33490-01-6

Basic information

• Product Name: Benzamide, 4-nitro-N-(2-nitrophenyl)-
• CAS NO: 33490-01-6
• Molecular Formula: C13H9N3O5
• Molecular Weight: 287.232
• Mol File: 33490-01-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzamide, 4-nitro-N-(2-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 4-nitro-N-(2-nitrophenyl)-(33490-01-6)
• EPA Substance Registry System: Benzamide, 4-nitro-N-(2-nitrophenyl)-(33490-01-6)

Safety Data

• Hazardous Substances Data: 33490-01-6(Hazardous Substances Data)

Upstream product

• 5466-94-4 4-Nitro-N-phenyl-benzimidoyl chloride 
• 15163-59-4 potassium o-nitrobenzoate 
• 619-80-7 4-nitrobenzamide 
• 38430-14-7 N-Phenyl-4-nitro-benzimid-saeurechlorid 
• 1429-05-6 phenyl 4-nitrobenzoate 
• 88-74-4 2-nitro-aniline 
• 122-04-3 4-nitro-benzoyl chloride 

Downstream Products

• 98806-50-9 N-(4-(1H-benzo[d]imidazol-2-yl)phenyl)benzamide 
• 27030-98-4 N-(4-(1H-benzo[d]imidazol-2-yl)phenyl)ethanamide 
• 37632-91-0 2',4',4-trinitrobenzanilide 
• 89844-36-0 2',6',4-trinitrobenzanilide 
• 99137-17-4 1-(2-nitrophenyl)-5-(4-nitrophenyl)tetrazole 
• 67236-55-9 4-nitro-2-(4-nitrophenyl)benzimidazole 
• 51776-70-6 2-(4-nitrophenyl)-2H-benzo[d][1,2,3]triazole 
• 99137-11-8 4-nitro-N-(2-nitro-phenyl)-benzimidoyl chloride 
• 2963-77-1 4-(1H-benzimidazol-2-yl)aniline 

Relevant articles and documents

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.

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

Rearrangement of Imidoyl Nitrates to N-Nitro Amides: an Intramolecular O-to-N Migration of a Nitro Group

Imidoyl nitrates, formed by the reaction of imidoyl chlorides with AgNO3, rearrange via a unimolecular, intramolecular mechanism probably involving homolytic fission of the O-N bond to yield N-nitro amides; migration of the nitro group in N-arylimidoyl nitrates to the ortho- and para-positions of the N-aryl ring does not involve a special ortho-directing effect.