85274-93-7

Basic information

• Product Name: 2-(4-bromophenyl)-N-phenylacetamide
• Synonyms: 2-(4-bromophenyl)-N-phenylacetamide
• CAS NO: 85274-93-7
• Molecular Formula: C₁₄H₁₂BrNO
• Molecular Weight: 290.15518
• Mol File: 85274-93-7.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-bromophenyl)-N-phenylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-bromophenyl)-N-phenylacetamide(85274-93-7)
• EPA Substance Registry System: 2-(4-bromophenyl)-N-phenylacetamide(85274-93-7)

Safety Data

• Hazardous Substances Data: 85274-93-7(Hazardous Substances Data)

Upstream product

• 16532-79-9 4-Bromophenylacetonitrile 
• 66003-76-7 Diphenyliodonium triflate 
• 1122-91-4 4-bromo-benzaldehyde 
• 62-53-3 aniline 
• 79-37-8 oxalyl dichloride 
• 1878-68-8 2-(4-bromophenyl)-acetic acid 
• 100246-20-6 3-(4-bromo-phenyl)-2-hydroxyimino-propionic acid 
• 860190-07-4 3-(4-bromo-phenyl)-2-thioxo-propionic acid 

Downstream Products

• 85274-82-4 3-(4-Bromo-phenyl)-2-chloro-quinoline 
• 364355-72-6 N₁-phenyl-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamide 
• 854372-08-0 N-[[4'-[2-oxo-2-(phenylamino)ethyl][1,1'-biphenyl]-4-yl]sulfonyl]-D-valine 1,1-dimethylethyl ester 
• 110487-13-3 {2-[3-(4-Bromo-phenyl)-quinolin-2-ylsulfanyl]-ethyl}-dimethyl-amine 

Relevant articles and documents

Copper-catalyzed transformation of alkyl nitriles to N -arylacetamide using diaryliodonium salts

This work reports a simple and efficient method for the copper-catalyzed redox-neutral transformation of alkyl nitriles using eco-friendly diaryliodonium salts and leading to N-arylacetamides. The method features high efficiency, broad substrate scope and good functional group tolerance.

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

Non-Lactone Carbocyclic and Heterocyclic Antagonists and Agonists of Bacterial Quorum Sensing

Compounds which modulate quorum sensing in quorum sensing bacteria. Compounds of the invention inhibit quorum sensing and/or activate quorum sensing in various bacteria. Compounds that inhibit quorum sensing are particularly useful for inhibition of detri