Skip to main content

Thioacetamide

ADVERTISEMENT
Identification
Molecular formula
C4H6N4S2
CAS number
{null}
IUPAC name
2,3-bis[amino(methylsulfanyl)methylene]butanedinitrile
State
State

At room temperature, Thioacetamide is usually found in a solid state.

Melting point (Celsius)
108.00
Melting point (Kelvin)
381.00
Boiling point (Celsius)
221.00
Boiling point (Kelvin)
494.00
General information
Molecular weight
130.25g/mol
Molar mass
75.1330g/mol
Density
0.9800g/cm3
Appearence

Thioacetamide typically appears as a colorless or white crystalline solid.

Comment on solubility

Solubility of 2,3-bis[amino(methylsulfanyl)methylene]butanedinitrile (C4H6N4S2)

2,3-bis[amino(methylsulfanyl)methylene]butanedinitrile, a compound with a complex structure, exhibits particular solubility characteristics that are influenced by its functional groups and overall molecular structure. When considering the solubility of this compound, several important factors come into play:

  • Polarity: The presence of polar amino groups and methyl sulfide functionalities suggests that the compound may have a degree of solubility in polar solvents such as water or alcohols.
  • Hydrophobic Regions: Conversely, there may be hydrophobic characteristics due to the butanedinitrile portion, potentially limiting solubility in highly polar environments.
  • pH Sensitivity: The ionization of the amino groups might affect solubility in varying pH conditions, allowing for increased solubility in more acidic or basic solutions.
  • Temperature Dependence: Like many organic compounds, solubility may be affected by temperature, with increased solubility often observed at elevated temperatures.

In summary, the solubility of 2,3-bis[amino(methylsulfanyl)methylene]butanedinitrile can be predicted to be variable, depending on the solvent choice and environmental conditions. Understanding these solubility characteristics is crucial for applications in synthesis and formulation.

Interesting facts

Interesting Facts about 2,3-bis[amino(methylsulfanyl)methylene]butanedinitrile

2,3-bis[amino(methylsulfanyl)methylene]butanedinitrile is a fascinating compound that showcases the diversity and complexity of organic chemistry. Here are some interesting aspects:

  • Versatile Reactivity: This compound contains multiple functional groups, including amino and nitrile groups, which make it a subject of study for various chemical reactions such as substitution and addition reactions.
  • Biological Relevance: Compounds with similar structures are often explored for their biological activities, potentially acting as precursors for pharmaceuticals or agrochemicals.
  • Synthetic Pathways: The synthesis of 2,3-bis[amino(methylsulfanyl)methylene]butanedinitrile can involve a variety of synthetic methods, offering insights into multi-step organic synthesis techniques.
  • Research Potential: Due to its multi-functional nature, this compound has promising applications in material science and the development of novel catalysts.

Moreover, the presence of sulfur in the form of (methylsulfanyl) groups enhances the compound's properties, possibly affecting its reactivity and solubility characteristics. As noted by researchers, "the incorporation of sulfur atoms in organic molecules can lead to unique electronic and steric properties that are desirable in various applications." This characteristic makes it a valuable compound for ongoing research in both academic and industrial settings.

In summary, 2,3-bis[amino(methylsulfanyl)methylene]butanedinitrile is a remarkable example of the intricate designs found in organic compounds, embodying opportunities for exploration in chemistry's vast landscape.

Synonyms
108923-79-1
bis[amino(methylsulfanyl)methylidene]butanedinitrile
2,3-bis[amino(methylsulfanyl)methylidene]butanedinitrile
1,4-Diamino-2,3-dicyano-1,4-bis(methylthio)butadiene
HMS3268M04
DTXSID10274472