71512-21-5

Basic information

• Product Name: 2-(2-chlorophenyl)-N-phenylacetamide
• Synonyms: 2-(2-chlorophenyl)-N-phenylacetamide
• CAS NO: 71512-21-5
• Molecular Weight: 245.708
• Mol File: 71512-21-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(2-chlorophenyl)-N-phenylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-chlorophenyl)-N-phenylacetamide(71512-21-5)
• EPA Substance Registry System: 2-(2-chlorophenyl)-N-phenylacetamide(71512-21-5)

Safety Data

• Hazardous Substances Data: 71512-21-5(Hazardous Substances Data)

Upstream product

• 2856-63-5 2-Chlorophenylacetonitrile 
• 62-53-3 aniline 
• 10268-06-1 2-(2-chlorophenyl)acetamide 
• 2444-36-2 2'-chloro-benzeneacetic acid 

Downstream Products

• 723-89-7 1-phenyl-indole-2,3-dione 
• 110487-05-3 {2-[3-(2-Chloro-phenyl)-quinolin-2-ylsulfanyl]-ethyl}-dimethyl-amine 
• 3335-98-6 1-phenyl-1,3-dihydro-indol-2-one 
• 85274-90-4 2-Chloro-3-(2-chloro-phenyl)-quinoline 

Relevant articles and documents

Nitrogen enriched mesoporous organic polymer anchored copper(ii) material: An efficient and reusable catalyst for the synthesis of esters and amides from aromatic systems

A new copper-grafted mesoporous poly-melamine-formaldehyde (Cu-mPMF) has been synthesized from melamine and paraformaldehyde in DMSO medium, followed by grafting of Cu(ii) at its surface. Cu-mPMF has been characterized by elemental analysis, powder XRD, HR TEM, FE-SEM, N2 adsorption study, FT-IR, UV-vis DRS, TGA-DTA, EPR spectroscopy, Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). The Cu-grafted mesoporous material showed very good catalytic activity in methyl esterification of benzylic alcohols and amidation of nitriles. Moreover, the catalyst is easily recoverable and can be reused seven times without appreciable loss of catalytic activity in the above reactions. The highly dispersed and strongly bound Cu(ii) sites in the Cu-grafted mesoporous polymer could be responsible for the observed high activities of the Cu-mPMF catalyst. Due to strong binding with the functional groups of the polymer, no evidence of leached copper from the catalyst during the course of reaction emerged, suggesting true heterogeneity in the catalytic process. This journal is

Microwave-assisted sequential amide bond formation and intramolecular amidation: A rapid entry to functionalized oxindoles

(Chemical Equation Presented) A general method has been developed for the synthesis of N-substituted oxindoles. The two-step process involves initial microwave-assisted amide bond formation between 2-halo-arylacetic acids and various alkylamines and anilines, followed by a palladium-catalyzed intramolecular amidation under aqueous conditions. In the case of alkylamines, the procedure can be carried out as a one-pot process without isolation of the intermediate amide.