6917-08-4

Basic information

• Product Name: N-(4-Methylphenyl)-4-nitrobenzamide
• Synonyms: N-(4-Methylphenyl)-4-nitrobenzamide;AF-936/31272009;ALD-N036573;Benzamide, 4-nitro-N-(4-methylphenyl)-;EU-0069677;Oprea1_097618;Oprea1_376667;ZINC00260683
• CAS NO: 6917-08-4
• Molecular Formula: C₁₄H₁₂N₂O₃
• Molecular Weight: 256.25668
• Mol File: 6917-08-4.mol
• Article Data: 29

Chemical Properties

• Melting Point: 201 °C
• Boiling Point: 354.1±35.0 °C(Predicted)
• Appearance: /
• Density: 1.304±0.06 g/cm3(Predicted)
• PKA: 12.16±0.70(Predicted)
• CAS DataBase Reference: N-(4-Methylphenyl)-4-nitrobenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-Methylphenyl)-4-nitrobenzamide(6917-08-4)
• EPA Substance Registry System: N-(4-Methylphenyl)-4-nitrobenzamide(6917-08-4)

Safety Data

• Hazardous Substances Data: 6917-08-4(Hazardous Substances Data)

Upstream product

• 106-49-0 p-toluidine 
• 62-23-7 4-nitro-benzoic acid 
• 83539-70-2 N-p-nitrobenzoyl-2-phenyliminooxazolidine 
• 13144-36-0 4-Nitro-benzoic-<4-methoxy-benzylcarbonic>-anhydrid 
• 555-16-8 4-nitrobenzaldehdye 
• 5720-05-8 4-methylphenylboronic acid 
• 619-80-7 4-nitrobenzamide 
• 571178-53-5 N-(4-methylphenyl)-4-nitrothiobenzamide 
• 122-04-3 4-nitro-benzoyl chloride 
• 86399-80-6 4-Nitro-N-(4-nitro-benzoyloxy)-N-p-tolyl-benzamide 
• 81724-80-3 C₁₄H₁₂N₂O₃ 
• 69737-96-8 S-(p-nitrophenyl) p-nitrothiobenzoate 
• 28122-84-1 4-nitrothiobenzoic acid S-p-tolyl ester 
• 6631-86-3 S-(p-chlorophenyl) p-nitrothiobenzoate 

Downstream Products

• 860566-25-2 4-nitro-benzoic acid-(4-methyl-2,6-dinitro-anilide) 
• 571178-53-5 N-(4-methylphenyl)-4-nitrothiobenzamide 
• 619-80-7 4-nitrobenzamide 
• 110178-74-0 4-(5-methyl-1H-benzimidazol-2yl)aniline 
• 6393-42-6 4-methyl-2,6-dinitroaniline 
• 36711-56-5 4-(4'-aminobenzamido)benzoic acid 
• 90233-93-5 C₁₆H₁₉N₃O₃S 
• 254966-97-7 6-methyl-2-(4-nitro-phenyl)-4-phenyl-quinazoline 
• 101351-39-7 2-acetoxy-4-(4-nitro-benzoylamino)-toluene 
• 303098-88-6 N-(4-methyl-2-nitrophenyl)-4-nitrobenzamide 
• 19717-14-7 4-(4-Nitrobenzoylamino)-benzoic acid 
• 955-96-4 N-(4-methylphenyl)-4-aminobenzamide 

Relevant articles and documents

Iron-catalyzed cross-coupling of N?methoxy amides and arylboronic acids for the synthesis of N-aryl amides

An efficient iron-catalyzed synthesis of N-aryl amides from N?methoxy amides and arylboronic acids is developed. FeCl3 is used as the sole catalyst for the cross-coupling reaction between N?methoxy amides and arylboronic acids without any other

Green synthetic method of N-arylamides using recyclable cheap metal catalyst

Magnetically separable and reusable Fe/Cu oxide (Fe3O4-Cu2O) nanoparticles were employed as an efficient catalyst for the arylation of benzamide, which was carried out with a range of both arylboronic acid and benzamide to afford N-arylamide in good to excellent yield.

2-phenylpyrimidine compounds, preparation method and medical application

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