2-(5-Chloro-1H-benzimidazol-2-yl)-ethylamine is a chemical compound characterized by its unique structure, which includes a benzimidazole moiety substituted with a chlorine atom and an ethylamine group. This compound typically exhibits properties associated with heterocyclic compounds, including potential biological activity due to the presence of the benzimidazole ring, which is known for its role in various pharmacological applications. The chlorine substituent can influence the compound's reactivity and solubility, while the ethylamine group may enhance its interaction with biological targets. The compound's molecular structure suggests it may participate in hydrogen bonding and other intermolecular interactions, making it of interest in medicinal chemistry. Additionally, its CAS number, 135875-16-0, allows for easy identification and reference in chemical databases. Overall, this compound may have applications in drug development, particularly in areas related to antimicrobial or anticancer research, although specific biological activities would require further investigation.

2-(5-CHLORO-1H-BENZOIMIDAZOL-2-YL)-ETHYLAMINE

135875-16-0: Akos B006823, 2-Aminoethyl-5(6)-Chloro-Benzimidazole, Art-Chem-Bb B006823, Chembrdg-Bb 4110558, Timtec-Bb Sbb009274, 1H-Benzimidazole-2-ethanamine,5-chloro-(9CI), 2-(5-chloro-1H-benzimidazol-2-yl)ethanamine

[2-(5-chloro-1H-benzimidazol-2-yl)ethyl]amine

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CAS 135875-16-0: 2-(5-CHLORO-1H-BENZOIMIDAZOL-2-YL)-ETHYLAMINE

[2-(5-chloro-1H-benzimidazol-2-yl)ethyl]amine

Ref: 10-F030509

2-(5-CHLORO-1H-BENZOIMIDAZOL-2-YL)-ETHYLAMINE

Ref: IN-DA009AZN

2-(5-Chloro-1H-benzoimidazol-2-yl)ethylamine

Ref: 3D-FC50811