248595-18-8

Upstream product

• 1428637-07-3 C₁₀H₁₂ClNO₃ 
• 1428637-20-0 C₉H₈BrNO₃ 

Relevant academic research and scientific papers

Ruthenium-catalyzed intramolecular selective halogenation of O-methylbenzohydroximoyl halides: A new route to halogenated aromatic nitriles

The intramolecular halogenation of O-methylbenzohydroximoyl halides in the presence of a Ru catalyst and the ligand diphenylacetylene afforded halo substituted aromatic nitriles in a highly regioselective manner. Further, substituted nitriles were converted into substituted tetrazole derivatives in the presence of NaN3 and I2.

Oxidative degradation of arylfuro-1,2-oxazoles to arylnitriles by potassium permanganate

Arylfuroisoxazolines are oxidatively degraded to arylnitriles by treatment with a mixture of potassium permanganate and sodium acetate in dry dioxane.