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O-butyl S-(2-butoxycarbonothioylsulfanyl)ethanethioate

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Identification
Molecular formula
C11H20O3S3
CAS number
1068796-77-5
IUPAC name
O-butyl 2-butoxycarbothioylsulfanylethylsulfanylmethanethioate
State
State

This compound is a liquid at room temperature. It is relatively stable, though it should be handled with care to prevent exposure to its vapors, which could be an irritant.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
276.44g/mol
Molar mass
276.4440g/mol
Density
1.0563g/cm3
Appearence

This compound appears as a liquid, typically with a pale yellow color. It is non-volatile and has a distinct odor characteristic of thioesters, which can be described as sulfurous and fruity.

Comment on solubility

Solubility of O-butyl 2-butoxycarbothioylsulfanylethylsulfanylmethanethioate

The solubility of O-butyl 2-butoxycarbothioylsulfanylethylsulfanylmethanethioate in various solvents can be quite intriguing. Understanding this compound's solubility involves several key factors:

  • Polarity: The presence of both hydrophobic and hydrophilic components suggests that the solubility may differ significantly in polar versus non-polar solvents.
  • Chain Length: The butyl group contributes to hydrophobic characteristics, which may limit solubility in water while enhancing solubility in organic solvents.
  • Functional Groups: The functional groups, particularly the thioate, might interact favorably with certain solvents, enhancing solubility.

As an interesting note, compounds with similar structures often exhibit solubility behaviors characterized by:

  • Higher solubility in organic solvents such as acetone, ethanol, and ether.
  • Lower solubility in water, given the increased hydrophobic characteristics due to longer hydrocarbon chains.
  • Temperature dependence, where increased temperatures can improve solubility in solvents by lowering viscosity and increasing molecular interactions.

In summary, while it is not straightforward to pin down specific solubility values without empirical data, the interplay of polarity, functional groups, and solvent characteristics will significantly influence the solubility profile of O-butyl 2-butoxycarbothioylsulfanylethylsulfanylmethanethioate. Further studies could provide precise solubility information, enriching our understanding of this intriguing compound.

Interesting facts

Interesting Facts about O-butyl 2-butoxycarbothioylsulfanylethylsulfanylmethanethioate

O-butyl 2-butoxycarbothioylsulfanylethylsulfanylmethanethioate is a complex compound that exhibits fascinating characteristics and properties that could intrigue both chemists and students alike. Here are some interesting points to consider:

  • Versatile Functional Groups: This compound features a variety of functional groups, including thioate and butoxy groups, which play significant roles in its reactivity and interactions with other molecules.
  • Potential Applications: Compounds like O-butyl 2-butoxycarbothioylsulfanylethylsulfanylmethanethioate may find applications in agrochemicals, where their efficacy as pesticides or herbicides could be explored.
  • Mechanism of Action: The unique structure allows it to participate in various chemical reactions that can help in understanding sulfur chemistry and its role in organic synthesis.
  • Research Significance: The intricate nature of this compound makes it a potential candidate for studies aimed at discovering new materials with specific properties, which could lead to breakthroughs in diverse fields like material science or medicinal chemistry.
  • Educational Value: For students learning about organic compounds, this molecule serves as an excellent example of how complex structures can be synthesized and how different groups influence overall reactivity and polarity.

In conclusion, O-butyl 2-butoxycarbothioylsulfanylethylsulfanylmethanethioate is more than just a name; it represents a story of molecular complexity and a gateway to understanding the principles of chemistry in real-world applications. As said by renowned chemist Linus Pauling, “The science of chemistry is the science of change,” and compounds like these are perfect illustrations of that dynamic nature.

Synonyms
Ethylene bis(butylxanthate)
LZ 6/9T
Xanthic acid, butyl-, ethylene ester
P4J5WG8RD5
NSC 220090
BRN 1795954
Xantic acid, ethylenebis-, O-butyl ester
UNII-P4J5WG8RD5
NSC-220090
CARBONIC ACID, ETHYLENEBIS(DITHIO-, O,O'-DIBUTYL ESTER
Carbonodithioic acid, S,S'-1,2-ethanediyl O,O'-dibutyl ester
DTXSID50184768
4-03-00-00412 (Beilstein Handbook Reference)
ETHYLENE BIS(BUTYL XANTHATE)
DTXCID90107259
Carbonodithioic acid, S,S'-1,2-ethanediyl O,O'-dibutyl ester (9CI)
3074-80-4
Xantic acid, o-butyl ester
WLN: SUYO4&S2SYUS&O4
Carbonic acid, O,O'-dibutyl ester
NSC220090
Carbonodithioic acid,S'-1,2-ethanediyl O,O'-dibutyl ester