34559-52-9

Basic information

• Product Name: 2,2-Oxiranedicarbonitrile, 3-(4-nitrophenyl)-
• CAS NO: 34559-52-9
• Molecular Formula: C10H5N3O3
• Molecular Weight: 215.168
• Mol File: 34559-52-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2,2-Oxiranedicarbonitrile, 3-(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Oxiranedicarbonitrile, 3-(4-nitrophenyl)-(34559-52-9)
• EPA Substance Registry System: 2,2-Oxiranedicarbonitrile, 3-(4-nitrophenyl)-(34559-52-9)

Safety Data

• Hazardous Substances Data: 34559-52-9(Hazardous Substances Data)

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 2700-23-4 4-Nitrobenzylidenemalononitrile 

Downstream Products

• 56526-38-6 5-(4-nitro-phenyl)-thiazol-4-one 
• 66702-56-5 3-ethyl-5-(4-nitro-phenyl)-4-oxo-2-phenyl-4,5-dihydro-thiazolium betaine 
• 66702-60-1 2-cyano-5-(4-nitro-phenyl)-4-oxo-3-phenyl-4,5-dihydro-thiazolium betaine 
• 41226-86-2 3-(4-methoxy-phenyl)-2-(4-nitro-phenyl)-4-phenyl-oxazolidine-5,5-dicarbonitrile 
• 41226-89-5 4-(4-chloro-phenyl)-3-(4-methoxy-phenyl)-2-(4-nitro-phenyl)-oxazolidine-5,5-dicarbonitrile 
• 66702-54-3 2,5-bis-(4-nitro-phenyl)-4-oxo-3-phenyl-4,5-dihydro-thiazolium betaine 
• 66702-47-4 2-methyl-5-(4-nitro-phenyl)-4-oxo-3-phenyl-thiazolidine-2-carbonitrile 
• 59208-07-0 5-(4-nitro-phenyl)-4-oxo-2,3-diphenyl-4,5-dihydro-thiazolium betaine 
• 41226-88-4 4-(4-chloro-phenyl)-2-(4-nitro-phenyl)-3-phenyl-oxazolidine-5,5-dicarbonitrile 
• 187804-47-3 bromo-(4-nitro-phenyl)-acetic acid amide 
• 80815-13-0 2-(4-nitrophenyl)[1,3]thiazolo[3,2-a]benzimidazol-3(2H)-one 
• 131602-95-4 2-(4-nitrophenyl)-1,4-benzothiazin-3-one 

Relevant articles and documents

Pyrenediones as versatile photocatalysts for oxygenation reactions with: In situ generation of hydrogen peroxide under visible light

Pyrenediones (PYDs) are efficient photocatalysts for three oxygenation reactions: Epoxidation of electron deficient olefins, oxidative hydroxylation of organoborons, and oxidation of sulfides via in situ generation of H2O2 under visible light irradiation, using oxygen as a terminal oxidant and IPA as a solvent and a hydrogen donor.

Epoxidation of vinyl cyanides by calcium hypochlorite under catalyst- and solvent-free conditions

In this paper, epoxidation of a wide range of alkenes by calcium hypochlorite (Ca(OCl)2) was investigated under catalyst- and solvent-free conditions. It was noticed that the highest yield was achieved with crushing, when the reaction was betwe

Asymmetric Epoxidation of Alkylidenemalononitriles: Key Step for One-Pot Approach to Enantioenriched 3-Substituted Piperazin-2-ones

The first enantioselective epoxidation of readily available alkylidenemalononitriles has been developed by using a multifunctional cinchona derived thiourea as the organocatalyst and cumyl hydroperoxide as the oxidant. A new simple one-pot asymmetric epox