198549-12-1

Basic information

• Product Name: 4-(2-phenyl-1H-imidazol-1-yl)butanenitrile
• Synonyms: 4-(2-phenyl-1H-imidazol-1-yl)butanenitrile
• CAS NO: 198549-12-1
• Molecular Weight: 211.266
• Mol File: 198549-12-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-(2-phenyl-1H-imidazol-1-yl)butanenitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-phenyl-1H-imidazol-1-yl)butanenitrile(198549-12-1)
• EPA Substance Registry System: 4-(2-phenyl-1H-imidazol-1-yl)butanenitrile(198549-12-1)

Safety Data

• Hazardous Substances Data: 198549-12-1(Hazardous Substances Data)

Upstream product

• 143209-16-9 ethyl 2,3-dioxopropanoate 3-hydrazone 
• 791856-59-2 4-(2-phenylimidazol-1-yl)thiobutyramide 
• 670-96-2 2-Phenylimidazole 
• 5332-06-9 4-bromobutanenitrile 

Downstream Products

• 198549-17-6 5,6-diphenyl-3-(3-(2-phenylimidazol-1-yl)propyl)-1,2,4-triazine 
• 1622292-58-3 3-(3-(2-phenyl-1H-imidazol-1-yl)propyl)-5,6-di-p-tolyl-1,2,4-triazine 
• 1622292-59-4 6,7-di-p-tolyl-1 ,2,3,4-tetrahydro-1 ,5-naphthyridine 
• 1671058-41-5 ethyl 7-(6,7-di-p-tolyl-3,4-dihydro-1,5-naphthyridin-1(2H)-yl)heptanoate 
• 1622292-56-1 7-(6,7-di-p-tolyl-3,4-dihydro-1,5-naphthyridin-1(2H)-yl)heptanoic acid 
• 1622292-57-2 4-(2-phenyl-1H-imidazol-1-yl)butanimidhydrazide 
• 791856-46-7 3-(3-(2-phenylimidazol-1-yl)propyl)-5-phenyl-1,2,4-triazine 
• 791856-68-3 6-(4-bromophenyl)-1,2,3,4-tetrahydro-1,5-naphthyridine 
• 791856-69-4 6-(4-methoxyphenyl)-1,2,3,4-tetrahydro-1,5-naphthyridine 
• 791856-65-0 6-phenyl-1,2,3,4-tetrahydro-1,5-naphthyridine 
• 198549-20-1 5,6-dimethyl-3-(3-(2-phenylimidazol-1-yl)propyl)-1,2,4-triazine 
• 198549-21-2 3-(3-(2-phenylimidazol-1-yl)propyl)-1,2,4-triazine 
• 198549-22-3 6,7-diphenyl-1,2,3,4-tetrahydro-1,5-naphthyridine 
• 13993-61-8 1.1,2,3,4-tetrahydro-1,5-naphthyridine 

Relevant articles and documents

IP RECEPTOR AGONIST HETEROCYCLIC COMPOUNDS

The present invention provides heterocyclic derivatives which activate the IP receptor. Activating the IP receptor signaling pathway is useful to treat many forms of PAH, pulmonary fibrosis and exert beneficial effects in fibrotic conditions of various or

Dienophilicity of imidazole in inverse electron demand Diels-Alder reactions; intramolecular reactions with 1,2,4-triazines

Imidazole and 2-phenylimidazole undergo intramolecular cycloadditions with 1,2,4-triazines tethered between an imidazole nitrogen and the triazinyl C3 position with a trimethylene chain to produce tetrahydro-1,5-naphthyridines following loss of N2/s