5661-50-7

Basic information

• Product Name: N-Phenoxyacetamide
• Synonyms: N-Phenoxyacetamide
• CAS NO: 5661-50-7
• Molecular Formula: C₈H₉NO₂
• Molecular Weight: 151.16
• Mol File: 5661-50-7.mol
• Article Data: 26

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Phenoxyacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Phenoxyacetamide(5661-50-7)
• EPA Substance Registry System: N-Phenoxyacetamide(5661-50-7)

Safety Data

• Hazardous Substances Data: 5661-50-7(Hazardous Substances Data)

Upstream product

• 4846-21-3 O-phenylhydroxylamine 
• 75-36-5 acetyl chloride 
• 98-80-6 phenylboronic acid 
• 64908-64-1 2-phenoxyisoindol-1,3-dione 
• 108-24-7 acetic anhydride 
• 89466-08-0 2-hydroxyphenyl boronic acid 

Downstream Products

• 108-95-2 phenol 
• 13054-95-0 2,3-diphenylbenzofuran 
• 5782-17-2 2,3-bis(4-methoxyphenyl)benzo[b]furan 
• 1224447-47-5 2,3-bis(4-chlorophenyl)benzo[b]furan 
• 4521-08-8 3-methyl-2-phenylbenzofuran 
• 856771-93-2 (3-phenyl-1-benzofuran-2-yl)methanol 
• 263887-30-5 3-(2-phenyl-1-benzofuran)carbinol 
• 2076-36-0 methyl 3-methylbenzofuran-2-carboxylate 
• 587839-41-6 C₁₈H₁₄O₄ 

Relevant articles and documents

An Activity-Based Sensing Fluorogenic Probe for Monitoring Ethylene in Living Cells and Plants

Ethylene (ET) is an important gaseous plant hormone. It is highly desirable to develop fluorescent probes for monitoring ethylene in living cells. We report an efficient RhIII-catalysed coupling of N-phenoxyacetamides to ethylene in the presenc

Synthesis of ortho-phenolic sulfilimines via an intermolecular sulfur atom transfer cascade reaction

To expand the toolbox for the synthesis of ortho-phenolic sulfilimines, sigmatropic rearrangements were introduced to the field of sulfilimine chemistry. Herein we report a N-H sulfenylation/[2,3]-sigmatropic rearrangement cascade reaction. This mild reaction enables commercially available thiols to serve as the sulfenylation reagent and generates water as the sole byproduct. Moreover, the reaction has a wide substrate scope and can be conducted on a gram scale with excellent reaction efficiency.

Cobalt(III)-Catalyzed Intermolecular Carboamination of Propiolates and Bicyclic Alkenes via Non-Annulative Redox-Neutral Coupling

A cobalt(III)-catalyzed, redox-neutral, intermolecular carboamination of propiolates and bicyclic alkenes was developed. This non-annulative coupling strategy features atom economy, high regioselectivity, good yields, and functional groups tolerance. Such a carboamination reaction was applied to modified phenols from the corresponding phenols under mild conditions.