171359-95-8

Basic information

• Product Name: N'-(2-aminobenzylidene)-4-methylbenzenesulfonohydrazide
• Synonyms: N'-(2-aminobenzylidene)-4-methylbenzenesulfonohydrazide
• CAS NO: 171359-95-8
• Molecular Weight: 289.358
• Mol File: 171359-95-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: N'-(2-aminobenzylidene)-4-methylbenzenesulfonohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N'-(2-aminobenzylidene)-4-methylbenzenesulfonohydrazide(171359-95-8)
• EPA Substance Registry System: N'-(2-aminobenzylidene)-4-methylbenzenesulfonohydrazide(171359-95-8)

Safety Data

• Hazardous Substances Data: 171359-95-8(Hazardous Substances Data)

Upstream product

• 58809-90-8 4-methyl-N'-(2-nitrobenzylidene)-benzenesulfonohydrazide 
• 552-89-6 2-nitro-benzaldehyde 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 529-23-7 o-aminobenzaldehyde 

Downstream Products

• 148291-93-4 (o-aminophenyl)diazomethane 
• 64372-87-8 6-Methylene-2,4-cyclohexadien-1-imine 
• 95-53-4 o-toluidine 
• 13213-88-2 1,4-dihydro-2H-benzo[d][1,3]oxazin-2-one 

Relevant articles and documents

A [4+3] Cycloaddition Reaction of Aza-ortho-quinone Methides with C,N-Cyclic Azomethine Imines for Synthesis of 1,2,4-Triazepines

The base-induced formal [4+3] cycloaddition reaction of C,N-cyclic azomethine imines with aza-ortho-quinone methides, generated in situ, is reported. This protocol provided an efficient method for the synthesis of biologically important 1,2,4-triazepine derivatives, with a wide substrate scope and excellent functional-group tolerance, and it gives moderate to excellent yields under mild conditions. Several of the derivatives exhibited in vitro antitumor activities against the A2780 cell line in a screening of the cancer cell lines HCT-116, H2228, and A2780 by an MTT assay.

Direct Activation of Unmodified Morita-Baylis-Hillman Alcohols through Phosphine Catalysis for Rapid Construction of Three-Dimensional Heterocyclic Compounds

The phosphine-catalyzed tandem annulation reaction of Morita-Baylis-Hillman (MBH) alcohols with azomethine imines has been achieved for the synthesis of biologically important (epoxymethano)-pyrazolo[5,1-b]quinazoline derivatives. A variety of MBH alcohol

Base-promoted domino reaction for the synthesis of 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes

A base-promoted domino reaction to synthesize the 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes has been developed. This strategy provides a simple and beneficial way for the construction of 2,3-disubstituted indole compounds from readily available starting materials under mild conditions.