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5-Imino-1,2,4-dithiazole-3-thiol

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Identification
Molecular formula
C2H2N2S3
CAS number
61258-79-1
IUPAC name
5-imino-1,2,4-dithiazole-3-thiol
State
State

At room temperature, 5-Imino-1,2,4-dithiazole-3-thiol typically exists in a solid state. It may be slightly soluble in some organic solvents.

Melting point (Celsius)
140.00
Melting point (Kelvin)
413.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
164.24g/mol
Molar mass
164.2430g/mol
Density
1.5932g/cm3
Appearence

The compound typically appears as a solid powder with a yellow to brown color, reflecting its sulfur content.

Comment on solubility

Solubility of 5-imino-1,2,4-dithiazole-3-thiol

The solubility characteristics of 5-imino-1,2,4-dithiazole-3-thiol are intriguing due to its unique structure and functional groups, which can significantly affect its solvation behavior. Here are some critical points to consider:

  • Polarity: The presence of thiol (-SH) and imino (=NH) groups typically increases the compound's polarity, enhancing its ability to interact with polar solvents such as water.
  • Hydrogen Bonding: The capability of 5-imino-1,2,4-dithiazole-3-thiol to form hydrogen bonds can facilitate its solubility in polar environments, making it more soluble in solvents like alcohols.
  • Influence of pH: The solubility of this compound may be pH-dependent, with different solubility profiles in acidic or basic media due to protonation or deprotonation of functional groups.
  • Solvent Interactions: It may exhibit variable solubility in organic solvents based on the solvent's ability to interact with the compound's functional groups.

In summary, while the solubility of 5-imino-1,2,4-dithiazole-3-thiol in water could be expected to be reasonable due to its polar moieties, laboratory experimentation is essential to determine its precise solubility parameters. Understanding these factors can provide valuable insights into its practical applications and behavior in various chemical contexts.

Interesting facts

Interesting Facts about 5-Imino-1,2,4-dithiazole-3-thiol

5-Imino-1,2,4-dithiazole-3-thiol is a fascinating compound that brings both intrigue and utility in the field of chemistry. Here are some noteworthy aspects of this compound:

  • Structural Diversity: This compound features a unique ring structure composed of nitrogen and sulfur atoms, showcasing the diversity of heterocyclic compounds. The presence of both an imino group and a thiol moiety enhances its reactivity and potential applications.
  • Potential Applications: Compounds like 5-imino-1,2,4-dithiazole-3-thiol are often studied for their potential use in leading-edge technologies, such as photovoltaics and semiconductor materials. Their distinct electronic properties make them candidates for innovative materials.
  • Bioactivity: Research suggests that heterocycles similar to this compound may exhibit biological activities, such as antimicrobial or antitumor effects, making them of interest in medicinal chemistry. Scientists are continually exploring their biochemical pathways and therapeutic potentials.
  • Research and Development: The synthesis of 5-imino-1,2,4-dithiazole-3-thiol can be a subject of innovative research, particularly in the realm of developing new synthetic methodologies or optimizing conditions to enhance yield and purity.
  • Exploration of Reactivity: The reactive thiol group provides insight into nucleophilic substitution and addition reactions, which can be critical for synthesizing more complex organic molecules. Understanding these pathways can open doors to new chemical explorations.

In summary, 5-imino-1,2,4-dithiazole-3-thiol is more than just a compound; it represents an intersection of various fields within chemistry that could lead to significant advancements. As science progresses, keeping an eye on such compounds can lead to unexpected discoveries and breakthroughs.