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O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate

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Identification
Molecular formula
C6H12O2S3
CAS number
298-04-4
IUPAC name
O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate
State
State

The compound is in a liquid state at room temperature.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
236.70
Boiling point (Kelvin)
509.85
General information
Molecular weight
214.37g/mol
Molar mass
214.3650g/mol
Density
1.1250g/cm3
Appearence

The compound generally appears as a pale yellow liquid with a distinctive odor. It is typically clear, not cloudy, demonstrating homogeneity at room temperature.

Comment on solubility

Solubility of O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate

The compound O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate exhibits unique solubility characteristics that are crucial for its applications. Understanding its solubility behavior can be broken down into several key points:

  • Solvent Polarity: The solubility of this compound is significantly influenced by the polarity of the solvent. It tends to dissolve better in polar aprotic solvents compared to non-polar solvents.
  • Temperature Dependence: Like many organic compounds, its solubility is often temperature-dependent. Increased temperatures may enhance solubility due to higher kinetic energy and disruption of solvent-solute interactions.
  • Functional Groups: The presence of ethoxy and thioate groups contributes to its solubility traits. The thioate group is known for its ability to engage in hydrogen bonding, which can facilitate solubility in various environments.
  • Concentration Effects: At higher concentrations, this compound may reach a saturation point where solubility limits are observed, leading to potential precipitation.

In summary, the solubility of O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate is influenced by a combination of factors such as solvent properties, temperature, and structural components, making it an intriguing compound for further study. Always remember: solubility is not just a property; it's a gateway to functionality!

Interesting facts

Interesting Facts about O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate

O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate, a compound with a complex structure, belongs to a class of chemicals known for their unique properties and applications. Here are some intriguing aspects to consider:

  • Innovative Chemistry: The compound features a disulfide bond, which plays a vital role in the stability and reactivity of many biological molecules, particularly proteins and enzymes.
  • Pest Management: Due to its sulfur-containing functional groups, compounds like O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate may have potential applications in agriculture as pesticides or fungicides, helping manage agricultural pests and diseases.
  • Synthetic Versatility: The intricate structure suggests that this compound can be a valuable intermediate in organic synthesis, paving the way for the development of more complex molecules.
  • Research Importance: Understanding the properties and reactivity of thiol and thioether compounds can provide insights into biochemical processes and molecular interactions in living organisms.
  • Functional Group Dynamics: The presence of ethoxy and carbothioyl groups indicates interesting hydrogen bonding and electron-donating properties, which may influence the compound's reactions with various other chemical entities.

As a chemistry student or researcher, delving into the structural nuances of O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate can open pathways to fascinating discoveries in synthetic chemistry and material science. The interplay of its constituent functionalities showcases the beauty of chemical complexity!

Synonyms
Dixanthogen
502-55-6
Auligen
Diethyl dithiobis(thionoformate)
Aulinogen
Scabicidol
Bexide
Herbisan
Lenisarin
Silfasan
Xantoscabin
Diethyl dixanthogen
Galasan
Dixan
K Preparation
Bisethylxanthogen
BIS(ETHYLXANTHOGEN)
Skabilan
Diethyl xanthogenate
Diethylxanthogen disulfide
Diethyl dixanthogenate
Xanthogen, bis(ethyl-
Diethylxanthic disulfide
Dixanthogene
Dixantogeno
Bis(ethylxanthic)disulfide
Bisethylxanthogen disulfide
Ethylxanthogen disulfide
Antigal (VAN)
Diexanthogen
Dixanthogenum
Caswell No. 338
Diethyldithiobis thionoformate
DIETHYLDIXANTHOGEN
Herbisan 5
Diethyldithio bis(thionoformate)
Dixanthogen [INN:DCF]
Dixantogeno [INN-Latin]
Bis(ethylxanthic) disulfide
Dixanthogene [INN-French]
Dixanthogenum [INN-Latin]
O,O-Diethyl dithiobis(thioformate)
Ethylxanthic disulfide
Di-ethoxythiokarbonyl-disulfid
Dithiobis(thioformic acid) O,O-diethyl ester
Thioperoxydicarbonic acid diethyl ester
NSC 402561
Ethyl xanthogen disulfide
UNII-RN4CQ46FDM
RN4CQ46FDM
EINECS 207-944-4
Bis[ethylxanthogen]
Di-ethoxythiokarbonyl-disulfid [Czech]
Dixanthogen (INN)
EPA Pesticide Chemical Code 086501
NSC-402561
O,O-Diethyl ester of dithiobis(thioformic acid)
BRN 1781595
Formic acid, dithiobis(thio-, O,O-diethyl ester
BEXT (Salt/Mix)
DTXSID2041672
AI3-01649
O,O-Diethyl dithiobis[thioformate]
Thioperoxydicarbonic acid (((HO)C(S)S)2), diethyl ester
DIXANTHOGEN [MI]
DIXANTHOGEN [INN]
Thioperoxydicarbonic acid, diethyl ester
DIXANTHOGEN [WHO-DD]
Thioperoxydicarbonic acid ([(HO)C(S)]2S2), diethyl ester
DTXCID0021672
Diethyl dithiobis(thiono formate)
4-03-00-00416 (Beilstein Handbook Reference)
Thioperoxydicarbonic acid (((HO)C(S))2S2), diethyl ester
O,O-DIETHYL DITHIOBIS(THIONOFORMATE)
Thioperoxydicarbonic acid (((HO)C(S))2S2), OC,OC'-diethyl ester
Dixantogeno (INN-Latin)
Dixanthogene (INN-French)
Dixanthogenum (INN-Latin)
Formic acid, dithiobis[thio-, O,O-diethyl ester
ethoxy[(ethoxymethanethioyl)disulfanyl]methanethione
O,O-Diethyl ester of dithiobis[thioformic acid]
ethoxy((ethoxymethanethioyl)disulfanyl)methanethione
Thioperoxydicarbonic acid ([(HO)C(S)]2S2), OC,OC'-diethyl ester
O,O-diethyl dithiobisthioformate
P03AA01
207-944-4
fvigodvhavlzoo-uhfffaoysa-n
Aulin
Preparation K
EXD
CHEBI:82241
O-ethyl (ethoxycarbothioyldisulfanyl)methanethioate
NSC402561
NCGC00160587-01
Herbisan #5
[[ethoxy(sulfanylidene)methyl]disulfanyl]methanethioic acid O-ethyl ester
CAS-502-55-6
Bisethylxanthic disulfide
SCHEMBL37053
WLN: SUYO2&SSYUS&O2
CHEMBL331743
HY-B1186
o,o-diethyl dithiobis-(thioformate)
Tox21_111916
Tox21_302227
EX-A11901
AKOS024333295
CCG-213902
CS-4795
DB13712
NCGC00255506-01
MS-23434
DB-051741
NS00022244
C19120
D07366
F85253
1,1'-{Dithiobis[(thioxomethylene)oxy]}diethane
AB01563210_01
Q5284770
BRD-K05919151-001-01-6