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Thioacetohydrazide

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Identification
Molecular formula
C2H5N3S2
CAS number
16845-22-4
IUPAC name
1-[amino(sulfanyl)methylene]isothiourea
State
State

At room temperature, Thioacetohydrazide is typically found in a solid state. It is stable under normal conditions, but needs to be stored properly to maintain its integrity.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
173.00
Boiling point (Kelvin)
446.15
General information
Molecular weight
105.16g/mol
Molar mass
105.1570g/mol
Density
1.5200g/cm3
Appearence

Thioacetohydrazide appears as a white crystalline solid. It may also occur as a powder form, depending on its preparation and purity.

Comment on solubility

Solubility of 1-[amino(sulfanyl)methylene]isothiourea

1-[amino(sulfanyl)methylene]isothiourea exhibits unique solubility characteristics that are influenced by its chemical structure. The presence of amino and thiol functional groups plays a significant role in its interaction with solvents.

Key points regarding its solubility:

  • Polar Character: The compound is polar due to the amino group (-NH2) and thiol group (-SH), which can engage in hydrogen bonding with water.
  • Solvent Compatibility: It is likely to be more soluble in polar solvents such as water or methanol, while showing limited solubility in non-polar solvents like hexane.
  • pH Dependence: The solubility may vary with pH; at different pH levels, the ionization state of the amino group can affect the overall solubility.

In summary, when assessing the solubility of 1-[amino(sulfanyl)methylene]isothiourea, it is essential to consider these factors to predict its behavior in various chemical environments. The interplay of polar functional groups and solvent properties will continue to be an area of interest for researchers exploring its applications.

Interesting facts

Interesting Facts about 1-[amino(sulfanyl)methylene]isothiourea

1-[amino(sulfanyl)methylene]isothiourea is a fascinating compound that combines elements of both organosulfur chemistry and organic synthesis. This compound is known for its unique structural features and potential applications in various fields. Here are some interesting points about this intriguing chemical:

  • Dual Functional Group: The presence of both amino and sulfanyl functional groups allows the compound to participate in a variety of chemical reactions, enhancing its utility in synthetic organic chemistry.
  • Biological Significance: Isothioureas are often studied for their biological properties. They can act as precursors to bioactive compounds and are of interest in medicinal chemistry.
  • Research Applications: This compound is a subject of ongoing research, particularly in the fields of pharmaceuticals. Its derivatives are explored for potential therapeutic uses, including anticancer and antimicrobial agents.
  • Structural Diversity: The isothiourea scaffold can be modified in various ways leading to a range of derivatives, each with unique physical and chemical properties.

As chemists continue to explore the potential of 1-[amino(sulfanyl)methylene]isothiourea, it showcases the complex interplay between molecular structure and biological activity, emphasizing the **importance of synthetic chemistry** in developing new compounds with potential therapeutic benefits. Each discovery in this realm contributes to our understanding of how molecular modifications can lead to significant innovation in **drug design** and **development**.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." 1-[amino(sulfanyl)methylene]isothiourea is a prime example of how exploring chemical structures can lead to innovative ideas and applications in **science and technology**.