5433-07-8

Basic information

• Product Name: N-(2-acetamido-5-methyl-phenyl)acetamide
• CAS NO: 5433-07-8
• Molecular Formula: C₁₁H₁₄N₂O₂
• Molecular Weight: 206.244
• Mol File: 5433-07-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 443.7°Cat760mmHg
• Flash Point: 191.8°C
• Density: 1.199g/cm³
• CAS DataBase Reference: N-(2-acetamido-5-methyl-phenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-acetamido-5-methyl-phenyl)acetamide(5433-07-8)
• EPA Substance Registry System: N-(2-acetamido-5-methyl-phenyl)acetamide(5433-07-8)

Safety Data

• Hazardous Substances Data: 5433-07-8(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 496-72-0 4-methyl-1,2-diaminobenzene 
• 75-36-5 acetyl chloride 
• 955-98-6 1,2-bis(4-methylphenyl)diazene oxide 
• 612-45-3 4-methyl-2-nitroacetanilide 
• 99-99-0 1-methyl-4-nitrobenzene 
• 127-09-3 sodium acetate 
• 102276-79-9 4,4'-dimethyl-2,3'-dinitro-ONN-azoxybenzene 
• 102276-78-8 4,4'-dimethyl-2-nitro-ONN-azoxybenzene 
• 95-63-6 1,2,4-Trimethylbenzene 
• 53476-34-9 2-amino-4-methylacetanilide 

Downstream Products

• 120209-26-9 2,5-Dimethyl-6-nitrobenzimidazole 

Relevant articles and documents

Co3O4 nanoparticles prepared by oxidative precipitation method: an efficient and reusable heterogeneous catalyst for N-formylation of amines

Abstract: N-formylation of different amines was carried out with formic acid in the presence of the Co3O4 nanoparticles as an efficient, stable heterogeneous catalyst to give the corresponding formamides under solvent-free conditions. This method has advantages over the reported methods such as high yields, mild conditions, easy work-up and short reaction times. The catalyst was characterized by different techniques such as XRD, SEM and FT-IR spectroscopy. Graphical Abstract: [Figure not available: see fulltext.]

NITRO DERIVATIVES OF AROMATIC AZOXY COMPOUNDS. PART I. 2,2'- AND 4,4'-DIMETHYLAZOXYBENZENE NITRATION PRODUCTS

By nitration of 2,2'-dimethylazoxybenzene (1) with concentrated nitric acid under conditions of increasing severity we obtained in succession nitro derivatives having their nitro groups in position: 4; 3',4 and 2,3',4.From 4,4'-dimethylazoxybenzene (2) we obtained similar products with nitro groups in positions: 2,3' (plus 2,6-isomer) and 2,3',6.Trinitro derivatives were obtained also by nitration of dinitro compounds, while tetranitro derivatives: 2,3',4,5' and 2,3',5',6 were obtained by nitrating trinitro compounds (in the presence of phosphoric acid).By reduction with stannous chloride in a strongly acidic medium we obtained, parallel to monocyclic aromatic amines and the conventional benzidine rearrangement products, also 4,4'-dimethyl-2,3'-diaminoazoxybenzene from dinitro derivative 2b, and 3,3'-dimethylbenzidine from mononitro derivative 1a, the latter being quite unexpected.