2408-99-3

Basic information

• Product Name: N-(N-acetyl-sulfanilyl)-N'-benzoyl-hydrazine
• CAS NO: 2408-99-3
• Molecular Weight: 333.368
• Mol File: 2408-99-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(N-acetyl-sulfanilyl)-N'-benzoyl-hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(N-acetyl-sulfanilyl)-N'-benzoyl-hydrazine(2408-99-3)
• EPA Substance Registry System: N-(N-acetyl-sulfanilyl)-N'-benzoyl-hydrazine(2408-99-3)

Safety Data

• Hazardous Substances Data: 2408-99-3(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 3989-50-2 4-acetamidobenzenesulfonylhydrazine 
• 613-94-5 benzoic acid hydrazide 
• 121-60-8 p-acetylaminobenzenesulfonyl chloride 

Downstream Products

• 84907-37-9 N-benzoyl-N'-sulfanilyl-hydrazine 

Relevant articles and documents

Synthesis of sulfanilamido-naphthoquinones as potential antituberculous agents

p-Aminobenzoic acid, the acid hydrazides of benzoic acid, salicylic acid and isonicotinic acid, and 4,4'-diaminodiphenyl sulfone were condensed with p-aminobenzenesulfonyl chloride to give the corresponding N1-substituted sulfanilamides. These molecules were then treated with 1,4-naphthoquinone to yield 2-substituted-1,4-naphthoquinones. The partition coefficient for the substituted quinones showed, in some cases, high diffusion rates to the organic phase, benzene, from physiological Tyrode's solution. These compounds are effective in low concentration in dioxane against the human sensitive strain of Mycobacterium tuberculosis H37 Rv. Sulfanilamides obtained from p-aminosalicylic acid and thiosemicarbazide failed to react with 1,4-naphthoquinone. These sulfanilamides also showed high activity against the same Mycobacterium.