61947-11-3

Basic information

• Product Name: N-((methylsulfonyl)oxy)-4-nitrobenzimidoyl chloride
• Synonyms: N-((methylsulfonyl)oxy)-4-nitrobenzimidoyl chloride
• CAS NO: 61947-11-3
• Molecular Weight: 278.673
• Mol File: 61947-11-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-((methylsulfonyl)oxy)-4-nitrobenzimidoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: N-((methylsulfonyl)oxy)-4-nitrobenzimidoyl chloride(61947-11-3)
• EPA Substance Registry System: N-((methylsulfonyl)oxy)-4-nitrobenzimidoyl chloride(61947-11-3)

Safety Data

• Hazardous Substances Data: 61947-11-3(Hazardous Substances Data)

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 1129-37-9 4-nitrobenzaldehyde oxime 

Downstream Products

• 117804-46-3 C₁₁H₁₃N₃O₅S₃ 
• 117804-47-4 C₁₃H₁₇N₃O₅S₃ 
• 117804-43-0 C₁₃H₁₅N₃O₅S₃ 
• 117804-44-1 C₁₄H₁₇N₃O₅S₃ 
• 117804-45-2 C₁₃H₁₅N₃O₆S₃ 
• 117804-90-7 2,2-Dimethyl-5-[3-(4-nitro-phenyl)-[1,4,2]dithiazol-5-ylidene]-[1,3]dioxane-4,6-dione 
• 117804-88-3 2-[3-(4-Nitro-phenyl)-[1,4,2]dithiazol-5-ylidene]-malonic acid diethyl ester 
• 77585-89-8 1-methyl-3-(4-nitrophenyl)-1-phenylurea 

Relevant articles and documents

One-pot synthesis of trisubstituted ureas from achloroaldoxime O-methanesulfonates and secondary amines

Trisubstituted ureas can be synthesized in a one-pot fashion from bench-stable a-chloroaldoxime Omethanesulfonates and secondary amines under mild reaction conditions. Two practical protocols have been developed to achieve various urea syntheses from both secondary aromatic amines and aliphatic amines.

N-(sulfonyloxy) benzimidoyl halides as bactericidal or fungicidal agents

Agricultural fungicidal compositions based on N-(sulfonyloxy)benzimidoyl halides exhibit a broad spectrum of antifungal activity, particularly against late blight, bean rust and rice blast. The synthesis of representative compounds is described, and the utility of antifungal compositions is exemplified.