2-(3-Chloropropyl)-1H-benzimidazole is an organic compound characterized by its benzimidazole core, which is a bicyclic structure containing both benzene and imidazole rings. The presence of a 3-chloropropyl substituent enhances its chemical reactivity and solubility properties. This compound typically exhibits moderate polarity due to the presence of the chlorine atom and the alkyl chain, which can influence its interactions in various chemical environments. It may be utilized in pharmaceutical applications, particularly in the development of drugs, due to its potential biological activity. The chlorine substituent can also affect the compound's lipophilicity and bioavailability. Additionally, 2-(3-chloropropyl)-1H-benzimidazole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks. Overall, this compound's unique structure and substituents contribute to its potential utility in medicinal chemistry and related fields.

2-(3-chloropropyl)-1H-benzimidazole

54104-37-9: 2-(3-Chloropropyl)-1H-benzimidazole is an organic compound characterized by its benzimidazole core, which is a bicyclic structure containing both benzene and imidazole rings. The presence of a 3-chloropropyl substituent enhances its chemical reactivity and solubility properties. This compound typically exhibits moderate polarity due to the presence of the chlorine atom and the alkyl chain, which can influence its interactions in various chemical environments. It may be utilized in pharmaceutical applications, particularly in the development of drugs, due to its potential biological activity. The chlorine substituent can also affect the compound's lipophilicity and bioavailability. Additionally, 2-(3-chloropropyl)-1H-benzimidazole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks. Overall, this compound's unique structure and substituents contribute to its potential utility in medicinal chemistry and related fields.

CAS 54104-37-9

2-(3-chloropropyl)-1H-benzimidazole

2-(3-Chloropropyl)-1H-1,3-benzodiazole hydrochloride

Ref: 3D-ECA10437