Methylisothiazolinone iodide
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- Molecular formula
- C7H9BrIN4S2
- CAS Number
- null
- IUPAC Name
- 3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea;iodide
- Molecular Weight
- 291.10g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 2.7803g/cm3
Identification
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.