41780-82-9

Basic information

• Product Name: 4-methyl-N'-(1-(4-nitrophenyl)ethylidene)benzenesulfonohydrazide
• Synonyms: 4-methyl-N'-(1-(4-nitrophenyl)ethylidene)benzenesulfonohydrazide
• CAS NO: 41780-82-9
• Molecular Weight: 333.368
• Mol File: 41780-82-9.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: 4-methyl-N'-(1-(4-nitrophenyl)ethylidene)benzenesulfonohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N'-(1-(4-nitrophenyl)ethylidene)benzenesulfonohydrazide(41780-82-9)
• EPA Substance Registry System: 4-methyl-N'-(1-(4-nitrophenyl)ethylidene)benzenesulfonohydrazide(41780-82-9)

Safety Data

• Hazardous Substances Data: 41780-82-9(Hazardous Substances Data)

Upstream product

• 100-19-6 (4-nitrophenyl)ethanone 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 122948-68-9 4'-nitroacetophenone (p-tolylsulfonyl)hydrazine 

Downstream Products

• 1316859-74-1 1-methoxy-4-(1-(4-nitrophenyl)ethyl)benzene 
• 175276-69-4 ethyl 2-methyl-5-(4-nitrophenyl)furan-3-carboxylate 
• 1198575-41-5 1-methyl-6-nitro-3,4-diphenylisoquinoline 
• 6111-97-3 4-(4-nitrophenyl)-1H-1,2,3-triazole 
• 28358-68-1 1-(4-methoxyphenyl)-1-(4-nitrophenyl)ethylene 
• 58896-24-5 1,2-bis(1-(4-nitrophenyl)ethylidene)hydrazine 

Relevant articles and documents

Copper-Catalyzed Regioselective Coupling of Tosylhydrazones and 2-Pyridones: A Strategy for the Production of N-Alkylated Compounds

The highly regioselective N-alkylation reaction of 2-pyridones was achieved through hydrazone chemistry, especially for substrates with bulky secondary alkyl groups. Described herein is a copper-catalyzed coupling reaction of pyridone derivatives with tosylhydrazones.

I2-Promoted [4 + 2] cycloaddition of: In situ generated azoalkenes with enaminones: Facile and efficient synthesis of 1,4-dihydropyridazines and pyridazines

A facile and efficient strategy for the synthesis of 1,4-dihydropyridazines and pyridazines through I2-promoted [4 + 2] cycloaddition of in situ generated azoalkenes with enaminones has been developed. The switch in selectivity is attributed to the judici

Toward a Greener Barluenga-Valdés Cross-Coupling: Microwave-Promoted C-C Bond Formation with a Pd/PEG/H2O Recyclable Catalytic System

A green Barluenga-Valdés cross-coupling reaction for the synthesis of 1,1-diarylethylenes using palladium catalysis has been developed. The new catalytic system based on Pd/Xphos-SO3Na or Pd/MeDavephos-CF3SO3 in PEG/H2O under microwave irradiation was found to be the best conditions for this transformation. The recyclability of the palladium catalyst system was also studied, and it was found to be active over nine runs without significant loss in its activity.