4-Bromo-1H-pyrazole-5-carbothioamide is a heterocyclic organic compound characterized by the presence of a pyrazole ring, which is a five-membered ring containing two nitrogen atoms. The compound features a bromine atom at the 4-position and a carbothioamide functional group at the 5-position, contributing to its reactivity and potential biological activity. The presence of the bromine atom enhances its electrophilic character, making it suitable for various chemical reactions, including nucleophilic substitutions. The carbothioamide group introduces a thiocarbonyl functionality, which can participate in further chemical transformations and may exhibit biological properties, such as antimicrobial or antifungal activity. This compound is of interest in medicinal chemistry and material science due to its unique structural features and potential applications. Its solubility, stability, and reactivity can vary depending on the solvent and conditions, making it important to consider these factors in practical applications. Overall, 4-bromo-1H-pyrazole-5-carbothioamide represents a versatile building block in organic synthesis and drug development.

4-bromo-1H-pyrazole-5-carbothioamide

289504-61-6: 4-Bromo-1H-pyrazole-5-carbothioamide is a heterocyclic organic compound characterized by the presence of a pyrazole ring, which is a five-membered ring containing two nitrogen atoms. The compound features a bromine atom at the 4-position and a carbothioamide functional group at the 5-position, contributing to its reactivity and potential biological activity. The presence of the bromine atom enhances its electrophilic character, making it suitable for various chemical reactions, including nucleophilic substitutions. The carbothioamide group introduces a thiocarbonyl functionality, which can participate in further chemical transformations and may exhibit biological properties, such as antimicrobial or antifungal activity. This compound is of interest in medicinal chemistry and material science due to its unique structural features and potential applications. Its solubility, stability, and reactivity can vary depending on the solvent and conditions, making it important to consider these factors in practical applications. Overall, 4-bromo-1H-pyrazole-5-carbothioamide represents a versatile building block in organic synthesis and drug development.

CAS 289504-61-6

4-bromo-1H-pyrazole-5-carbothioamide

4-bromo-1H-pyrazole-5-carbothioamide

Ref: IN-DA002X65

4-bromo-1H-pyrazole-3-carbothioamide

Ref: 54-OR27436