Skip to main content

O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate

ADVERTISEMENT
Identification
Molecular formula
C6H12O2S4
CAS number
50782-69-9
IUPAC name
O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate
State
State

The compound is in a liquid state at room temperature, characterized by its distinct sulfur-like odor and yellow color.

Melting point (Celsius)
-35.00
Melting point (Kelvin)
238.15
Boiling point (Celsius)
381.85
Boiling point (Kelvin)
655.00
General information
Molecular weight
274.47g/mol
Molar mass
274.4700g/mol
Density
1.2400g/cm3
Appearence

The compound is generally a pale yellow liquid at room temperature. It is also known to have a slightly unpleasant odor, typical of some organosulfur compounds. It may change its appearance slightly due to impurities or exposure.

Comment on solubility

Solubility of O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate

Understanding the solubility of O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate can provide valuable insights into its potential applications and behavior in various environments. Here are some observations regarding its solubility:

  • Polar vs Non-Polar Solvents: The solubility of this compound is primarily influenced by its molecular structure. Compounds with significant polar functional groups typically exhibit better solubility in polar solvents like water, while non-polar solvents (e.g., hexane) promote solubility in non-polar substances.
  • Hydrophobic Effects: With the presence of sulfanyl groups, which are generally hydrophobic, this compound might show limited solubility in water while being more soluble in organic solvents.
  • Temperature Dependency: Solubility can also vary with temperature, where higher temperatures may increase the solubility of certain compounds in solvents due to enhanced molecular interactions.

To summarize, the solubility of O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate is likely contingent upon the solvent system employed and the specific conditions, making it essential to consider these factors during experimental applications.

Interesting facts

Interesting Facts About O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate

O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate is a fascinating compound with several intriguing aspects that make it a subject of interest for chemists and researchers alike. Here are some key points:

  • Combining Elements: This compound features a unique combination of sulfur and carbon atoms, demonstrating the versatile chemistry of sulfur, particularly in the formation of thioate (sulfur-containing) esters.
  • Pesticide Potential: Compounds with similar functional groups to O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate have been explored for their potential use as agrochemicals. They may serve as effective pesticide agents, showcasing the ongoing search for safer alternatives in agriculture.
  • Synthesis Routes: The synthesis of this compound involves complex synthetic pathways that can yield intriguing results, making it an interesting target for organic chemists. Such synthesis often includes the manipulation of precursor compounds and the careful handling of sulfur species.
  • Reactivity: The presence of multiple functional groups in the molecule may lead to interesting reactivity patterns, especially in nucleophilic substitutions and other organic reactions, proving its utility in synthetic organic chemistry.
  • Potential Applications: Beyond pesticides, compounds like this are also studied for their roles in pharmaceuticals and as biochemical probes, which may affect a variety of biological systems due to their ability to interact with proteins and enzymes.

In summary, O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate exemplifies the rich and multifaceted world of chemistry, where the interplay of elements can lead to significant scientific developments and practical applications. As research progresses, who knows what additional secrets this compound might reveal!

Synonyms
Defoliant 713
Bisethylxanthate trisulfide
Di(ethylxanthogen) trisulfide
Bis(ethylxanthogen)trisulfide
Bis(ethylxanthogen) trisulfide
Trisulfide, bis(ethoxythioxomethyl)
Bis(ethoxythiocarbonyl)trisulfide
Di(ethylxanthogen)trisulfide
W7PX1UP1IS
Methanethioic acid, trithiobis-, O,O-diethyl ester
Trisulfide, bis(ethoxythiocarbonyl)-
FORMIC ACID, TRITHIOBIS(THIO-, O,O-DIETHYL ESTER
Di-ethoxythiokarbonyl-trisulfid
NSC 402562
Di-ethoxythiokarbonyl-trisulfid [Czech]
BRN 1788565
UNII-W7PX1UP1IS
NSC-402562
DTXSID70171716
3-03-00-00351 (Beilstein Handbook Reference)
DTXCID8094207
Methanethioic acid, trithiobis-, O,O-diethyl ester (9CI)
BEXT
1851-77-0
O-ethyl (ethoxycarbothioyltrisulfanyl)methanethioate
Bis-ethylxanthogen trisulfide
Trisulfide, bis(ethoxythiocarbonyl)
NSC402562
Pertrithiobis(thioformic acid O-ethyl) ester
BEXT (VAN)
WLN: SUYO2&SSSYUS&O2
CHEMBL1998620
1,3-Bis(ethoxycarbothioyl)trisulfane
NCI60_003780
Formic acid, {trithiobis[thio-,} O,O-diethyl ester