4-Bromo-1-ethyl-3,5-dimethyl-1H-pyrazole is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two adjacent nitrogen atoms. The presence of the bromine atom at the 4-position and the ethyl group at the 1-position, along with two methyl groups at the 3 and 5 positions, contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a building block in the synthesis of more complex molecules. The bromine substituent can enhance reactivity, making it useful in various chemical reactions, including nucleophilic substitutions. Additionally, the presence of multiple alkyl groups can influence its solubility and stability in different solvents. As with many pyrazole derivatives, it may exhibit biological activity, warranting further investigation into its pharmacological properties. Safety data should be consulted for handling and usage, as halogenated compounds can pose health risks.

4-bromo-1-ethyl-3,5-dimethyl-1H-pyrazole

51108-51-1: 4-Bromo-1-ethyl-3,5-dimethyl-1H-pyrazole is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two adjacent nitrogen atoms. The presence of the bromine atom at the 4-position and the ethyl group at the 1-position, along with two methyl groups at the 3 and 5 positions, contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a building block in the synthesis of more complex molecules. The bromine substituent can enhance reactivity, making it useful in various chemical reactions, including nucleophilic substitutions. Additionally, the presence of multiple alkyl groups can influence its solubility and stability in different solvents. As with many pyrazole derivatives, it may exhibit biological activity, warranting further investigation into its pharmacological properties. Safety data should be consulted for handling and usage, as halogenated compounds can pose health risks.

CAS 51108-51-1

4-bromo-1-ethyl-3,5-dimethyl-1H-pyrazole

4-Bromo-1-ethyl-3,5-dimethyl-1H-pyrazole

Ref: IN-DA00DCV9

4-bromo-1-ethyl-3,5-dimethyl-1H-pyrazole

Ref: 10-F311817