203861-66-9

Basic information

• Product Name: N-(4-chlorobenzylidene)methylamine N-oxide
• Synonyms: N-(4-chlorobenzylidene)methylamine N-oxide
• CAS NO: 203861-66-9
• Molecular Weight: 169.611
• Mol File: 203861-66-9.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: N-(4-chlorobenzylidene)methylamine N-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-chlorobenzylidene)methylamine N-oxide(203861-66-9)
• EPA Substance Registry System: N-(4-chlorobenzylidene)methylamine N-oxide(203861-66-9)

Safety Data

• Hazardous Substances Data: 203861-66-9(Hazardous Substances Data)

Upstream product

• 4229-44-1 N-methylhydroxyamine hydrochloride 
• 104-88-1 4-chlorobenzaldehyde 
• 3717-24-6 4-chlorobenzaldehyde oxime 
• 77-78-1 dimethyl sulfate 
• 191991-29-4 N-p-chlorobenzyl-N-methylhydroxylamine 
• 104-11-0 N-methyl-4-chlorobenzylamine 
• 13114-22-2 N-(4-chlorobenzylidene)methylamine 
• 75-52-5 nitromethane 
• 593-77-1 N-Methylhydroxylamine 

Downstream Products

• 33934-07-5 3-(4-chloro-phenyl)-2,4,4-trimethyl-isoxazolidin-5-one 
• 71504-41-1 3t-(4-chloro-phenyl)-2,4-dimethyl-5-oxo-isoxazolidine-4r-carboxylic acid ethyl ester 
• 33184-79-1 3t-(4-chloro-phenyl)-2-methyl-5-oxo-isoxazolidine-4r-carboxylic acid tert-butyl ester 
• 33997-27-2 3-(4-chloro-phenyl)-2,4-dimethyl-isoxazolidin-5-one 
• 33178-01-7 3-(4-chloro-phenyl)-2-methyl-4-phenyl-isoxazolidin-5-one 
• 74491-24-0 N-(4-chloro-α-cyanobenzylidene)methylamine 
• 1058668-04-4 C₂₁H₂₂ClF₂NO₃S 
• 1245730-36-2 (3S,5S)-5-methyl-3-(4-chlorophenyl)-2-methylisoxazolidine-5-carbaldehyde 

Relevant articles and documents

[3+2] cycloadditions: Part XXXV. Selective cycloadditions of C-(4-chlorophenyl)-N-methyl nitrone to cinnamic acid anilides

[3+2] Cycloadditions of nitrones as three-atom components to alkenes yield isoxazolidine cycloadducts, which on chemical transformations can be converted to bioactive compounds. The [3+2] cycloadditions route thus provides conversion of simple natural pro

Carbamoylation of Azomethine Imines via Visible-Light Photoredox Catalysis

A versatile and robust photocatalytic methodology to install the amide functional group into azomethine imine ions is described. This protocol is distinguished by its broad scope and mild reaction conditions, which are well suited for the preparation of s

A highly diastereoselective [3+3] annulation reaction of aza-oxyallyl cations and nitrones

An efficient synthesis of 1,2,4-oxadiazinan-5-ones via [3+3] cycloaddition of in situ generated aza-oxyallyl cations with nitrones has been developed. The protocol features easy operation, excellent yields, excellent diastereo-control, broad substrate sco