17716-80-2

Basic information

• Product Name: Acetamide, 2-(4-nitrophenoxy)-N-phenyl-
• CAS NO: 17716-80-2
• Molecular Formula: C14H12N2O4
• Molecular Weight: 272.26
• Mol File: 17716-80-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Acetamide, 2-(4-nitrophenoxy)-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, 2-(4-nitrophenoxy)-N-phenyl-(17716-80-2)
• EPA Substance Registry System: Acetamide, 2-(4-nitrophenoxy)-N-phenyl-(17716-80-2)

Safety Data

• Hazardous Substances Data: 17716-80-2(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 100-02-7 4-nitro-phenol 
• 587-65-5 N-chloroacetyl-aniline 
• 1798-11-4 4-nitrophenoxyacetic acid 
• 5625-99-0 N,N'-diphenylphosphorodiamidic chloride 
• 33901-46-1 2-(4-nitrophenoxy)acetonitrile 
• 66003-76-7 Diphenyliodonium triflate 
• 20142-88-5 2-(4-nitrophenoxy)acetyl chloride 

Downstream Products

• 936632-66-5 1-deoxy-1-(6-{4-[(phenylcarbamoyl)methoxy]phenylamino}-9H-purin-9-yl)-N-ethyl-2,3-O-(1-methylethylidene)-β-D-ribofuranuronamide 
• 936632-82-5 1-deoxy-1-(2-chloro-6-{4-[(phenylcarbamoyl)methoxy]phenylamino}-9H-purin-9-yl)-N-ethyl-2,3-O-(1-methylethylidene)-β-D-ribofuranuronamide 
• 118989-62-1 N-(4-nitrophenyl)-N-phenyl-2-chloroacetamide 
• 836-30-6 4-ntrophenyl(phenyl)amine 
• 64485-32-1 2-(4-aminophenoxy)-N-phenylacetamide 

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.

A convenient preparation of N-alkyl and N-arylamines by smiles rearrangement - Synthesis of analogues of diclofenac

Smiles rearrangement of substituted aryloxyacetamides in which oxygen and nitrogen are separated by COCH2 group has been successful even when the aryloxy ring carries weak or no electron withdrawing group. Earlier reports of such reactions involved either strong electron withdrawing groups or a special catalyst. The diphenylamines thus obtained gave analogues of diclofenac in only one case.