5023-82-5

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 932-90-1 Benzaldoxime 
• 698-16-8 benzohydroximoyl chloride 

Downstream Products

• 612-01-1 1-methyl-1,3-diphenylurea 
• 73399-96-9 1-(4-methoxyphenyl)-1-methyl-3-phenylurea 
• 53693-55-3 1-benzyl-1-methyl-3-phenyl urea 
• 117804-41-8 C₁₃H₁₆N₂O₃S₃ 
• 117804-87-2 2-(3-Phenyl-[1,4,2]dithiazol-5-ylidene)-malonic acid diethyl ester 
• 117804-89-4 2,2-Dimethyl-5-(3-phenyl-[1,4,2]dithiazol-5-ylidene)-[1,3]dioxane-4,6-dione 
• 866490-37-1 N-benzyl-N'-n-butyl-N''-phenylguanidine 
• 13134-19-5 1,3-diisopropyl-2-phenylguanidine 
• 1193913-73-3 C₁₉H₃₃N₃ 
• 345229-23-4 C₁₈H₂₁N₃ 
• 79877-53-5 5-methoxy-2-phenyl-1H-benzimidazole 
• 2963-65-7 5-methyl-2-phenyl-1H-1,3-benzimidazole 
• 1104075-59-3 C₁₇H₁₆N₂O₂ 
• 117786-17-1 C₁₃H₁₆N₂O₄S₃ 

Relevant academic research and scientific papers

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.

METHOD FOR THE PREPARATION OF THIADIAZOLES

The present invention relates to processes for preparing protected glyceraldehydes, such as (hydroxy)methanesulfonates. In addition, the invention relates to thiadiazoles, particularly 3-diooxolanyl-thiadiazoles.

Synthesis of α-chloroaldoxime O-methanesulfonates and their use in the synthesis of functionalized benzimidazoles

Three different α-chloroaldoxime O-methanesulfonates were synthesized to investigate their chemical properties. The compounds were found to be stable and were able to be stored at ambient temperature without any precautions. The reactions with anilines we

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.