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Thiosemicarbazone

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Identification
Molecular formula
C10H14BrN4OS
CAS number
79-19-6
IUPAC name
N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid
State
State

At room temperature, thiosemicarbazone is found in a solid state. Its structure prompts it to be stable under normal conditions, making it useful for storage and application in multiple chemical syntheses and industrial processes.

Melting point (Celsius)
173.00
Melting point (Kelvin)
446.00
Boiling point (Celsius)
195.00
Boiling point (Kelvin)
468.00
General information
Molecular weight
301.21g/mol
Molar mass
301.2110g/mol
Density
1.4200g/cm3
Appearence

Thiosemicarbazone typically appears as a crystalline solid, which may vary in color from white to pale yellow, depending on the exact molecular structure and purity. It is commonly found in a powder form for laboratory use.

Comment on solubility

Solubility of N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid

The solubility of N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid can be influenced by several factors, which make it an interesting compound to study:

  • Polarity: This compound contains various functional groups, including a thioic acid and an isothiazole moiety, which contribute to its overall polarity. The polarity affects how well the compound dissolves in different solvents.
  • Solvent Choice: It is likely to show varying degrees of solubility in polar solvents (e.g., water, alcohols) compared to non-polar solvents (e.g., hydrocarbons). Generally, polar compounds tend to dissolve better in polar solvents.
  • Temperature Effects: Increasing the temperature usually enhances the solubility of solids in liquids. Therefore, temperature adjustments might be beneficial when attempting to dissolve this compound.
  • pH Influence: Since this compound has a thioic acid group, the pH of the solution could significantly influence its solubility. At different pH levels, the ionization state of the thioic acid could change, which may enhance or decrease solubility.

In summary, while specific solubility data for N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid may not be abundantly available, factors such as polarity, solvent choice, temperature, and pH play crucial roles in determining its solubility characteristics. These considerations are essential for practical applications and further research in chemical sciences.

Interesting facts

Interesting Facts about N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid

N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid is a fascinating compound that exhibits unique characteristics and applications, primarily in the fields of chemistry and pharmacology. Below are some interesting insights about this chemical entity:

  • Structural Complexity: The compound features a distinctive structure that includes both isothiazole and morpholine rings, contributing to its biological activity and potential therapeutic uses.
  • Isothiazole Influence: The presence of the isothiazole moiety, especially with a bromo and methyl substitution pattern, plays a crucial role in enhancing the compound's reactivity and biological interactions.
  • Biological Activity: Compounds with similar structures have shown promising results as antimicrobial agents, signaling a potential for this compound in treating infectious diseases.
  • Research Interest: The integration of thioic acid functionality suggests potential applications in developing pharmaceuticals, including inhibitors for specific biochemical pathways.
  • Synthesis Applications: This compound serves as an excellent focal point in synthetic organic chemistry, highlighting the importance of multi-step synthesis techniques and the role of functional group transformations.

In summary, N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid is a noteworthy example of how structural diversity in chemical compounds can lead to novel applications in science. Its unique features inspire ongoing research and discovery.