41214-79-3

Basic information

• Product Name: Benzamide, N-(2,4-dinitrophenyl)-
• CAS NO: 41214-79-3
• Molecular Formula: C13H9N3O5
• Molecular Weight: 287.232
• Mol File: 41214-79-3.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Benzamide, N-(2,4-dinitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(2,4-dinitrophenyl)-(41214-79-3)
• EPA Substance Registry System: Benzamide, N-(2,4-dinitrophenyl)-(41214-79-3)

Safety Data

• Hazardous Substances Data: 41214-79-3(Hazardous Substances Data)

Upstream product

• 93-98-1 N-phenyl benzoyl amide 
• 55-21-0 benzamide 
• 99-65-0 meta-dinitrobenzene 
• 3393-96-2 p-nitrobenzanilide 
• 3493-72-9 N-(2-nitro-phenyl)-benzimidoyl chloride 
• 34918-79-1 N-(4-nitro-phenyl)-benzimidoyl chloride 
• 18039-42-4 5-Phenyl-1H-tetrazole 
• 98-88-4 benzoyl chloride 
• 97-02-9 2,4-Dinitroanilin 
• 65-85-0 benzoic acid 

Downstream Products

• 119-61-9 benzophenone 
• 35825-18-4 N-(2,4-dinitro-phenyl)-benzamidine 
• 64264-33-1 2-phenyl-5-nitrobenzotriazole 
• 72602-77-8 1-(2,4-dinitrophenyl)-5-phenyltetrazole 
• 91358-38-2 tetrabutylammonium salt of 2',4'-dinitrobenzanilide 
• 14760-93-1 N,N'-Dibenzoyl-2,2',4,4'-tetranitro-oxanilid 
• 3601-98-7 N-(2,4-dinitro-phenyl)-benzimidoyl chloride 
• 1767-25-5 2-phenyl-1H-benzo[d]imidazol-5-amine 

Relevant articles and documents

Transition-metal-free mono- or dinitration of protected anilines

An amide-assisted arene nitration is presented, and both mono- and dinitration of protected anilines could be effected by using NaNO2 and NaNO3 as the mono- and bisnitrating agents, respectively. This divergent synthesis is transition-metal- and acid-free, and features a broad substrate scope, low cost, and ortho–para selectivity.

CuSO4-mediated decarboxylative C-N cross-coupling of aromatic carboxylic acids with amides and anilines

CuSO4-mediated decarboxylative C-N cross-coupling of aromatic carboxylic acid with amide has been developed, leading to N-arylamides in modest to excellent yields. Anilines bearing electron-withdrawing substituents could also couple efficiently

Colorimetric detection of cyanide with N-nitrophenyl benzamide derivatives

A series of structurally simple N-nitrophenyl benzamide derivatives have been developed as chemosensors toward cyanide in aqueous environment by taking advantage of the cyanide's strong affinity toward the acyl carbonyl carbon. The high selectivity of these compounds toward CN- makes it a practical system for monitoring CN- concentrations in aqueous samples.