34551-63-8

Basic information

• Product Name: (2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-diyl)diethanone
• Synonyms: (2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-diyl)diethanone
• CAS NO: 34551-63-8
• Molecular Weight: 314.341
• Mol File: 34551-63-8.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: (2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-diyl)diethanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-diyl)diethanone(34551-63-8)
• EPA Substance Registry System: (2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-diyl)diethanone(34551-63-8)

Safety Data

• Hazardous Substances Data: 34551-63-8(Hazardous Substances Data)

Upstream product

• 1118-66-7 4-amino-3-penten-2-one 
• 27669-22-3 3-(2-nitrobenzylidene)pentane-2,4-dione 
• 123-54-6 acetylacetone 
• 552-89-6 2-nitro-benzaldehyde 
• 105-45-3 acetoacetic acid methyl ester 
• 60-35-5 acetamide 
• 506-87-6 ammonium carbonate 

Downstream Products

• 94771-72-9 1-Acetyl-2,4,5-trimethyl-3,6-diazaphenanthren 
• 94771-70-7 3,5-Diacetyl-2,6-dimethyl-4-(2-nitrosophenyl)-pyridin 
• 94771-71-8 bis-[2-(3,5-diacetyl-2,6-dimethyl-[4]pyridyl)-phenyl]-diazene-N,N'-dioxide 
• 34551-62-7 3,5-diacetyl-2,6-dimethyl-4-(3'-nitrophenyl)-1,4-dihydropyridine 
• 94398-03-5 3,5-Diacetyl-2,6-dimethyl-4-(2-nitrophenyl)-pyridin 

Relevant articles and documents

Solvent-free efficient one-pot synthesis of Biginelli and Hantzsch compounds catalyzed by potassium phthalimide as a green and reusable organocatalyst

The usage of potassium phthalimide (PPI) for the simple and green one-step multicomponent synthesis of Hantzsch 1,4-dihydropyridines, polyhydroquinolines, 3,4-dihydropyrimidin-2(1H)-ones/thiones, and octahydroquinazolinones under solventless conditions at 120°C is reported. The method is operationally simple, environmentally benign, and has relatively high yields. The other merits of this method include efficient, clean, green, and catalyst reusability.

Synthesis and 3D-QSAR study of 1,4-dihydropyridine derivatives as MDR cancer reverters

A series of symmetrical and unsymmetrical 1,4-dihydropyridines were synthesized by a rapid, single pot microwave irradiation (MWI) based protocol along with conventional approach and characterized by NMR, IR and mass spectroscopic techniques. The compound

Ionic liquid [EMIM]OAc under ultrasonic irradiation towards synthesis of 1,4-DHP's

The ionic liquid 1-ethyl-3-methylimidazole acetate ([EMIM]OAc) was found to be a mild and effective catalyst for the efficient, one-pot, three-component synthesis of 1,4-dihydropyridines from arylalde-hydes, ethylacetoacetate/ acetylacetone and ammonium acetate at room temperature under sonication. The developed method has many advantages, including devoid of harmful catalysts, reacting at room temperature, higher yields in a simple methodology or operational convenience.