1722-73-2

Basic information

• Product Name: 4-phenyl-3-buten-2-one O-acetyloxime
• Synonyms: 4-phenyl-3-buten-2-one O-acetyloxime
• CAS NO: 1722-73-2
• Molecular Weight: 203.241
• Mol File: 1722-73-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-phenyl-3-buten-2-one O-acetyloxime(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl-3-buten-2-one O-acetyloxime(1722-73-2)
• EPA Substance Registry System: 4-phenyl-3-buten-2-one O-acetyloxime(1722-73-2)

Safety Data

• Hazardous Substances Data: 1722-73-2(Hazardous Substances Data)

Upstream product

• 2887-98-1 benzalacetone oxime 
• 108-24-7 acetic anhydride 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 75-36-5 acetyl chloride 
• 100-52-7 benzaldehyde 

Relevant articles and documents

Polysubstituted Indole Synthesis via Palladium/Norbornene Cooperative Catalysis of Oxime Esters

Polysubstituted indoles are prevalent in pharmaceuticals, agrochemicals, and organic materials. Presented herein is the fact that polyfunctionalized indoles can be efficiently constructed from easily accessible oxime esters and aryl iodides, involving a palladium/norbornene synergistic synthesis. The reaction is enabled by a unique class of electrophiles in palladium/norbornene cooperative catalysis, which are oxime esters derived from simple ketone. The broad substrate scope and high functional group tolerance could make this method attractive for the synthesis of polysubstituted indoles.

Copper-Catalyzed coupling of oxime acetates with aldehydes: A new strategy for synthesis of pyridines

Copper-catalyzed coupling of oxime acetates with aldehydes offers a new strategy for the synthesis of highly substituted pyridines. This novel method tolerates a wide range of functionality and allows for rapid elaboration of the oxime acetates into a variety of substituted pyridines.