917956-88-8

Basic information

• Product Name: 4-hydroxy-5-[(3R)-3-hydroxy-3-(2-methylphenyl)propyl]-N,N,1,2-tetramethyl-1H-benzimidazole-6-carboxamide
• Synonyms: 4-hydroxy-5-[(3R)-3-hydroxy-3-(2-methylphenyl)propyl]-N,N,1,2-tetramethyl-1H-benzimidazole-6-carboxamide
• CAS NO: 917956-88-8
• Molecular Weight: 381.475
• Mol File: 917956-88-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-hydroxy-5-[(3R)-3-hydroxy-3-(2-methylphenyl)propyl]-N,N,1,2-tetramethyl-1H-benzimidazole-6-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxy-5-[(3R)-3-hydroxy-3-(2-methylphenyl)propyl]-N,N,1,2-tetramethyl-1H-benzimidazole-6-carboxamide(917956-88-8)
• EPA Substance Registry System: 4-hydroxy-5-[(3R)-3-hydroxy-3-(2-methylphenyl)propyl]-N,N,1,2-tetramethyl-1H-benzimidazole-6-carboxamide(917956-88-8)

Safety Data

• Hazardous Substances Data: 917956-88-8(Hazardous Substances Data)

Upstream product

• 917957-35-8 4-hydroxy-N,N,1,2-tetramethyl-5-[3-(2-methylphenyl)-3-oxopropyl]-1H-benzimidazole-6-carboxamide 
• 917956-90-2 (3R)-7-hydroxy-6-(3-hydroxy-3-o-tolyl-propyl)-2,3-dimethyl-3H-benzoimidazole-5-carboxylic acid dimethylamide (S)-mandelic acid salt 
• 1034771-47-5 5-[(dimethylamino)methyl]-4-hydroxy-N,N,1,2-tetramethyl-1H-benzimidazole-6-carboxamide hydrochloride 
• 713530-51-9 4-(benzyloxy)-6-bromo-1,2-dimethyl-1H-benzimidazole 
• 713530-55-3 4-hydroxy-N,N,1,2-tetramethyl-1H-benzimidazole-6-carboxamide 
• 1034771-32-8 5-((3R)-3-hydroxy-3-(2-methylphenyl)propyl)-4-methoxy-N,N,1,2-tetramethyl-1H-benzimidazole-6-carboxamide 
• 1034771-28-2 4-benzyloxy-5-[(3R)-3-hydroxy-3-(2-methylphenyl)propyl]-N,N,1,2-tetramethyl-1H-benzimidazole-6-carboxamide 

Downstream Products

• 917957-11-0 BYK 405879 
• 1092938-91-4 (8S)-2,3-dimethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydrochromeno[7,8-d]imidazole-5-carboxamide 
• 917956-90-2 (3R)-7-hydroxy-6-(3-hydroxy-3-o-tolyl-propyl)-2,3-dimethyl-3H-benzoimidazole-5-carboxylic acid dimethylamide (S)-mandelic acid salt 

Relevant articles and documents

Synthesis of enantiopure 3,6,7,8-tetrahydrochromeno[7,8-d]imidazoles via asymmetric ketone hydrogenation in the presence of RuCl2[Xyl-P-Phos][DAIPEN]

The asymmetric hydrogenation of complex heterocyclic ketones 1 in the presence of the novel catalyst RuCl2[(S)-Xyl-P-Phos][(S)-DAIPEN] and a base afforded the corresponding alcohols 2 in good enantiomeric purity. The outcome of the reaction dep

INTERMEDIATES AND PROCESS FOR THE PRODUCTION OF 5-SUBSTITUTED TRICYCLIC BENZIMIDAZOLES

The invention relates to compoun ds of the formula 1-a and 1-b, in which R1, R2, R3, Ar and PG have the meanings as indicated in the description. These compounds are valuable intermediates for the preparation of pharmaceutically active compounds.