2-Chloro-1-ethyl-imidazole is a chemical compound characterized by its imidazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms. This compound features a chloro substituent at the second position and an ethyl group at the first position of the imidazole ring, contributing to its unique reactivity and properties. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the chlorine atom introduces polar characteristics, which can influence its solubility in various solvents, often making it soluble in polar organic solvents. 2-Chloro-1-ethyl-imidazole may exhibit biological activity, making it of interest in pharmaceutical research and development. Its reactivity can be attributed to the imidazole moiety, which can participate in various chemical reactions, including nucleophilic substitutions and coordination with metal ions. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, this compound's unique structure and properties make it a valuable subject of study in organic and medicinal chemistry.

2-chloro-1-ethyl-imidazole

946061-13-8: 2-Chloro-1-ethyl-imidazole is a chemical compound characterized by its imidazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms. This compound features a chloro substituent at the second position and an ethyl group at the first position of the imidazole ring, contributing to its unique reactivity and properties. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the chlorine atom introduces polar characteristics, which can influence its solubility in various solvents, often making it soluble in polar organic solvents. 2-Chloro-1-ethyl-imidazole may exhibit biological activity, making it of interest in pharmaceutical research and development. Its reactivity can be attributed to the imidazole moiety, which can participate in various chemical reactions, including nucleophilic substitutions and coordination with metal ions. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, this compound's unique structure and properties make it a valuable subject of study in organic and medicinal chemistry.

CAS 946061-13-8

2-chloro-1-ethyl-imidazole

2-Chloro-1-ethyl-1H-imidazole

Ref: IN-DA00IIE0

2-Chloro-1-ethyl-1H-imidazole

Ref: 54-OR928703

2-Chloro-1-ethyl-1H-imidazole

Ref: 10-F224252