90610-42-7

Basic information

• Product Name: 1-(4-(methylsulfonyl)phenyl)ethan-1-one oxime
• Synonyms: 1-(4-(methylsulfonyl)phenyl)ethan-1-one oxime
• CAS NO: 90610-42-7
• Molecular Weight: 213.257
• Mol File: 90610-42-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(4-(methylsulfonyl)phenyl)ethan-1-one oxime(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-(methylsulfonyl)phenyl)ethan-1-one oxime(90610-42-7)
• EPA Substance Registry System: 1-(4-(methylsulfonyl)phenyl)ethan-1-one oxime(90610-42-7)

Safety Data

• Hazardous Substances Data: 90610-42-7(Hazardous Substances Data)

Upstream product

• 10297-73-1 4-(methanesulfonyl)acetophenone 

Downstream Products

• 1620165-36-7 (Z)-N-(1-(4-(methylsulfonyl)phenyl)-4-(triisopropylsilyl)but-1-en-3-yn-1-yl)acetamide 
• 1417704-56-3 C₁₁H₁₃NO₃S 
• 10297-73-1 4-(methanesulfonyl)acetophenone 
• 1236222-37-9 1-(4-(methylsulfonyl)phenyl)ethanone O-6-(4-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidin-1-yl)-5-methylpyrimidin-4-yl oxime 
• 1190364-43-2 iso-butyl 4-(5-methyl-6-(1-(4-(methylsulfonyl)phenyl)ethylideneaminooxy)pyrimidin-4-yloxy)piperidine-1-carboxylate 
• 1190364-42-1 1-(4-(methylsulfonyl)phenyl)ethanone O-5-methyl-6-(1-(pyrimidin-2-yl)piperidin-4-yloxy)pyrimidin-4-yl oxime 
• 1190364-41-0 tert-butyl 4-(5-methyl-6-(1-(4-(methylsulfonyl)phenyl)ethylideneaminooxy)pyrimidin-4-ylamino)piperidine-1-carboxylate 
• 1190364-40-9 1-(4-(methylsulfonyl)phenyl)ethanone O-6-(1-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidin-4-yloxy)pyridazin-3-yl oxime 
• 1190365-47-9 1-(4-(methylsulfonyl)phenyl)ethanone O-1-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidin-4-yl oxime 
• 1190365-16-2 tert-butyl 4-(2-(1-(4-(methylsulfonyl)phenyl)ethylideneaminooxy)ethoxy)piperidine-1-carboxylate 
• 1190364-39-6 1-(4-(methylsulfonyl)phenyl)ethanone O-6-(1-(3-iso-propyl-1,2,4-oxadiazol-5-yl)piperidin-4-yloxy)-5-methylpyrimidin-4-yl oxime 
• 1190365-46-8 tert-butyl 4-(3-(1-(4-(methylsulfonyl)phenyl)ethylideneaminooxy)propyl)piperidine-1-carboxylate 

Relevant articles and documents

Copper-Catalyzed Three-Component Domino Cyclization for the Synthesis of 4-Aryl-5-(arythio)-2-(trifluoromethyl)oxazoles

A copper-catalyzed oxidative cyclization of oxime, arylthiol, and trifluoroacetic anhydride for the construction of trisubstituted oxazoles has been developed. This transformation combines N-O bond cleavage, C-H functionalization, and intramolecular annulation, providing a practical protocol for the introduction of a trifluoromethyl (-CF3) group at oxazole rings.

Rhodium(iii)-catalyzed olefinic C-H alkynylation of enamides at room temperature

Rh(iii)-catalyzed C-H olefinic alkynylation of enamides for the stereospecific construction of synthetically useful Z-type enynamides is reported. This protocol displays good functionality tolerance and operational simplicity thus providing an alternative synthetic opportunity for the ease of access to specific 1,3-enyne derivatives.