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3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea

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Identification
Molecular formula
C8H10BrN3S2
CAS number
.
IUPAC name
3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea
State
State

The compound is typically in a solid state at room temperature, exhibiting a crystalline structure.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
335.00
Boiling point (Kelvin)
608.15
General information
Molecular weight
262.16g/mol
Molar mass
262.1600g/mol
Density
1.7340g/cm3
Appearence

This compound generally appears as a crystalline solid. The color can vary depending on the specific synthesis method but it is typically off-white or light yellow.

Comment on solubility

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

The solubility of 3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea can vary significantly based on several factors. Generally, compounds containing isothiourea functional groups often exhibit interesting solubility properties. Here are some key points to consider:

  • Polarity: The presence of polar groups can enhance solubility in polar solvents like water.
  • Hydrogen bonding: Compounds that can form hydrogen bonds are typically more soluble in water.
  • Solvent effects: The choice of solvent is crucial; organic solvents may yield different solubility results than aqueous solutions.
  • Temperature: Solubility may increase with temperature, making it essential to consider the conditions under which solubility is assessed.

In summary, while specific solubility data may be limited, it's essential to conduct experiments to evaluate how factors such as polarity, hydrogen bonding, and temperature influence the solubility of this compound. As the saying goes, "solubility is the key to reactivity" in many chemical processes.

Interesting facts

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

The compound 3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea is a fascinating example of a small organic molecule with intriguing applications in the field of chemistry and biology. Below are some of the notable aspects of this compound:

  • Biological Activity: This compound is known for exhibiting significant biological activity, particularly in the realm of agricultural chemistry. Its derivative nature allows it to function as a potent agent against various microbial organisms.
  • Structural Composition: The unique structure, featuring isothiazole and isothiourea, positions this compound as a valuable target for pharmaceutical synthesis. The presence of the bromo group enhances its electrophilic characteristics, making it a potential lead compound for further studies.
  • Applications: Compounds like this are often investigated for their potential as fungicides or herbicides in crop protection. The integration of isothiazole moieties has seen a rise in interest due to their effectiveness against plant pathogens.
  • Research Frontiers: Ongoing research aims to explore the full spectrum of activities of this compound, examining not just its antimicrobial properties but also its potential anticancer benefits. The versatility of the isothiazole ring lends itself to myriad applications in medicinal chemistry.
  • Mechanism of Action: Understanding how this compound interacts at the molecular level is crucial for developing new therapeutics. Research into its mechanism of action could unveil new pathways and lead to innovations in drug design.

In summary, 3-[(4-bromo-3-methyl-isothiazol-5-yl)methyleneamino]-2-methyl-isothiourea stands out not only for its structural complexity but also for the promise it holds in both agricultural and medicinal chemistry. As scientists continue to delve deeper into its properties, it is poised to become even more significant in future research endeavors.