66047-05-0

Basic information

• Product Name: N-(4-BroMoMethylphenyl)acetaMide
• Synonyms: N-(4-BroMoMethylphenyl)acetaMide
• CAS NO: 66047-05-0
• Molecular Formula: C₉H₁₀BrNO
• Molecular Weight: 228.0858
• Mol File: 66047-05-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 379.7°Cat760mmHg
• Flash Point: 183.4°C
• Appearance: /
• Density: 1.5g/cm³
• Vapor Pressure: 5.75E-06mmHg at 25°C
• Refractive Index: 1.616
• CAS DataBase Reference: N-(4-BroMoMethylphenyl)acetaMide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-BroMoMethylphenyl)acetaMide(66047-05-0)
• EPA Substance Registry System: N-(4-BroMoMethylphenyl)acetaMide(66047-05-0)

Safety Data

• Hazardous Substances Data: 66047-05-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H10BrNO/c1-7(12)11-9-4-2-8(6-10)3-5-9/h2-5H,6H2,1H3,(H,11,12)

Upstream product

• 103-89-9 4-Methylacetanilide 
• 64-19-7 acetic acid 
• 7726-95-6 bromine 
• 506-68-3 bromocyane 

Downstream Products

• 66047-06-1 2-[4-(4-acetylamino-benzyl)-piperazin-1-yl]-8-ethyl-5-oxo-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid 
• 1228693-04-6 C₂₅H₂₅F₁₇N₂O₄ 
• 442909-32-2 N-(4-(5-amino-7-(2-furyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-ylmethyl)phenyl)acetamide 
• 74403-07-9 C₂₅H₄₅N₃⁽²⁺⁾*2Br^(1-) 
• 74403-05-7 N-n-cetyl-N,N-dimethyl-N-p-aminobenzylammonium bromide 
• 74403-08-0 C₁₀H₁₅N₃⁽²⁺⁾*2Br^(1-) 
• 74403-06-8 N,N,N-trimethyl-N-p-aminobenzylammonium bromide 
• 945621-58-9 O-benzyl O-(1-O-methyl-2,4,6-tri-O-acetyl-β-D-galactopyranos-3-yl) ((4-acetamidophenyl)methyl)phosphonate 

Relevant articles and documents

Study of 4-acetylaminotoluene ozonation in acetic acid

The reaction of 4-aminotoluene with ozone in acetic acid was studied. It was found that the reaction proceeds at a high rate, giving predominantly tars. The product composition changes after acylation of the amino group: aliphatic peroxides prevailed among the oxidation products and 4-acetylaminobenzoic acid was identified (16%) as well. It was shown that the presence of a catalyst (cobalt(II) acetate) had no substantial effect on the oxidation selectivity for the methyl group (32%) and only the addition of potassium bromide increased the activity of the catalyst; the yield of 4-acetylaminobenzoic acid reached 70%. The mechanism of oxidation in the presence of a cobalt-bromide catalyst explaining the obtained results was discussed.

Halogenolysis of Benzylcobaloximes

The reaction of substituted benzylcobaloximes p-RC6H4Co(dmgH)2-Py (R=OMe, NHCOCH3 and NMe2) and m-RC6H4CH2Co(dmgH)2Py (R=Me, OMe) with halogens (Cl2 and Br2) in chloroform under nitrogen forms ring substituted organic and organometallic products.