32117-52-5

Basic information

• Product Name: 1-(1-(4-methoxyphenyl)ethylidene)-2-tosylhydrazine
• Synonyms: 1-(1-(4-methoxyphenyl)ethylidene)-2-tosylhydrazine
• CAS NO: 32117-52-5
• Molecular Weight: 318.397
• Mol File: 32117-52-5.mol
• Article Data: 52

Chemical Properties

• CAS DataBase Reference: 1-(1-(4-methoxyphenyl)ethylidene)-2-tosylhydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-(4-methoxyphenyl)ethylidene)-2-tosylhydrazine(32117-52-5)
• EPA Substance Registry System: 1-(1-(4-methoxyphenyl)ethylidene)-2-tosylhydrazine(32117-52-5)

Safety Data

• Hazardous Substances Data: 32117-52-5(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 122948-69-0 4'-methoxyacetophenone (p-tolylsulfonyl)hydrazine 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Downstream Products

• 89619-03-4 2-(4-methoxyphenyl)allylalcohol 
• 75193-06-5 [(CH₃OC₆H₄CCH₂)Co(N₄C₄₄H₂₈)] 
• 110598-51-1 2-(1-(4-methoxyphenyl)vinyl)phenol 
• 31007-06-4 2-(4-methoxyphenyl)propionitrile 
• 22779-05-1 1,4-bis(4-methoxyphenyl)-1,3-butadiyne 
• 1246224-42-9 1-fluoro-2-(4-(4-methoxyphenyl)buta-1,3-diynyl)benzene 
• 116156-19-5 (E)-1-methoxy-4-(4-phenylbutyl-3-en-1-yn-1-yl)benzene 
• 40474-01-9 1-methoxy-4-((4-(trifluoromethyl)phenyl)ethynyl)benzene 

Relevant articles and documents

Copper catalysed alkylation of heteroaryl chloride via migratory insertion of carbenes

Cross-coupling reaction involving Cu catalysed carbene migratory insertion with N-tosylhydrazones as the reaction partner with various substituted cyanuric chloride were studied, which has been recognized as a new type of cross-coupling reaction. Cu-carbe

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