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Ethoxymethanedithioic acid

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Identification
Molecular formula
C3H6OS2
CAS number
38156-58-8
IUPAC name
ethoxymethanedithioic acid
State
State
The compound is usually in a liquid state at room temperature.
Melting point (Celsius)
-99.50
Melting point (Kelvin)
173.70
Boiling point (Celsius)
196.50
Boiling point (Kelvin)
469.60
General information
Molecular weight
122.19g/mol
Molar mass
122.1930g/mol
Density
1.2098g/cm3
Appearence

Ethoxymethanedithioic acid is typically presented as a colorless to pale yellow liquid. It is sometimes referred to in the form of an ester or a salt, primarily used in organic synthesis.

Comment on solubility

Solubility of Ethoxymethanedithioic Acid

Ethoxymethanedithioic acid, with the chemical formula C4H8O2S2, exhibits specific solubility characteristics that are intriguing to explore. Generally, the solubility of a compound can be significantly influenced by its molecular structure, polarity, and the presence of functional groups.

Key Points About Solubility

  • Ethoxymethanedithioic acid contains both an ether functional group (due to the ethoxy part) and a dithioacid component, contributing to its solubility profile.
  • The polar nature of the ether group often enhances solubility in polar solvents, making it more soluble in water compared to non-polar solvents.
  • Its dithioic acid component can participate in hydrogen bonding, which may improve solubility in certain aqueous environments.

In summary, while further empirical data would provide precise solubility values, the presence of both polar and non-polar elements in ethoxymethanedithioic acid suggests that it is likely soluble in polar solvents and may exhibit limited solubility in non-polar solvents. This dual character can lead to interesting applications in various chemical processes.

Interesting facts

Interesting Facts about Ethoxymethanedithioic Acid

Ethoxymethanedithioic acid, known for its unique chemical structure, is a compound that offers intriguing possibilities in both organic synthesis and environmental chemistry. Its dithioic acid moiety enhances its potential in a variety of chemical reactions.

Key Properties and Applications

  • Synthetic Utility: Ethoxymethanedithioic acid is valuable in the synthesis of other chemical compounds. It can serve as a building block in organic chemistry, particularly in the formation of complex molecules.
  • Reactivity: The presence of sulfur atoms contributes to its reactivity, allowing for unique pathways in chemical transformations, such as nucleophilic substitutions.
  • Biochemical Relevance: The compound may have implications in biochemical research, particularly in the study of thiol-based reactions and their roles in biological systems.
  • Environmental Chemistry: Its derivatives could potentially be explored for their ability to interact with heavy metals, suggesting its role in pollution mitigation strategies.

As scientists continue to explore the potential of ethoxymethanedithioic acid, they often quote the importance of understanding the properties of sulfur-containing compounds: "In the world of chemistry, sulfur is often the unsung hero, involved in reactions that define life itself."

Research Opportunities

There is a growing interest in the exploration of this compound for novel applications, including:

  • Investigation into its role as a catalyst in chemical reactions.
  • Studying its potential pharmacological activities.
  • Exploring its interactions with various environmental pollutants.

With its fascinating characteristics and potential applications, ethoxymethanedithioic acid continues to be a subject of research and discussion in the chemical community, highlighting the importance of sulfur-containing compounds in advancing our understanding of both theoretical and applied chemistry.

Synonyms
ETHYLXANTHATE
Ethyl xanthogenate
Ethyl xanthate
Xanthogenic acid
Ethylxanthic acid
151-01-9
Xanthate
O-Ethyl hydrogen dithiocarbonate
ethoxymethanedithioic acid
Ethylxanthogenic acid
Xanthic acid, ethyl-
Ethoxydithioformic acid
O-Ethyl dithiocarbamate
O-Ethyl dithiocarbonate
Xanthogenic acid, ethyl-
Carbonodithioic acid, O-ethyl ester
Carbonic acid, dithio-, O-ethyl ester
HSDB 5652
EINECS 205-780-8
BRN 1740597
B7B55M6MK1
ETHYLXANTHATE [HSDB]
4-03-00-00401 (Beilstein Handbook Reference)
UNII-B7B55M6MK1
Xanthogensaure
ethyl xanthic acid
cobalt ethylxanthate
O-ethylxanthic acid
Xanthic acid, ethyl
OEthyl dithiocarbonate
Xanthogenic acid, ethyl
O-ethyldithiocarbonic acid
SCHEMBL5690
OEthyl hydrogen dithiocarbonate
CHEMBL3039661
DTXSID3045063
dithiocarbonic acid o-ethyl ester
O-Ethyl hydrogen carbonodithioate
ZOOODBUHSVUZEM-UHFFFAOYSA-N
Carbonodithioic acid, Oethyl ester
Carbonic acid, dithio, Oethyl ester
DB-255876
NS00008455
Q27274459
205-780-8