6596-69-6

Upstream product

• 100-63-0 phenylhydrazine 
• 98-09-9 benzenesulfonyl chloride 
• 7446-09-5 sulfur dioxide 
• 66003-76-7 Diphenyliodonium triflate 
• 369-57-3 benzenediazonium tetrafluoroborate 
• 7647-01-0 hydrogenchloride 
• 7732-18-5 water 
• 59-88-1 phenylhydrazine hydrochloride 
• 618-41-7 Benzenesulfinic acid 
• 64-17-5 ethanol 
• 60-29-7 diethyl ether 

Downstream Products

• 618-41-7 Benzenesulfinic acid 
• 7078-86-6 4-Ethoxycarbonylmethyl-1-benzolsulfonyl-2-phenyl-semicarbazid 
• 92-52-4 biphenyl 
• 139-66-2 diphenyl sulfide 
• 127-63-9 diphenyl sulphone 
• 86-74-8 9H-carbazole 
• 62-53-3 aniline 
• 98-11-3 benzenesulfonic acid 
• 1256467-35-2 di-tert-butyl 2-(benzenesulfonamido-N-aniline-N-yl)-3-(triphenylphosphoranylidene)butandioate 
• 1256467-34-1 dimethyl 2-(benzenesulfonamido-N-aniline-N-yl)-3-(triphenylphosphoranylidene)butandioate 
• 7465-88-5 4-methoxy-N-phenylbenzamide 
• 93-98-1 N-phenyl benzoyl amide 
• 728-90-5 N-(2-nitrophenyl)benzanilide 
• 38554-27-7 N’,N’-diphenylbenzenesulfonyl hydrazide 

Relevant academic research and scientific papers

HYDRAZIDE DERIVATIVES AND THEIR SPECIFIC USE AS ANTIBACTERIAL AGENTS BY CONTROLLING ACINETOBACTER BAUMANNII BACTERIUM

The present invention relates to compounds of the following general formula (I): or a pharmaceutically acceptable salt and/or solvate thereof, their use as a drug, in particular as antibacterial agent, notablyforpreventingand/or treating disorders associa

The triple role of rongalite in aminosulfonylation of aryldiazonium tetrafluoroborates: synthesis of N-aminosulfonamides via a radical coupling reaction

A simple and convenient method for N-aminosulfonamide synthesis from the cross-coupling of aryldiazonium tetrafluoroborates and rongalite under metal-free, oxidant-free, and room-temperature conditions is reported. This method does not require an external amine source, with the aryldiazonium tetrafluoroborates participating as both an aryl radical and a potential amine source in the transformation. Mechanistic studies revealed that rongalite could act as a radical initiator, a sulfur dioxide surrogate and a reducing reagent simultaneously in this reaction.

N-PHENYL-N'-PHENOXYCARBONYL-PHENYLSULFONHYDRAZIDE DERIVATIVE AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

The present invention relates to a N-phenyl-N'-phenoxycarbonyl-phenylsulfonhydrazide derivative with excellent inhibitory activity on PGE2 production, a method for preparing the same and a pharmaceutical composition comprising the same as an ac

Visible-Light Photoredox-Catalyzed Aminosulfonylation of Diaryliodonium Salts with Sulfur Dioxide and Hydrazines

A photoredox-catalyzed three-component synthesis of N-aminosulfonamides starting from diaryliodonium salts, hydrazines and sulfur dioxide is reported. This reaction proceeds under mild conditions at room temperature and is driven by visible light. A simple bisulfite salt can be used as a readily available and easy-to-handle sulfur dioxide source. Mechanistic studies support a catalytic photoredox pathway with the diaryliodonium salt as convenient source for aryl radicals. (Figure presented.).

Hit-to-lead optimization of phenylsulfonyl hydrazides for a potent suppressor of PGE2 production: Synthesis, biological activity, and molecular docking study

Preliminary hit-to-lead optimization of a novel series of phenylsulfonyl hydrazide derivatives, which were derived from the high throughput screening hit compound 1 (IC50 = 5700 nM against PGE2 production), for a potent suppressor of

An efficient synthesis of sulfonylhydrazides and sulfonylsemicarbazides by utilizing alumina as a catalyst

Sulfonyl hydrazides and sulfonyl semicarbazides are readily prepared by the reacting of hydrazine derivatives with sulfonyl chlorides in the presence of basic alumina under solvent-free conditions. Reaction of a sulfonyl chloride with t-butylcarbazate, followed by hydrolysis provides the corresponding sulfonyl hydrazides in higher yield and shorter time than previously reported.