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5-Methylsulfonyloxypentyl methanesulfonate

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Identification
Molecular formula
C7H16O6S2
CAS number
4724-47-2
IUPAC name
5-methylsulfonyloxypentyl methanesulfonate
State
State

This compound is typically in a liquid state at room temperature, with a slightly oily texture.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
293.00
Boiling point (Kelvin)
566.15
General information
Molecular weight
244.32g/mol
Molar mass
244.3230g/mol
Density
1.4053g/cm3
Appearence

5-Methylsulfonyloxypentyl methanesulfonate appears as a colorless to pale yellow liquid. It may also be found in impure forms as a slightly turbid solution.

Comment on solubility

Solubility of 5-methylsulfonyloxypentyl methanesulfonate

5-methylsulfonyloxypentyl methanesulfonate is a compound that exhibits interesting solubility characteristics depending on environmental conditions. Generally, its solubility can be influenced by several factors:

  • Polarity: The presence of sulfonate groups makes the compound relatively polar, which typically enhances solubility in polar solvents such as water.
  • Temperature: Like many chemical compounds, solubility often increases with temperature. Thus, higher temperatures may lead to a greater degree of solubility in aqueous solutions.
  • pH Levels: The solubility of this compound can also be affected by the pH of the solution. In acidic or basic environments, the behavior of the sulfonate groups may change, impacting solubility.
  • Solvent Choice: While it shows better solubility in water, using organic solvents might result in varied solubility levels; hence, knowing the solvent's nature is crucial.

In summary, the solubility of 5-methylsulfonyloxypentyl methanesulfonate is generally favorable in polar solvents, particularly water, but is also dependent on specific environmental conditions. As stated, "Understand your solvent, to understand your solubility!"

Interesting facts

Interesting Facts about 5-methylsulfonyloxypentyl methanesulfonate

5-methylsulfonyloxypentyl methanesulfonate, often abbreviated as 5-MSPMS, is a fascinating compound that belongs to the class of organosulfonates. This compound is particularly interesting for several reasons:

  • Chemical Structure: 5-MSPMS features a unique combination of pentyl and methanesulfonate groups. The **methylsulfonyl** functional group enhances its reactivity and versatility in various chemical reactions.
  • Use in Synthesis: It serves as a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The presence of sulfonate groups often imparts enhanced solubility and facilitates chemical transformations.
  • Green Chemistry: The inclusion of 5-MSPMS in chemical reactions aligns with the principles of green chemistry, as sulfones generally exhibit lower toxicity and are less hazardous than their halogenated counterparts.
  • Applications: Its applications extend to various fields including medicinal chemistry, where it may be involved in synthesizing biologically active compounds, and materials science, where it could be employed in the development of functional polymers.
  • Stability: The compound is characterized by its stability under a variety of conditions, a property that is critical for its use in industrial applications and pharmaceutical formulations.
  • Research Potential: Ongoing research is investigating the optimization of 5-MSPMS in different chemical pathways, including potential uses that may not yet be fully explored, making it a compound to watch in future studies.

Overall, 5-methylsulfonyloxypentyl methanesulfonate stands out not only for its functional capabilities but also as an exemplary case of modern advancements in organic synthesis and green practices in chemistry. It truly embodies the innovative spirit at the heart of scientific endeavors.

Synonyms
1,5-Dimesyloxypentane
2374-22-3
1,5-Pentanediol dimethanesulfonate
5-methylsulfonyloxypentyl methanesulfonate
NSC 17019
1,5-PENTANEDIOL, DIMETHANESULFONATE
1,5-Pentanediol bis(methanesulfonate)
BRN 1794833
AI3-51905
pentane-1,5-diyl dimethanesulfonate
1,5-dimethanesulfonyloxypentane
SCHEMBL1335477
DTXSID00178410
1,5-bis(methanesulfonyloxy)pentane
1,5-Pentanediol dimethanesulphonate
NSC17019
NSC-17019
DS-020990
5-[(Methylsulfonyl)oxy]pentyl methanesulfonate
5-[(Methylsulfonyl)oxy]pentyl methanesulfonate #