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Methylisothiazolinone iodide

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Identification
Molecular formula
C7H9BrIN4S2
CAS number
null
IUPAC name
3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea;iodide
State
State

At room temperature, this compound is found in a solid state. Its crystalline nature makes it relatively stable under ambient conditions, provided it is stored away from potential reactants like water or oxidizing agents.

Melting point (Celsius)
218.00
Melting point (Kelvin)
491.15
Boiling point (Celsius)
316.00
Boiling point (Kelvin)
589.15
General information
Molecular weight
291.10g/mol
Molar mass
291.0980g/mol
Density
2.7803g/cm3
Appearence

This compound typically appears as a crystalline solid, often bearing a yellow to orange-brown color. The presence of iodine often contributes to the intense coloration. It's important to handle this material under controlled conditions to prevent contact with moisture and light, which can cause degradation or photochemical reactions.

Comment on solubility

Solubility of 3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea;iodide

The solubility of 3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea;iodide can be influenced by various factors due to its complex structure. Here are several key points to consider:

  • Polarity: The presence of iodide ions may enhance solubility in polar solvents, making it more soluble in aqueous environments.
  • Functional Groups: The isothiazole and isothiourea moieties can affect the solubility profile. Compounds containing nitrogen and sulfur often exhibit higher solubility in polar solvents.
  • Hydrophobic Interactions: The bromo and methyl groups may introduce some hydrophobic character, potentially reducing solubility in purely aqueous conditions.
  • Temperature Effects: Like many organic compounds, solubility can increase with an increase in temperature, thus affecting the practical applications in solution.

Overall, the solubility of this compound can be summarized as being potentially higher in polar solvents, moderated by its hydrophobic groups. As with many chemical compounds, it may require systematic examination to identify the optimal solvent conditions for its solubility and stability.

Interesting facts

Interesting Facts about 3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea;iodide

This fascinating compound is a member of the isothiourea family, which are known for their diverse biological activities. Here are some intriguing aspects of this compound:

  • Biological Significance: Compounds containing isothiourea groups are often investigated for their pharmacological potential, exhibiting properties such as antiviral, antibacterial, and antiproliferative effects.
  • Unique Structure: The bromine substitution on the isothiazole ring enhances the compound's reactivity and can contribute to its biological activity.
  • Applications: Due to its unique structure, this compound has potential applications in drug design, particularly in the development of new therapies for diseases.
  • Research Interest: Scientists are increasingly interested in isothiourea derivatives for their ability to inhibit enzymes and serve as bioactive compounds in medicinal chemistry.
  • Mechanistic Studies: Understanding how this compound interacts at the molecular level can provide insights into novel therapeutic strategies.

As noted by chemists in their research, "The exploration of isothiourea derivatives opens doors to new discoveries in drug development and medicinal applications."

In summary, 3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea;iodide not only exemplifies the complexity of chemical compounds but also highlights the intersection of chemistry and medicine.