1075701-30-2

Basic information

• Product Name: 5-(4-(1H-pyrrol-1-yl)phenyl)-1,3,4-oxadiazole-2-thiol
• Synonyms: 5-(4-(1H-pyrrol-1-yl)phenyl)-1,3,4-oxadiazole-2-thiol
• CAS NO: 1075701-30-2
• Molecular Weight: 243.289
• Mol File: 1075701-30-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5-(4-(1H-pyrrol-1-yl)phenyl)-1,3,4-oxadiazole-2-thiol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-(1H-pyrrol-1-yl)phenyl)-1,3,4-oxadiazole-2-thiol(1075701-30-2)
• EPA Substance Registry System: 5-(4-(1H-pyrrol-1-yl)phenyl)-1,3,4-oxadiazole-2-thiol(1075701-30-2)

Safety Data

• Hazardous Substances Data: 1075701-30-2(Hazardous Substances Data)

Upstream product

• 22106-33-8 4-(1H-pyrrole-1-yl)benzoic acid 
• 62-23-7 4-nitro-benzoic acid 
• 23351-08-8 1-(4-(methyl carboxylate) phenyl) pyrrole 
• 75-15-0 carbon disulfide 
• 112575-84-5 4-(1H-pyrrol-1-yl)benzoic acid hydrazide 

Relevant articles and documents

Utilization of caffeine carbon supported cobalt catalyst in the tandem synthesis of pyrroles from nitroarenes and alkenyl diols

Employing bio-waste caffeine carbon-supported heterogeneous cobalt catalyst, synthesis of various substituted pyrrole derivatives is reported. In this methodology, pyrroles were synthesized through coupling between nitroarenes and alkenyl diols in a tandem manner. Among all the heterogeneous catalysts Co(OAc)2-CC-800 displayed the highest catalytic activity. Preparative scale synthesis of pyrroles and synthesis of anti-tubercular agent 5-(4-(1H-pyrrol-1-yl)phenyl)-1,3,4-oxadiazole-2-thiol revealed the practical applicability of this protocol. Several kinetic experiments and Hammett studies were conducted to understand the probable mechanism and electronic effects on this transformation.