4-(Chloromethyl)-1-trityl-1H-imidazole is a chemical compound characterized by its imidazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms. The presence of a trityl group, which is a triphenylmethyl group, contributes to its stability and lipophilicity, making it useful in various organic synthesis applications. The chloromethyl substituent introduces a reactive site, allowing for further functionalization or coupling reactions. This compound is typically used in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure allows it to participate in nucleophilic substitution reactions, making it versatile in creating more complex molecules. Additionally, the imidazole moiety is known for its biological activity, often found in various natural products and pharmaceuticals, which may enhance the compound's potential applications in drug development. As with many chemical substances, handling should be done with care, following appropriate safety protocols due to the presence of the chloromethyl group, which can be reactive.

4-(chloromethyl)-1-trityl-1H-imidazole

103057-10-9: 4-(Chloromethyl)-1-trityl-1H-imidazole is a chemical compound characterized by its imidazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms. The presence of a trityl group, which is a triphenylmethyl group, contributes to its stability and lipophilicity, making it useful in various organic synthesis applications. The chloromethyl substituent introduces a reactive site, allowing for further functionalization or coupling reactions. This compound is typically used in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure allows it to participate in nucleophilic substitution reactions, making it versatile in creating more complex molecules. Additionally, the imidazole moiety is known for its biological activity, often found in various natural products and pharmaceuticals, which may enhance the compound's potential applications in drug development. As with many chemical substances, handling should be done with care, following appropriate safety protocols due to the presence of the chloromethyl group, which can be reactive.

CAS 103057-10-9

4-(chloromethyl)-1-trityl-1H-imidazole

4-(Chloromethyl)-1-trityl-1H-imidazole

Ref: IN-DA00865C