251901-68-5

Basic information

• Product Name: 1-(2-furyl)-3-(2-nitrophenyl)-2-propen-1-one
• Synonyms: 1-(2-furyl)-3-(2-nitrophenyl)-2-propen-1-one
• CAS NO: 251901-68-5
• Molecular Weight: 243.219
• Mol File: 251901-68-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-(2-furyl)-3-(2-nitrophenyl)-2-propen-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-furyl)-3-(2-nitrophenyl)-2-propen-1-one(251901-68-5)
• EPA Substance Registry System: 1-(2-furyl)-3-(2-nitrophenyl)-2-propen-1-one(251901-68-5)

Safety Data

• Hazardous Substances Data: 251901-68-5(Hazardous Substances Data)

Upstream product

• 1192-62-7 1-(2-furyl)-1-ethanone 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 1451012-01-3 C₁₃H₁₁NO₂ 
• 1416738-60-7 C₁₃H₁₁N₃O 
• 178625-17-7 3-(2-furyl)-5-(2-nitrophenyl)pyrazole 
• 1416738-66-3 4,5-dihydro-3-(2-furyl)-5-(2-nitrophenyl)-1H-pyrazole 
• 1361014-93-8 3-(furan-2-yl)-5-(2-nitrophenyl)-1-phenyl-4,5-dihydro-1H-pyrazole 
• 1290605-03-6 1-(3-(furan-2-yl)-5-(2-nitrophenyl)-4,5-dihydro-1H-pyrazol-1-yl)ethanone 

Relevant articles and documents

Synthesis and In Vitro Antifungal Evaluation of 1,3,5-Trisubstituted-2-Pyrazoline Derivatives

Pyrazolines, the well-known five-membered nitrogen-containing heterocyclic compounds, have received considerable interests in the fields of medicinal and agricultural chemistry because of their broad spectrum of biological activities. To discover more pot

Tandem Cyclization?Annulation of α-Acidic Isocyanides with 2-Methyleneaminochalcones: Synthesis of Pyrrolo[2,3-c]quinoline Derivatives

Tandem cyclization-annulation of tosylmethyl isocyanide and isocyanoacetate with 2-methyleneaminochalcones as aza-1,5-dielectrophiles has been successfully developed. These domino transformations feature simultaneous formation of three bonds and two rings

Organocatalyzed aerobic oxidative Robinson-type annulation of 2-isocyanochalcones: expedient synthesis of phenanthridines

A DBU-catalyzed aerobic oxidative Robinson annulation of 2-isocyanochalcones with active methylene ketones was developed for the expedient synthesis of phenanthridines in high to excellent yields. This unprecedented multistep domino reaction represents a