58476-83-8

Upstream product

• 532-55-8 Benzoyl isothiocyanate 
• 98-88-4 benzoyl chloride 
• 58415-38-6 N-(piperidylthiocarbonyl)benzamide 
• 1338831-69-8 C₁₄H₁₈N₂OS 
• 110-89-4 piperidine 
• 102140-71-6 3-(Benzoylamino)-4-methylfurazan 
• 58476-82-7 N-benzoyl-piperidine-1-carboximidic acid chloroamide 
• 1208-07-7 3-trichloromethyl-5-phenyl-1,2,4-oxadiazole 

Relevant academic research and scientific papers

Facile synthesis of 3-aryl/alkylamino 5-aryl/alkyl 1,2,4-oxadiazoles from acylthiourea

Facile and selective synthesis of 3-aryl/alkylamino 5-aryl/alkyl 1,2,4-oxadiazoles starting from N-acylthioureas has been demonstrated. The regio-selectivity is achieved by simply selecting an appropriate base used for the generation of hydroxyl amine fro

PHOTOCHEMICAL BEHAVIOUR OF 1,2,5-OXADIAZOLES - IRRADIATION OF SOME 3-ACYLAMINO-1,2,5-OXADIAZOLES IN THE PRESENCE OF NUCLEOPHILES

The photochemical behaviour of some 3-acylamino-1,2,5-oxadiazoles (furazans) has been investigated.On irradiation at 254 nm in the presence of nucleophiles (ammonia, primary or secondary amines), the photoreaction produced 3-substituted 1,2,3-oxadiazoles in which the substituent at C(3) arises from the used reagent.Some mechanistic considerations are reported.