133053-84-6

Basic information

• Product Name: N-(2-methyl-3-nitrophenyl)benzamide
• Synonyms: N-(2-methyl-3-nitrophenyl)benzamide
• CAS NO: 133053-84-6
• Molecular Formula: C₁₄H₁₂N₂O₃
• Molecular Weight: 256.25668
• Mol File: 133053-84-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 316.0±35.0 °C(Predicted)
• Appearance: /
• Density: 1.304±0.06 g/cm3(Predicted)
• PKA: 12.60±0.70(Predicted)
• CAS DataBase Reference: N-(2-methyl-3-nitrophenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-methyl-3-nitrophenyl)benzamide(133053-84-6)
• EPA Substance Registry System: N-(2-methyl-3-nitrophenyl)benzamide(133053-84-6)

Safety Data

• Hazardous Substances Data: 133053-84-6(Hazardous Substances Data)

Upstream product

• 140-29-4 phenylacetonitrile 
• 603-83-8 3-nitro-o-tolylamine 
• 606-20-2 2,6-dinitrotoluene 
• 98-88-4 benzoyl chloride 

Downstream Products

• 87885-88-9 1-methyl-4-nitro-2-phenylindole 
• 1192928-05-4 N-(3-benzamido-2-methylphenylcarbamothioyl)-3,4,5-trimethoxybenzamide 

Relevant articles and documents

Ruthenium-catalyzed oxidative decyanative cross-coupling of acetonitriles with amines in air: A general access to primary to tertiary amides under mild conditions

Catalyzed by Ru and in the presence of air and nucleophiles such as amines or ammonia, activation of the C-CN bond could be easily achieved under mild conditions to produce primary to tertiary amides in good to excellent yields. The use of accessible and functional-group-tolerant starting materials, a cheap, low-loading and recyclable catalyst, ligand-free conditions and excellent product yields are the advantages of the method. Moreover, compared with the Ritter reaction and hydration methods, this novel reaction has more comprehensive application scope.

Conformational studies of tertiary oligo-m-benzanilides and oligo-p-benzanilides in solution

A series of oligo-m- and p-benzanilides were made and their conformations in solution were studied by NMR. In most cases, conformational mixtures were observed as soon as three or more monomers were incorporated into the oligomer. Some crystal structures were obtained, which indicated that helical conformations were adopted in the solid state.

Synthesis of Indoles via Ring Closure of 2-Alkylnitroaniline Derivatives.

A variety of nitroindoles have been prepared from imidate, amidine, and sec-anilide derivatives of 2-alkyl-3- or 5-nitroanilines by a base-induced cyclization promoted by dialkyl oxalates.It is shown that essentially the same procedure also can be used to synthesize the corresponding nitroindole-3-glyoxylates in one simple operation.The synthetic potential is discussed and a mechanism is proposed.