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O-(2-Methylcyclohexyl) methylsulfanylmethanethioate

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Identification
Molecular formula
C11H20OS2
CAS number
.
IUPAC name
O-(2-methylcyclohexyl) methylsulfanylmethanethioate
State
State

At room temperature, the compound commonly exists in a liquid state.

Melting point (Celsius)
-8.00
Melting point (Kelvin)
265.15
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.15
General information
Molecular weight
192.34g/mol
Molar mass
192.3400g/mol
Density
1.0654g/cm3
Appearence

The compound is typically a colorless or pale yellow liquid. It might have a distinct thioester odor due to the presence of sulfur groups.

Comment on solubility

Solubility of O-(2-methylcyclohexyl) methylsulfanylmethanethioate

O-(2-methylcyclohexyl) methylsulfanylmethanethioate exhibits intriguing solubility characteristics, primarily influenced by its molecular structure and functional groups. Here are some key points regarding its solubility:

  • Polar vs. Nonpolar: The presence of the methylsulfanyl group contributes to a balance of polar and nonpolar characteristics, suggesting that this compound might be more soluble in organic solvents than in water.
  • Solvent Compatibility: It is likely to dissolve well in solvents such as ethanol, methanol, and acetone due to their polar nature.
  • Hydrophobic Regions: The cyclohexyl group creates hydrophobic regions, which can hinder solubility in polar media like water.
  • Temperature Influence: Temperature can play a crucial role in enhancing solubility; typically, an increase in temperature may lead to an increase in solubility for many organic compounds.

In summary, while the precise solubility data for O-(2-methylcyclohexyl) methylsulfanylmethanethioate may require empirical validation, it's reasonable to conclude that it is more soluble in organic solvents than in aqueous solutions due to its structural features. As a general rule, remember: “Like dissolves like.” This principle is fundamental when predicting the solubility of compounds based on their functional groups and structure.

Interesting facts

Interesting Facts About O-(2-Methylcyclohexyl) Methylsulfanylmethanethioate

O-(2-Methylcyclohexyl) methylsulfanylmethanethioate is a fascinating compound that showcases the intriguing nature of organosulfur chemistry. Here are some interesting aspects to consider:

  • Unique Structure: The compound contains a methylsulfanylmethanethioate group, which is characterized by the presence of sulfur, making it an important example of thioester functionalities in organic chemistry.
  • Biological Relevance: Compounds like this often have applications in biological systems. For example, thioesters are commonly involved in enzyme mechanisms and metabolic pathways.
  • Odor and Flavor: Many sulfur-containing compounds are known for their distinctive odors. This raises questions about the pleasant or unpleasant scents associated with different organosulfur compounds and their potential uses in flavoring.
  • Industrial Applications: The chemistry of sulfides and thiols often leads to their use in agrochemicals, pharmaceuticals, and as intermediates in chemical synthesis, making them valuable in industrial processes.
  • Solvent Properties: The presence of the cyclohexyl ring can influence the solvation properties of this compound, affecting its reactivity and interaction with other substances.

As a scientist or a student, exploring compounds like O-(2-methylcyclohexyl) methylsulfanylmethanethioate not only enhances your understanding of functional groups and their properties but also opens up pathways to innovative applications in various fields.

In the words of renowned chemist Linus Pauling, "The best way to understand the chemistry of a substance is to study its structure and properties." This compound is a perfect illustration of that principle.

Synonyms
15288-12-7
S-METHYL O-(2-METHYLCYCLOHEXYL) DITHIOCARBONATE
DTXSID90934623
S-methyl O-(2-methylcyclohexyl) carbonodithioate