621-06-7

Basic information

• Product Name: 2,N-DIPHENYLACETAMIDE
• Synonyms: 2-PHENYL-N-PHENYLACETAMIDE;2,N-DIPHENYLACETAMIDE;N-PHENYLPHENYLACETAMIDE;2-phenylacetanilide;Glycomide;N,2-Diphenylacetamide;N-Phenylbenzeneacetamide;Phenacetylanilide
• CAS NO: 621-06-7
• Molecular Formula: C₁₄H₁₃NO
• Molecular Weight: 211.26
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 621-06-7.mol
• Article Data: 167

Chemical Properties

• Melting Point: 118 °C
• Boiling Point: 422.7°C at 760 mmHg
• Flash Point: 253.4°C
• Appearance: /
• Density: 1.153g/cm³
• Vapor Pressure: 2.37E-07mmHg at 25°C
• Refractive Index: 1.627
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform (Slightly), Ethyl Acetate (Slightly)
• PKA: 15.00±0.70(Predicted)
• CAS DataBase Reference: 2,N-DIPHENYLACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,N-DIPHENYLACETAMIDE(621-06-7)
• EPA Substance Registry System: 2,N-DIPHENYLACETAMIDE(621-06-7)

Safety Data

• Hazardous Substances Data: 621-06-7(Hazardous Substances Data)

Usage

Safety Profile

Experimental reproductive effects. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

InChI:InChI=1/C14H13NO/c16-14(11-12-7-3-1-4-8-12)15-13-9-5-2-6-10-13/h1-10H,11H2,(H,15,16)

Upstream product

• 62167-00-4 phenylthioacetic acid 
• 103-72-0 phenyl isothiocyanate 
• 103-82-2 phenylacetic acid 
• 62-53-3 aniline 
• 1555-80-2 phenylacetic anhydride 
• 103-80-0 phenylacetyl chloride 
• 19816-85-4 N'-(1,2-diphenylethylidene)-4-methylbenzenesulfonohydrazide 
• 136848-28-7 C₁₇H₂₁NOSi 
• 2078-18-4 trimethylsilyl 2-phenylacetate 
• 1223-44-5 4-nitrophenyl 2-phenylacetate 
• 56-23-5 tetrachloromethane 
• 103-71-9 phenyl isocyanate 
• 71-43-2 benzene 
• 31844-90-3 2-phenyl-acetoacetic acid anilide 

Downstream Products

• 95395-44-1 3-oxo-2-phenyl-propionic acid anilide 
• 19376-80-8 2,N-diphenyl-N'-p-tolyl-acetamidine 
• 37910-56-8 1,4-diphenyl-pyrrolidine-2,3,5-trione 
• 42003-85-0 N-Phenylphenylacetimidsaeure-ethylester 
• 2859-30-5 2-chloro-3-phenyl-quinoline 
• 52910-86-8 N⁴-Phenylacetyl-anthranilamid 
• 55321-98-7 2,6-dimethylbenzamide 
• 3210-15-9 N-phenyl-2,3-diphenylpropanamide 
• 73308-42-6 N-benzyl-N-phenyl-2-phenylacetamide 
• 103-82-2 phenylacetic acid 
• 4765-56-4 glycosminine 

Relevant articles and documents

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Solar and visible-light active nano Ni/g-C3N4photocatalyst for carbon monoxide (CO) and ligand-free carbonylation reactions

In this study, we investigate the amino and alkoxycarbonylation reaction between various substituted aryl halides, benzyl iodides, and iodocyclohexane with different types of amines and alcohols in the absence of carbon monoxide gas and ligands. Similar reactions are carried out at high temperatures, in the presence of appropriate ligands, stoichiometric amounts of bases, and gaseous carbon monoxide, which endanger the health of organic chemists. We present a novel method that does not utilize ligands, bases, gaseous CO, and special conditions. This procedure is a redox reaction carried out by new economic nano Ni/g-C3N4at room temperature and under visible light. Mo(CO)6was used toin situgenerate CO, to resolve the problems caused by the use of CO gas. This protocol has the ability to be used on a gram scale by using a continuous flow reactor.

Exploration of Cu-catalyzed regioselective hydrodehalogenation of o-haloanilides using EtOH as hydrogen source

In present work, we have explored a Cu(acac)2/vasicine-catalyzed regioselective hydrodehalogenation methodology of o-haloanilides using EtOH as hydrogen source and solvent. The catalytic system could selectively dehalogenate 2-Br and 2-I, and features regioselective, efficient and functional group tolerance.