1287686-47-8

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 1574316-80-5 1-(4-nitrophenyl)but-3-en-1-one oxime 
• 106-95-6 allyl bromide 
• 1011-84-3 4-nitrobenzohydroximoyl chloride 
• 1129-37-9 4-nitrobenzaldehyde oxime 

Downstream Products

• 30213-79-7 3-(4-nitro-phenyl)-5-methylisoxazole 
• 1025818-02-3 C₁₀H₁₁BrN₂O 
• 1287686-55-8 C₁₈H₁₄BrF₂N₃O₃ 
• 1287686-77-4 4-(4-nitrophenyl)-2-oxa-3-azabicyclo[3.1.0]hex-3-ene 
• 1287686-78-5 C₁₀H₁₀N₂O 
• 1287686-79-6 C₁₈H₁₃F₂N₃O₃ 
• 1175952-06-3 4-(5-methylisoxazol-3-yl)aniline 
• 1287686-96-7 2,6-difluoro-N-(4-(5-methylisoxazol-3-yl)phenylcarbaphenylcarbamoyl)benzamide 

Relevant academic research and scientific papers

Potassium iodate (KIO 3) as a novel reagent for the synthesis of isoxazolines: evaluation of antimicrobial activity of the products

Abstract : A novel reagent for the synthesis of isoxazolines has been reported. Aryl aldoximes were made to react with alkenes in the presence of KIO 3 as the oxidising agent. This new reagent has been useful as an oxidant in the synthesis of i

General 5-Halomethyl Isoxazoline Synthesis Enabled by Copper-Catalyzed Oxyhalogenation of Alkenes

A general and efficient oxyhalogenation of unsaturated ketoximes has been achieved through copper catalysis with diethyl bromomalonate, N-chlorosuccinimide, and N-iodosuccinimide, yielding 5-chloromethyl, 5-bromomethyl, and 5-iodomethyl isoxazolines in go

CuBr2-promoted intramolecular bromocyclization of N-allylamides and aryl allyl ketone oximes

A new and easy-to-perform route to 2-oxazolines amd isoxazolines was reported. Using CuBr2 as both the bromide source and the reaction promoter, bromocyclization of N-allylamides and allyl ketone oximes proceeded readily, leading to oxazolines

Design, synthesis, and insecticidal evaluation of new benzoylureas containing isoxazoline and isoxazole group

Twenty-two new benzoylphenylureas containing isoxazoline and the isoxazole group were designed and synthesized, and their structures were characterized by 1H NMR and elemental analysis (or HRMS). The larvicidal activities against Oriental armyw

Investigation into the regiochemistry of some isoxazoles derived from 1,3-dipolar cycloaddition of 4-nitrobenzonitrile oxide with some dipolarophiles: A combined theoretical and experimental studies

Reaction of 4-nitrobenzonitrile oxide(2) which was generated in situ with acrylo nitrile (3), methyl methacrylate (4) and allyl bromide (5) as dipolarphile afforded the new 7a, 8a and 9a compounds respectively. Reactivity and regiochemistry of these react