1616956-42-3

Basic information

• Product Name: (E)-1-phenyl-3-(p-tolyl)prop-2-yn-1-one O-methyl oxime
• Synonyms: (E)-1-phenyl-3-(p-tolyl)prop-2-yn-1-one O-methyl oxime
• CAS NO: 1616956-42-3
• Molecular Weight: 249.312
• Mol File: 1616956-42-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-1-phenyl-3-(p-tolyl)prop-2-yn-1-one O-methyl oxime(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-phenyl-3-(p-tolyl)prop-2-yn-1-one O-methyl oxime(1616956-42-3)
• EPA Substance Registry System: (E)-1-phenyl-3-(p-tolyl)prop-2-yn-1-one O-methyl oxime(1616956-42-3)

Safety Data

• Hazardous Substances Data: 1616956-42-3(Hazardous Substances Data)

Upstream product

• 93021-70-6 1-phenyl-3-(p-tolyl)prop-2-yn-1-ol 
• 593-56-6 N-methoxylamine hydrochloride 
• 14939-05-0 1-phenyl-3-(4-methylphenyl)prop-2-yn-1-one 
• 100-52-7 benzaldehyde 
• 766-97-2 4-n-methylphenylacetylene 
• 98-88-4 benzoyl chloride 

Downstream Products

• 93752-14-8 3-phenyl-5-(p-tolyl)isothiazole 

Relevant articles and documents

Synthesis of Isoselenazoles and Isothiazoles from Demethoxylative Cycloaddition of Alkynyl Oxime Ethers

A general method for the synthesis of isoselenazoles and isothiazoles has been developed by the base-promoted demethoxylative cycloaddition of alkynyl oxime ethers using the cheap and inactive Se powder and Na2S as selenium and sulfur sources. This transformation features the direct construction of N-, Se-, and S-containing heterocycles through the formation of N-Se/S and C-Se/S bonds in one-pot reactions with excellent functional group tolerance.