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(1-methyl-4-methylsulfonyloxy-pentyl) methanesulfonate

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Identification
Molecular formula
C8H18O6S2
IUPAC name
(1-methyl-4-methylsulfonyloxy-pentyl) methanesulfonate
State
State
This compound is typically a liquid at room temperature, and it may be hygroscopic.
Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.15
General information
Molecular weight
252.35g/mol
Molar mass
252.3500g/mol
Density
1.2900g/cm3
Appearence

The compound is typically in a liquid state at room temperature, with a clear to slightly yellow appearance. It may have a slight odor due to its sulfonate groups.

Comment on solubility

Solubility of (1-methyl-4-methylsulfonyloxy-pentyl) methanesulfonate

The solubility characteristics of (1-methyl-4-methylsulfonyloxy-pentyl) methanesulfonate (C8H18O6S2) may be quite intriguing due to its complex structure. Solubility is greatly influenced by several factors:

  • Polarity: Given the presence of sulfonate groups, the compound is expected to exhibit significant polarity, enhancing its solubility in polar solvents such as water.
  • Hydrogen Bonding: The functional groups can participate in hydrogen bonding, further promoting solubility in aqueous solutions.
  • Hydrophobic Regions: The hydrocarbon portions of the molecule can introduce hydrophobic characteristics, potentially affecting its solubility in non-polar solvents.

Overall, it can be stated that:

  1. The compound is likely soluble in polar solvents.
  2. Inefficient solubility may occur in non-polar environments.

In conclusion, the solubility of (1-methyl-4-methylsulfonyloxy-pentyl) methanesulfonate is predicted to be moderately high in water, assisting in applications that require effective dissolution and reactivity.

Interesting facts

Interesting Facts about (1-methyl-4-methylsulfonyloxy-pentyl) methanesulfonate

(1-methyl-4-methylsulfonyloxy-pentyl) methanesulfonate is a compound that presents intriguing characteristics, making it a topic of interest in the field of organic chemistry. Here are some compelling points about this compound:

  • Versatile Applications: This compound may find use in various applications such as pharmaceuticals, agricultural chemicals, and as a reagent in organic synthesis due to the presence of both a sulfonyl and an alkyl group.
  • Mechanism of Action: Compounds like this often involve interesting mechanisms when interacting with biological systems, making them valuable for drug development.
  • Synthetic Pathways: As a sulfonate ester, it can be synthesized through several methods, often involving nucleophilic substitution. This opens doors for showcasing advanced synthesis techniques in educational settings.
  • Environmental Impact: As with many sulfonate compounds, understanding their environmental behavior is essential, especially in terms of biodegradability and potential toxicity.
  • Chemical Reactivity: The presence of the methanesulfonate group can enhance electrophilic reactivity, allowing for further chemical modifications, leading to the development of diverse derivatives.

In the realm of medicinal chemistry, compounds similar to (1-methyl-4-methylsulfonyloxy-pentyl) methanesulfonate are often utilized as prodrugs. As stated by many researchers, “Prodrugs are strategically designed to improve drug solubility and bioavailability.” This highlights the potential of such sulfonate esters in advancing therapeutic options.

Overall, studying (1-methyl-4-methylsulfonyloxy-pentyl) methanesulfonate can deepen our understanding of functional groups and their impact on molecular behavior, providing valuable insights into both synthetic strategies and real-world applications.

Synonyms
Dimethylmyleran
Dimethylbusulfan
55-93-6
2,5-Dimethanesulfomyloxyhexane
hexane-2,5-diyl dimethanesulfonate
1,4-dimethylmyleran
1,4-dimethylbusulfan
1,4-Dimethanesulfonoxy-1,4-dimethylbutane
OS 22
5-methylsulfonyloxyhexan-2-yl methanesulfonate
1,4-Bis(methylsulfonyloxy)-1,4-dimethylbutane
NSC-23890
2,5-hexanediol dimesylate
CB 2348
DMM
2,5-hexanediol dimethylsulfonate
1,4-dimethylbutane
2, dimethylsulfonate
2,5-Hexanediol, dimethanesulfonate (7CI,8CI,9CI)
2, dimethanesulfonate
WLN: WS1&OY1&2Y1&OSW1
NSC 23890
2,5-Hexanediol, dimethanesulfonate, (-)-
Methanesulfonic acid,4-dimethyltetramethylene ester
33447-91-5
(+)-Dimethylmyleran
(-)-Dimethylmyleran
NSC 180541
Dimethylmyleran, meso-
2,5-HEXANEDIOL, DIMETHYLSULFONATE
AI3-50858
2, dimethanesulfonate, meso-
2, dimethanesulfonate, (-)-
Methanesulfonic acid, 1,4-dimethyltetramethylene ester
SCHEMBL2756235
NIOSH/MO2350000
NIOSH/MO2360000
CHEBI:67107
DTXSID601339464
2,5-Hexanediol, dimethanesulfonate
NSC23890
2, dimethanesulfonate, (R*,S*)-
NSC180541
NSC180542
NSC180543
NSC232201
NSC232202
AKOS030532174
NSC-180541
NSC-180542
NSC-180543
NSC-232201
NSC-232202
2, dimethanesulfonate, (R*,R*)-(-)-
2,5-Hexanediol, dimethanesulfonate, (+)-
MO23500000
MO23600000
2, dimethanesulfonate, (R*,R*)-(.+-.)-
Q27135624