63296-54-8

Upstream product

• 1090-32-0 3-phenyl-4-phenylazo-5(4H)-isoxazolinone 
• 69147-39-3 diphenyl-propanetrione 2-phenylhydrazone 
• 62260-73-5 3,5-Diphenyl-4-nitroisoxazoline 
• 100-34-5 benzene diazonium chloride 
• 91816-23-8 3-Phenyl-4-(phenyl-hydrazono)-4H-isoxazole-5-thione 
• 91816-02-3 N-[5-Hydrazono-3-phenyl-isoxazol-(4E)-ylidene]-N'-phenyl-hydrazine 
• 91816-17-0 1-Phenyl-2-(3-phenyl-4-phenylazo-isoxazol-5-ylsulfanyl)-ethanone 
• 91816-19-2 (3-Phenyl-4-phenylazo-isoxazol-5-ylsulfanyl)-acetic acid ethyl ester 
• 91816-21-6 2-(3-Phenyl-4-phenylazo-isoxazol-5-ylsulfanyl)-acetamide 
• 4865-99-0 4-phenylhydrazono-3-phenyl-2-isoxazolin-5-one 
• 36264-17-2 4-phenylhydrazono-3,5-diphenyl-5-hydroxy-2-isoxazoline 
• 72990-91-1 4-nitro-3,5-diphenyl-4,5-dihydro-isoxazole; sodium salt 
• 62-53-3 aniline 

Downstream Products

• 95310-23-9 (2,5-diphenyl-2H-1,2,3-triazol-4-yl)(phenyl)methanone 
• 59349-12-1 3-benzoyl-4,5-bis(methoxycarbonyl)-1-phenylpyrazole 

Relevant academic research and scientific papers

Studies on Arylhydrazonoisoxazolinethiones. Behaviour of 4-Arylhydrazono-3-phenyl-2-isoxazoline-5-thiones Toward Hydrazines, Grignard Reagents and Alkylating Agents

The 4-arylhydrazono-3-phenyl-2-isoxazoline-5-thiones 2 react with hydrazines to yield the 5-hydrazones 3 and 5.The reaction of 2 with Grignard reagent resulted in addition of the reagent to the thiocarbonyl group to yield 7.Treatment of 2 with diazomethan

SYNTHESIS AND PROPERTIES OF 4-ARYLAZO DERIVATIVES OF ISOXAZOLE AND ISOXAZOLINE

4-Arylazo derivatives of isoxazole and isoxazoline are formed in the reaction of the sodium salts of substituted 4-nitroisoxazolines with aromatic diazo compounds in a weakly alkaline or neutral medium in the cold.To judge from the derivatographic data th