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(Diethylhydrazono)methanedithiol

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Identification
Molecular formula
C5H12N2S2
CAS number
7220-86-8
IUPAC name
(diethylhydrazono)methanedithiol
State
State

At room temperature, (Diethylhydrazono)methanedithiol is in a liquid state. It is a compound that can slowly oxidize in contact with air, thus requiring careful storage.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.15
General information
Molecular weight
180.30g/mol
Molar mass
180.3100g/mol
Density
1.0759g/cm3
Appearence

(Diethylhydrazono)methanedithiol typically appears as a yellow-orange oily liquid. It is often handled in a controlled environment due to its sensitivity to air and moisture.

Comment on solubility

Solubility of (diethylhydrazono)methanedithiol

The solubility of (diethylhydrazono)methanedithiol is an interesting topic due to the unique structure of this compound. Generally, compounds containing thiol groups, such as this one, can show varying solubility depending on several factors:

  • Polarity: The presence of the hydrazono functional group can influence the overall polarity of the molecule. Typically, polar compounds tend to be soluble in polar solvents, while non-polar compounds are more soluble in non-polar solvents.
  • Hydrogen Bonding: (diethylhydrazono)methanedithiol may engage in hydrogen bonding due to the presence of amine and thiol groups, which could enhance its solubility in water.
  • Chain Length: The diethyl groups add a hydrophobic character to the molecule, potentially reducing solubility in polar solvents.
  • Temperature: As with many substances, the solubility can change with temperature; increasing temperature often improves solubility for many compounds.

In summary, while (diethylhydrazono)methanedithiol could have some solubility in polar solvents due to its functional groups, the overall behavior will depend on the interplay of the aforementioned factors. As a rule of thumb, experimentation is necessary to determine the precise solubility characteristics of this compound. Understanding these dynamics can provide insights into its practical applications and behavior in various environments.

Interesting facts

Insights into (Diethylhydrazono)methanedithiol

(Diethylhydrazono)methanedithiol, also known for its intriguing molecular structure, presents a fascinating area of study in the field of chemistry. This compound features both hydrazone and dithiol functional groups, contributing to its unique reactivity and chemical behavior.

Key Characteristics

  • Hybrid Functional Group: The presence of hydrazone allows for potential tautomeric shifts, which could lead to significant variation in its properties.
  • Biological Activity: Compounds containing dithiol groups are often of interest in medicinal chemistry due to their potential anti-cancer properties.
  • Coordination Chemistry: The thiol groups in (diethylhydrazono)methanedithiol can form stable complexes with transition metals, making it a candidate for various catalysis applications.

Applications and Uses

The compound's chemical versatility opens the door to multiple applications:

  • Organic Synthesis: It can serve as an intermediate in the synthesis of more complex organic molecules.
  • Analytical Chemistry: Useful in the detection of metal ions through complex formation.
  • Research: Investigated for its behavior in various chemical environments, yielding insights into thiol and hydrazone interactions.

As the scientific community continues to explore (diethylhydrazono)methanedithiol, its potential in diverse applications highlights the importance of understanding the nuances of unique compounds. Not only does it reflect the complexity of chemical interactions, but it also emphasizes how such seemingly niche compounds can lead to significant breakthroughs in both theoretical and applied chemistry.