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Chloromethyl methyl sulfide

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Identification
Molecular formula
C2H5ClS
CAS number
2759-07-7
IUPAC name
chloro(methylsulfanyl)methane
State
State

Chloromethyl methyl sulfide is in a liquid state at room temperature.

Melting point (Celsius)
-90.00
Melting point (Kelvin)
183.15
Boiling point (Celsius)
126.00
Boiling point (Kelvin)
399.15
General information
Molecular weight
96.57g/mol
Molar mass
96.5700g/mol
Density
1.1810g/cm3
Appearence

Chloromethyl methyl sulfide is a colorless to pale yellow liquid. It can have a slightly unpleasant odor reminiscent of cabbage or garlic due to the presence of the sulfur-containing group.

Comment on solubility

Solubility of Chloro(methylsulfanyl)methane

Chloro(methylsulfanyl)methane, also known by its chemical formula C2H6ClS, exhibits unique solubility properties that are of interest in various chemical applications.

In terms of its solubility profile:

  • Polar Solvents: Chloro(methylsulfanyl)methane tends to be more soluble in polar solvents due to the electronegative chlorine atom and the sulfur moiety, which can engage in dipole-dipole interactions.
  • Non-Polar Solvents: Its solubility diminishes in non-polar solvents because of the compound's polar characteristics. Hence, non-polar interactions are less favorable.
  • Water Solubility: The compound has limited solubility in water, which can be attributed to its hydrophobic alkyl group and the presence of the chloromethyl group that disrupts hydrogen bonding with water molecules.

It is crucial to emphasize that the overall solubility of chloro(methylsulfanyl)methane is influenced by temperature, concentration, and the presence of other solutes in the solvent system. As a result, you may often encounter varying solubility behavior under different conditions.

To summarize, "the solubility of chloro(methylsulfanyl)methane is a fascinating area of study that highlights the intricate relationship between molecular structure and solvent interactions." Understanding these principles is essential for its effective utilization in chemical research and applications.

Interesting facts

Interesting Facts about Chloro(methylsulfanyl)methane

Chloro(methylsulfanyl)methane, commonly known in the field of organic chemistry, is an intriguing compound with unique properties and applications. Here are some captivating aspects of this compound:

  • Structure and Bonding: This compound features both a chloromethyl and a methylsulfanyl group, presenting a fascinating example of how different functional groups can interact. The presence of sulfur in its structure gives it distinct chemical behavior compared to similar alkyl halides.
  • Reactivity: The chloromethyl functional group is known for its reactivity in nucleophilic substitution reactions, making chloro(methylsulfanyl)methane a valuable intermediate in synthesizing more complex organic molecules. Its reactivity can be harnessed to create various derivatives.
  • Applications: This compound finds its place in pharmaceuticals and agrochemicals, where it may act as a precursor for the synthesis of active compounds. It serves as a testament to how simple chemical transformations can lead to significant advancements in medicine and agriculture.
  • Toxicity and Safety: As with many chlorinated compounds, safety is paramount. Proper handling is crucial because exposure can lead to health risks. Understanding its toxicity profile is important for researchers working with it in the laboratory.
  • Environmental Concerns: The environmental impact of chlorinated compounds, including chloro(methylsulfanyl)methane, raises awareness about the importance of sustainable practices in chemical manufacturing and usage, pushing for greener alternatives whenever possible.

In summary, chloro(methylsulfanyl)methane is more than just a name in the world of chemistry; it represents a class of compounds that illustrates the delicate interplay between molecular structure, reactivity, and practical application. Exploring its properties not only enhances our understanding of organic chemistry but also emphasizes the significance of responsible chemical practices.

Synonyms
Chloromethyl methyl sulfide
2373-51-5
Chlorodimethyl sulfide
CH3SCH2Cl
CCRIS 7530
Chloromethylmethyl sulfide
EINECS 219-148-4
.alpha.-Chlorodimethyl sulfide
BRN 1730851
AI3-61511
DTXSID10178406
4-01-00-03079 (Beilstein Handbook Reference)
alpha-Chlorodimethyl sulfide
DTXCID00100897
inchi=1/c2h5cls/c1-4-2-3/h2h2,1h
jwmlccrpdoibav-uhfffaoysa-n
Chloro(methylsulfanyl)methane
Methane, chloro(methylthio)-
Chloromethyl methyl thioether
Methylthiomethyl chloride
Chloro(methylthio)methane
Chloromethyl methyl sulphide
Chlorodimethyl thioether
Monochlorodimethyl sulfide
chloromethylmethylsulfide
Clorodimetilsolfuro
SULFIDE, CHLOROMETHYL METHYL
NSC 63205
Clorodimetilsolfuro [Italian]
MFCD00000923
methylthiomethylchloride
chloromethylmethylsulfane
chloromethyl methylsulfide
chloromethylmethylthioether
chloromethylsulfanylmethane
chloro-(methylthio)methane
(chloromethyl)methylsulfide
chloromethyl methylthioether
chloro-methylsulfanyl-methane
(chloromethyl)(methyl)sulfane
(Chloromethyl) methyl sulfide
chloranyl(methylsulfanyl)methane
Chloro(methylsulfanyl)methane #
Chloromethyl methyl sulfide, 95%
Methane,chloro(methylthio)-(9ci)
NSC63205
STR09358
NSC-63205
AKOS006223733
NS00027475
EN300-79429
F20413
A816870
Chloromethyl methyl sulfide, stabilized over potassium carbonate