774582-42-2

Basic information

• Product Name: 1H-Benzimidazole-6-carboxylic acid, 4-hydroxy-1,2-dimethyl-5-(3-oxo-3-phenylpropyl)-, ethyl ester
• CAS NO: 774582-42-2
• Molecular Formula: C21H22N2O4
• Molecular Weight: 366.417
• Mol File: 774582-42-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1H-Benzimidazole-6-carboxylic acid, 4-hydroxy-1,2-dimethyl-5-(3-oxo-3-phenylpropyl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazole-6-carboxylic acid, 4-hydroxy-1,2-dimethyl-5-(3-oxo-3-phenylpropyl)-, ethyl ester(774582-42-2)
• EPA Substance Registry System: 1H-Benzimidazole-6-carboxylic acid, 4-hydroxy-1,2-dimethyl-5-(3-oxo-3-phenylpropyl)-, ethyl ester(774582-42-2)

Safety Data

• Hazardous Substances Data: 774582-42-2(Hazardous Substances Data)

Upstream product

• 3433-56-5 1-(1-phenylvinyl)pyrrolidine 
• 921590-18-3 6-dimethylaminomethyl-7-hydroxy-2,3-dimethyl-3H-benzoimidazole-5-carboxylic acid ethyl ester 
• 713530-52-0 ethyl 4-hydroxy-1,2-dimethyl-1H-benzimidazole-6-carboxylate 
• 33797-51-2 eschenmoser's salt 

Downstream Products

• 911048-76-5 1-azetidin-1-yl-1-(8-methoxy-2,3-dimethyl-8-phenyl-3,6,7,8-tetrahydro-chromeno[7,8-d]imidazol-5-yl)-methanone 
• 911048-72-1 8-methoxy-2,3-dimethyl-8-phenyl-3,6,7,8-tetrahydro-chromeno[7,8-d]imidazole-5-carboxylic acid methylamide 
• 911048-71-0 8-methoxy-2,3-dimethyl-8-phenyl-3,6,7,8-tetrahydro-chromeno[7,8-d]imidazole-5-carboxylic acid 
• 911048-74-3 4-hydroxy-5-[(3R)-3-hydroxy-3-phenylpropyl]-N,1,2-trimethyl-1H-benzimidazole-6-carboxamide 
• 911048-73-2 7-hydroxy-2,3-dimethyl-6-(3-oxo-3-phenyl-propyl)-3H-benzoimidazole-5-carboxylic acid methylamide 
• 774582-09-1 7-hydroxy-6-(3-hydroxy-3-phenyl-propyl)-2,3-dimethyl-3H-benzoimidazole-5-carboxylic acid ethyl ester 

Relevant articles and documents

Tetrahydrochromenoimidazoles as potassium-competitive acid blockers (P-CABs): Structure-activity relationship of their antisecretory properties and their affinity toward the hERG channel

Potassium-competitive acid blockers (P-CABs) constitute a new therapeutic option for the treatment of acid-related diseases that are widespread and constitute a significant economical burden. Enantiomerically pure tetrahydrochromenoimidazoles were prepared using the readily available candidate 4 (BYK 405879) as starting material or the Noyori asymmetric reduction of ketones as key reaction. A comprehensive SAR regarding the influence of the 5-carboxamide and the 8-aryl residue on in vitro activity, acid-suppression in the Ghosh Schild rat, and affinity toward the hERG channel was established. In addition, efficacy and duration of the antisecretory action was examined for the most promising target compounds by 24 h pH-metry in the fistula dog and a significantly different SAR was observed as compared to the Ghosh Schild rat. Several tetrahydrochromenoimidazoles were identified that possessed a comparable profile as the candidate 4.