93048-09-0

Upstream product

• 4659-47-6 2,3,6-trichlorobenzaldehyde 
• 2881-01-8 2,3,6-trichloro-benzaldehyde-oxime 

Downstream Products

• 135073-82-4 5-(2,3,6-Trichlorobenzoyl)-2'-deoxyuridine oxime 
• 886967-66-4 ethyl 3-(2,3,6-trichlorophenyl)-4,5-dihydroisoxazole-5-carboxylate 
• 91808-72-9 2,3,6-Trichloro-benzonitrile N-oxide 
• 1235471-10-9 methyl 4,5-dihydro-5-methyl-3-(2,3,6-trichlorophenyl)isoxazole-4-carboxylate 
• 1235471-28-9 3-(2,3,6-trichlorophenyl)isoxazole-5-carboxylic acid 4-bromophenylamide 
• 1235471-27-8 4,5-dihydro-3-(2,3,6-trichlorophenyl)isoxazole-5-carboxylic acid 4-(trifluoromethoxy)phenylamide 
• 1264294-03-2 C₁₂H₈Cl₃NO₃ 
• 1235471-16-5 C₁₀H₄Cl₃NO₃ 
• 4681-11-2 2,5,6-tri-chloro-benzonitrile 
• 886967-71-1 3-(2,3,6-trichlorophenyl)-4,5-dihydroisoxazole-5-carboxylic acid 

Relevant academic research and scientific papers

Synthesis and biological activity of 3-substituted isoxazolecarboxamides

A series of novel 3-substituted isoxazolecarboxamides have been prepared. A key step was 1,3-dipolar cycloaddition of nitrile oxides to α,β-unsaturated esters. Some of these compounds exhibited high fungicidal activities against Alternaria alternata, Botrytis cinerea, Rhizoctonia solani, Fusarium culmorum, and Phytophthora cactorum.

Enantioselective 1,3-dipolar cycloaddition reactions using chiral lanthanide catalysts

(Chemical Equation Presented) Regio- and stereoselective 1,3-dipolar cycloaddition of nitrile oxides to internal 2-pentenols, α,β- unsaturated esters and amides catalyzed by R-(+) BINOL-lanthanide complexes affords corresponding 3-aryl-2-isoxazolines with