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Bromothiazole isothiourea

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Identification
Molecular formula
C6H7BrN4S2
CAS number
51939-29-8
IUPAC name
3-[1-(4-bromoisothiazol-3-yl)ethylideneamino]isothiourea
State
State

At room temperature, bromothiazole isothiourea is typically found in a solid state. It is a stable compound that is often handled in solid form during laboratory experiments and analyses.

Melting point (Celsius)
132.00
Melting point (Kelvin)
405.15
Boiling point (Celsius)
278.00
Boiling point (Kelvin)
551.15
General information
Molecular weight
265.14g/mol
Molar mass
265.1410g/mol
Density
1.6000g/cm3
Appearence

This compound typically appears as a crystalline solid with a characteristic color, which may vary from white to light brown depending on the purity and specific form of the compound. The presence of bromine and heterocyclic groups may impart some additional hues.

Comment on solubility

Solubility of 3-[1-(4-bromoisothiazol-3-yl)ethylideneamino]isothiourea

The solubility profile of 3-[1-(4-bromoisothiazol-3-yl)ethylideneamino]isothiourea can be quite intriguing due to its chemical structure. This compound possesses specific functional groups that influence its interaction with solvents.

  • Polarity: The presence of the isothiourea and halogen substituents may enhance solubility in polar solvents, while limiting solubility in nonpolar environments.
  • Hydrogen bonding: The ability of 3-[1-(4-bromoisothiazol-3-yl)ethylideneamino]isothiourea to form hydrogen bonds with water could suggest significant solubility in aqueous environments.
  • Solvent interactions: Its solubility can be affected by the choice of solvent; for instance, it may dissolve better in solvents like methanol or dimethyl sulfoxide (DMSO) than in hydrocarbons.

As a general observation, compounds derived from isothiazole structures often show variable solubility based on their substituent nature. Therefore, it's essential to evaluate the solubility experimentally for definitive insights. As always, the phrase “the solution is in the solvent” holds true when investigating solubility behaviors!

Interesting facts

Interesting Facts About 3-[1-(4-bromoisothiazol-3-yl)ethylideneamino]isothiourea

This unique compound, 3-[1-(4-bromoisothiazol-3-yl)ethylideneamino]isothiourea, belongs to a fascinating class of chemicals known for their diverse applications in medicinal chemistry and agricultural science. Here are some intriguing insights:

  • Biological Activity: The presence of the isothiazole group in this compound makes it an exciting candidate for biological activity. Compounds containing isothiazoles often exhibit significant antimicrobial and antifungal properties, which could make them useful in developing new therapies.
  • Mechanistic Insights: The ethylideneamino moiety in the structure is known to be involved in various biological interactions, potentially inhibiting certain enzyme functions. Researchers are actively studying how this compound interacts with biological systems to design more effective drugs.
  • Pesticide Development: Given its chemical structure, this compound may find applications in the development of new agrochemicals. The ability to combine a potent isothiazole ring with other functional groups allows for the engineering of novel pesticides that target specific pests without harming beneficial organisms.
  • Chemical Versatility: The synthesis of 3-[1-(4-bromoisothiazol-3-yl)ethylideneamino]isothiourea showcases the versatility of isothioureas, which can undergo various chemical modifications to enhance their properties and functions.
  • Research Potential: Ongoing research into this compound may reveal greater insights into its pharmacokinetics and mechanisms of action, opening up possibilities for therapeutic interventions in complex diseases.

As scientists explore the diverse applications of this compound, they are optimistic about its potential to contribute to advancements in medicinal chemistry and sustainable agriculture.