Skip to main content

Fluorosulfonyloxymethane

ADVERTISEMENT
Identification
Molecular formula
CH3OSO2F
CAS number
677-19-0
IUPAC name
fluorosulfonyloxymethane
State
State

At room temperature, fluorosulfonyloxymethane exists as a liquid. This compound is notable for its relatively stable liquid state compared to other analogous compounds that might be gaseous at room temperature. It remains stable under standard conditions without excessive evaporation or sublimation.

Melting point (Celsius)
-110.00
Melting point (Kelvin)
163.15
Boiling point (Celsius)
85.00
Boiling point (Kelvin)
358.15
General information
Molecular weight
130.09g/mol
Molar mass
130.0880g/mol
Density
1.8636g/cm3
Appearence

Fluorosulfonyloxymethane is a colorless liquid. As with many fluorinated compounds, it may exhibit a characteristic odor associated with sulfur compounds, but specific descriptions of its odor are not detailed in literature. In its pure form, it has a clear appearance without any suspended particles or coloration.

Comment on solubility

Solubility of Fluorosulfonyloxymethane

Fluorosulfonyloxymethane, with the chemical formula FSO2OCH3, exhibits some interesting solubility characteristics.

Typically, the solubility of compounds like fluorosulfonyloxymethane can be influenced by several factors:

  • Polarity: The presence of sulfonyl and oxygen functional groups suggests a polar nature, which generally enhances solubility in polar solvents.
  • Hydrogen Bonding: The potential for hydrogen bonding due to the oxy group can improve interactions with solvents capable of similar hydrogen bonding.
  • Molecular Size: As a relatively small molecule, fluorosulfonyloxymethane may have better solubility in organic solvents compared to larger counterparts.
  • Temperature: Solubility may also vary with temperature, often increasing at higher temperatures.

In summary, fluorosulfonyloxymethane is likely soluble in polar organic solvents due to its polar functional groups and small size. However, comprehensive solubility data in various solvents would enhance our understanding of its behavior in practical applications.

Interesting facts

Interesting Facts About Fluorosulfonyloxymethane

Fluorosulfonyloxymethane is a fascinating compound with unique properties and applications that make it stand out in the world of chemistry. Here are some intriguing aspects to explore:

  • Reactivity: This compound is known for its highly reactive nature. Its fluorosulfanyl group can participate in various chemical reactions, making it a key player in organic synthesis.
  • Applications: Fluorosulfonyloxymethane plays a significant role in the production of fluorinated compounds, which have widespread use in pharmaceuticals, agrochemicals, and materials science.
  • Functional Group: The presence of both the fluorosulfonyloxy and methoxy functional groups creates an interesting synergy, allowing for manipulation of chemical reactivity and selectivity.
  • Safety Considerations: Like many fluorinated compounds, it requires careful handling due to its potential hazards, making safety precautions essential when working with it in a laboratory setting.

Through its reactivity and versatility, fluorosulfonyloxymethane exemplifies the rich complexity of modern chemistry. Its contributions to science highlight the importance of studying unique compounds that offer innovative solutions across various fields. As we continue to delve deeper into the properties of such compounds, we can uncover even more unexpected applications and behavior.

In conclusion, understanding fluorosulfonyloxymethane not only enhances our grasp of organic chemistry but also broadens our perspective on how diverse chemical compounds can influence advancements in technology and industry.

Synonyms
METHYL FLUOROSULFONATE
421-20-5
Methyl fluorosulfate
Magic methyl
Methyl fluorosulphate
Methyl fluosulfonate
methylfluorosulfonate
fluorosulfonyloxymethane
Fluorosulfuric acid, methyl ester
Methyl fluorosulphonate
Fluorosulfuric Acid Methyl Ester
CCRIS 1135
HSDB 4375
EINECS 207-004-3
Sulfuryl fluoride methyl ester
BRN 1098714
methyl fluoridosulfate
N015VFJ94Z
methyl sulfurofluoridate
DTXSID8073180
METHYL FLUOROSULFONATE [MI]
METHYL FLUOROSULFONATE [HSDB]
fluoridosulfuric acid (HSO_3_), methyl ester
UNII-N015VFJ94Z
SCHEMBL526480
DTXCID1040031
Fluorosulfonic Acid Methyl Ester
AKOS006221871
AS-80940
F0238
NS00031101
E78840
Q751430
Methyl Fluorosulfonate (stabilized with KF) [for Esterification]
207-004-3