6596-69-6

Basic information

• Product Name: N-phenylbenzenesulfonohydrazide
• CAS NO: 6596-69-6
• Molecular Formula: C₁₂H₁₂N₂O₂S
• Molecular Weight: 248.305
• Mol File: 6596-69-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-phenylbenzenesulfonohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenylbenzenesulfonohydrazide(6596-69-6)
• EPA Substance Registry System: N-phenylbenzenesulfonohydrazide(6596-69-6)

Safety Data

• Hazardous Substances Data: 6596-69-6(Hazardous Substances Data)

Upstream product

• 369-57-3 benzenediazonium tetrafluoroborate 
• 7446-09-5 sulfur dioxide 
• 100-63-0 phenylhydrazine 
• 98-09-9 benzenesulfonyl chloride 
• 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 
• 66003-76-7 Diphenyliodonium triflate 

Downstream Products

• 127-63-9 diphenyl sulphone 
• 86-74-8 9H-carbazole 
• 62-53-3 aniline 
• 98-11-3 benzenesulfonic acid 
• 7465-88-5 4-methoxy-N-phenylbenzamide 
• 38554-27-7 N’,N’-diphenylbenzenesulfonyl hydrazide 
• 93-98-1 N-phenyl benzoyl amide 
• 728-90-5 N-(2-nitrophenyl)benzanilide 
• 92-52-4 biphenyl 
• 1256467-34-1 dimethyl 2-(benzenesulfonamido-N-aniline-N-yl)-3-(triphenylphosphoranylidene)butandioate 
• 1256467-35-2 di-tert-butyl 2-(benzenesulfonamido-N-aniline-N-yl)-3-(triphenylphosphoranylidene)butandioate 
• 58791-52-9 benzenesulfonic acid-(N-phenyl-hydrazide); sodium-compound 
• 802869-23-4 benzenesulfonic acid N-phenyl-hydrazide 
• 1212-08-4 S-Phenyl benzenethiosulfonate 

Relevant articles and documents

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.

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