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Cyclohexyl 2-mercaptoacetate

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Identification
Molecular formula
C8H14O2S
CAS number
881-94-7
IUPAC name
cyclohexyl 2-sulfanylacetate
State
State

At room temperature, cyclohexyl 2-mercaptoacetate is in a liquid state.

Melting point (Celsius)
-25.10
Melting point (Kelvin)
248.05
Boiling point (Celsius)
274.60
Boiling point (Kelvin)
547.75
General information
Molecular weight
190.29g/mol
Molar mass
190.2860g/mol
Density
1.1330g/cm3
Appearence

Cyclohexyl 2-mercaptoacetate appears as a clear to pale yellow liquid. It generally has a characteristic sulfurous odor, which is typical for thiol-containing compounds.

Comment on solubility

Solubility of Cyclohexyl 2-sulfanylacetate

Cyclohexyl 2-sulfanylacetate, known for its unique structure, presents specific solubility characteristics that can influence its applications in various fields. Its solubility in different solvents is governed primarily by its molecular interactions.

Key Solubility Properties:

  • Polar Solvents: Cyclohexyl 2-sulfanylacetate is typically more soluble in polar solvents such as water and alcohols due to hydrogen bonding and dipole-dipole interactions.
  • Non-Polar Solvents: Conversely, it is less soluble in non-polar solvents like hexane, which do not favor interactions with this polar compound.
  • Temperature Dependence: The solubility may also vary with temperature; generally, an increase in temperature can lead to enhanced solubility.

In summary, the solubility of cyclohexyl 2-sulfanylacetate can be described as:

  1. Highly soluble in polar solvents.
  2. Less soluble in non-polar solvents.
  3. Dependent on temperature.

Understanding these solubility traits is crucial for researchers and industries aiming to utilize cyclohexyl 2-sulfanylacetate effectively in chemical processes or formulations.

Interesting facts

Interesting Facts about Cyclohexyl 2-Sulfanylacetate

Cyclohexyl 2-sulfanylacetate is a fascinating chemical compound notable for its unique structure and diverse applications. Here are some captivating insights:

  • Functional Group Significance: The compound features a sulfanyl group (-SH), which imparts distinct properties and reactivity. This group can participate in a variety of chemical reactions, including nucleophilic substitutions, making the compound significant in synthetic chemistry.
  • Applications in Organic Synthesis: Cyclohexyl 2-sulfanylacetate is often employed in the synthesis of more complex organic molecules. Specifically, it's used to introduce sulfur into organic frameworks, providing a pathway to develop pharmaceuticals and agrochemicals.
  • Odor and Flavor Components: Compounds like cyclohexyl 2-sulfanylacetate can be integral in flavor and fragrance chemistry. The presence of the cyclohexyl group contributes to their aromatic profile, making them desirable in creating specific scents and tastes.
  • Chirality: Depending on the synthesis route, the compound can exhibit chirality, leading to enantiomers that may have differing biological activities. Studying these differences can reveal important insights for medicinal chemistry and pharmacology.
  • Research Potential: As scientists explore the vast chemical landscape, cyclohexyl 2-sulfanylacetate is a subject of ongoing research for its potential uses in various fields such as materials science and drug development.

In conclusion, cyclohexyl 2-sulfanylacetate exemplifies the intricate nature of organic chemistry, showcasing how even a seemingly simple compound can play a significant role in advances across multiple scientific domains. As the quote goes, "Chemistry is the art of understanding the molecules that define our world." With compounds like this, we continue to unlock new possibilities.

Synonyms
16849-98-2
Cyclohexyl mercaptoacetate
Cyclohexyl thioglycolate
Cyclohexyl 2-mercaptoacetate
Acetic acid, mercapto-, cyclohexyl ester
EINECS 240-874-2
DTXSID00168573
DTXCID5091064
240-874-2
DHQYDHVETSVMKQ-UHFFFAOYSA-N
cyclohexyl 2-sulfanylacetate
Acetic acid, 2-mercapto-, cyclohexyl ester
cyclohexyl2-sulfanylacetate
Cyclohexyl sulfanylacetate #
V2Y33HW2FV
SCHEMBL1405464
SCHEMBL4678698
RAA84998
AKOS006271792
CS-0237760
NS00025531
EN300-186774
G22818