Ethyl 2-ethoxy-1-{[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-benzimidazole-7-carboxylate, with the CAS number 856414-35-2, is a complex organic compound characterized by its multi-functional structure. It features a benzimidazole core, which is known for its biological activity, particularly in medicinal chemistry. The presence of an ethoxy group enhances its solubility and potential reactivity, while the trityl-1H-tetrazole moiety may contribute to its pharmacological properties, possibly influencing interactions with biological targets. The biphenyl structure adds to the compound's hydrophobic characteristics, which can affect its bioavailability and distribution in biological systems. This compound is likely to exhibit specific chemical reactivity due to the presence of various functional groups, making it a candidate for further research in drug development or as a chemical probe in biological studies. Its synthesis and characterization would involve standard organic chemistry techniques, and its stability and reactivity would be influenced by the electronic and steric effects of its substituents.

ethyl 2-ethoxy-1-{[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-benzimidazole-7-carboxylate

856414-35-2: Ethyl 2-ethoxy-1-{[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-benzimidazole-7-carboxylate, with the CAS number 856414-35-2, is a complex organic compound characterized by its multi-functional structure. It features a benzimidazole core, which is known for its biological activity, particularly in medicinal chemistry. The presence of an ethoxy group enhances its solubility and potential reactivity, while the trityl-1H-tetrazole moiety may contribute to its pharmacological properties, possibly influencing interactions with biological targets. The biphenyl structure adds to the compound's hydrophobic characteristics, which can affect its bioavailability and distribution in biological systems. This compound is likely to exhibit specific chemical reactivity due to the presence of various functional groups, making it a candidate for further research in drug development or as a chemical probe in biological studies. Its synthesis and characterization would involve standard organic chemistry techniques, and its stability and reactivity would be influenced by the electronic and steric effects of its substituents.

CAS 856414-35-2

ethyl 2-ethoxy-1-{[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-benzimidazole-7-carboxylate

Candesartan N1-Trityl Ethyl Ester

Ref: ST-EA-CP-C50059

Candesartan Cilexetil Impurity 13

Ref: 4Z-C-0129