53561-17-4

Basic information

• Product Name: O-allyl ether of cyclohexanone oxime
• Synonyms: O-allyl ether of cyclohexanone oxime
• CAS NO: 53561-17-4
• Molecular Weight: 153.224
• Mol File: 53561-17-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: O-allyl ether of cyclohexanone oxime(CAS DataBase Reference)
• NIST Chemistry Reference: O-allyl ether of cyclohexanone oxime(53561-17-4)
• EPA Substance Registry System: O-allyl ether of cyclohexanone oxime(53561-17-4)

Safety Data

• Hazardous Substances Data: 53561-17-4(Hazardous Substances Data)

Upstream product

• 116141-80-1 cyclohexanone oxime prenyl ether 
• 71350-18-0 cyclohexanone oxime O-crotyl ether 
• 100-64-1 cyclohexanone-oxime 
• 106-95-6 allyl bromide 
• 107-05-1 3-chloroprop-1-ene 
• 38945-21-0 O-allylhydroxylamine hydrochloride 
• 108-94-1 cyclohexanone 
• 6542-54-7 O-Allylhydroxylamine 

Downstream Products

• 76046-67-8 [Pd₂(CH(CH₂OCH₃)CH₂ONC(CH₂)5)2Cl₂] 
• 1416449-77-8 C₂₃H₂₅NO₅ 
• 90642-57-2 2-methyl-4,5,6,7-tetrahydro-1H-indole 
• 14006-85-0 3-Methyl-4,5,6,7-tetrahydro-1H-indole 
• 10500-57-9 5,6,7,8-tetrahydroquinoline 
• 100-64-1 cyclohexanone-oxime 
• 4065-80-9 2-methylenecyclohexanol 
• 108-94-1 cyclohexanone 
• 70650-33-8 cyclohexanone O-(1-allyl-2-oxa-1-aza-spiro[4.5]dec-3-ylmethyl)-oxime 

Relevant articles and documents

Oxime ether containing active group and synthesis method thereof

The invention relates to the technical field of organic matter synthesis, in particular to oxime ether containing an active group and a synthesis method thereof, and the oxime ether has a structure asshown in a general formula (I) which is described in th

Synthesis of ketone O-allyloximes and O-propargyloximes in KOH-DMSO system

In reaction of ketone oximes with allyl bromide and propargyl chloride in KOH - DMSO system were obtained in good yield previously unknown ketone O-allyloximes and O-propargyloximes. The reactions are accompanied with minor regeneration of ketones (up to 12%, mainly 1-5%).

O-ALLYL ETHER AS A NEW PROTECTIVE GROUP FOR OXIMES AND ITS PALLADIUM-CATALYZED DEPROTECTION.

Oximes are protected by O-allyl ether formation, and their palladium-catalyzed deallylation using triethylammonium formate as a reductant proceeds smoothly in boiling ethanol under mild conditions offering a good protective method for oximes.