYCOL, DIMETHANESULFONATE
Methanesulfonic acid, ethylene ester
NC 429
NSC 10716
ethane dimethane sulfonate
1,2-Ethanediyl methanesulfonate
Ethylene-1,2-dimethanesulphonate
Ethylene glycol dimethanesulfonate
1,2-Ethanediol, bismethanesulfonate
Ethylene-1,2-dimethanesulfonate
UNII-EW8V7BJ66Q
NSC 17016
BRN 1787642
AI3-61167
1,2-Ethanediol dimethanesulphonate
NSC-17016
1,2-ethanediol, 1,2-dimethanesulfonate
DTXSID40196931
1,2-Ethylene bis(methanesulfonate)
Ethane-1,2-diol dimethanesulphonate
ETHYLENE GLYCOL BIS(METHANESULFONATE)
Methanesulfonic acid 2-methanesulfonyloxy-ethyl ester
ethane dimethyl sulfonate
ethanediol 1,2-dimethanesulfonate
DTXCID80119422
1,2-Ethanediol, dimethanesulfonate (9CI)
4-04-00-00019 (beilstein handbook reference)
qsqfarngnizgaw-uhfffaoysa-n
1,2-Bis(mesyloxy)ethane
DMSE
Ethylene bis(methanesulfonate)
1,2-Ethanediyl dimethanesulfonate
2-methylsulfonyloxyethyl methanesulfonate
2-(methanesulfonyloxy)ethyl methanesulfonate
1,2-bis(methanesulfonyloxy)ethane
52410-74-9
ethylene dimethane sulfonate
EDS
POLYETHYLENE GLYCOL 4000 DIMESYLATE
MFCD00025060
EW8V7BJ66Q
CHEMBL170630
SCHEMBL1336145
1,2-bis-methanesulfonyloxy-ethane
NSC17016
AKOS034019861
AS-75637
DA-53044
SY155250
2-(methanesulfonyloxy)ethylmethanesulfonate
HY-129524
CS-0106333
EN300-137131
F20584
2-[(Methylsulfonyl)oxy]ethyl methanesulfonate #
Q27277396
Z1269115552