60672-33-5

Basic information

• Product Name: (E)-4-methyl-N'-(1-(p-tolyl)ethylidene)benzenesulfonohydrazide
• CAS NO: 60672-33-5
• Molecular Weight: 302.397
• Mol File: 60672-33-5.mol
• Article Data: 46

Chemical Properties

• CAS DataBase Reference: (E)-4-methyl-N'-(1-(p-tolyl)ethylidene)benzenesulfonohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-4-methyl-N'-(1-(p-tolyl)ethylidene)benzenesulfonohydrazide(60672-33-5)
• EPA Substance Registry System: (E)-4-methyl-N'-(1-(p-tolyl)ethylidene)benzenesulfonohydrazide(60672-33-5)

Safety Data

• Hazardous Substances Data: 60672-33-5(Hazardous Substances Data)

Usage

General Description

"(E)-4-methyl-N'-(1-(p-tolyl)ethylidene)benzenesulfonohydrazide" is a chemical compound with the molecular formula C16H18N2O2S. It is a hydrazide derivative that is commonly used in various research and industrial applications. (E)-4-methyl-N'-(1-(p-tolyl)ethylidene)benzenesulfonohydrazide has potential applications in the fields of pharmaceuticals, agrochemicals, and materials science. It belongs to the class of organic compounds known as benzene and substituted derivatives, and it is also classified as a naphthalene sulfonamide. (E)-4-methyl-N'-(1-(p-tolyl)ethylidene)benzenesulfonohydrazide may have potential therapeutic properties due to its chemical structure and functional groups, making it a subject of interest for further investigation and development. Additionally, it is important to handle this chemical with care and in accordance with safety protocols due to its potential hazards and risks.

Upstream product

• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 766-97-2 4-n-methylphenylacetylene 
• 122-00-9 para-methylacetophenone 
• 98-59-9 p-toluenesulfonyl chloride 
• 89108-49-6 1-(1-azidovinyl)-4-methyl benzene 

Downstream Products

• 1233239-36-5 1,4-bis(4-methylphenyl)-1H-1,2,3-triazole 
• 22666-07-5 di-p-tolylbutadiyne 
• 1618666-78-6 4-(3-methyl-2-(1-(p-tolyl)vinyl)phenyl)morpholine 
• 327999-85-9 triethyl(1-(p-tolyl)ethyl)silane 
• 65473-90-7 ethyl 2-phenyl-5-(p-tolyl)-1H-pyrrole-3-carboxylate 
• 1198575-39-1 1,6-dimethyl-3,4-diphenyl-isoquinoline 
• 1019011-41-6 4-methyl-3-p-tolyl-1H-pyrazole 

Relevant articles and documents

One-pot synthesis of sulfonylhydrazones from sulfonyl chloride, hydrazine hydrate and vinyl azide in water

A facile and eco-friendly protocol for the synthesis of sulfonylhydrazones from sulfonyl chlorides, hydrazine hydrate and vinyl azides was developed. The unique advantage of this approach is that desired products can be obtained efficiently in water, which meets the requirements of green chemistry and provides good perspectives for the sustainable production of new drug candidate. Also, this reaction proceeded in moderate to good yields with a wide tolerance of functional groups.

Pyrrolo-imidazo[1,2- A[pyridine Scaffolds through a Sequential Coupling of N-Tosylhydrazones with Imidazopyridines and Reductive Cadogan Annulation, Synthetic Scope, and Application

A new strategy for the construction of 3-phenyl-1H-pyrrolo-imidazo[1,2-a]pyridine backbone is described. The reaction starts from the coupling between N-tosylhydrazones and 2-chloro-3-nitroimidazo[1,2-a]pyridines leading to the formation of 3-nitro-2-(ary

Copper(i)-catalyzed benzylation of triazolopyridine through direct C-H functionalization

A general and efficient copper-catalyzed benzylation reaction of triazolopyridine with N-tosylhydrazones was developed. This reaction forms a C(sp2)-C(sp3) bond through cross-coupling, and represents an exceedingly practical method t