22454-71-3

Basic information

• Product Name: Benzoic acid [1-(4-nitro-phenyl)-eth-(E)-ylidene]-hydrazide
• Synonyms: Benzoic acid [1-(4-nitro-phenyl)-eth-(E)-ylidene]-hydrazide
• CAS NO: 22454-71-3
• Molecular Weight: 283.287
• Mol File: 22454-71-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid [1-(4-nitro-phenyl)-eth-(E)-ylidene]-hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid [1-(4-nitro-phenyl)-eth-(E)-ylidene]-hydrazide(22454-71-3)
• EPA Substance Registry System: Benzoic acid [1-(4-nitro-phenyl)-eth-(E)-ylidene]-hydrazide(22454-71-3)

Safety Data

• Hazardous Substances Data: 22454-71-3(Hazardous Substances Data)

Upstream product

• 613-94-5 benzoic acid hydrazide 
• 100-19-6 (4-nitrophenyl)ethanone 

Downstream Products

• 4187-53-5 (S)-1-(p-nitrophenyl)ethylamine 
• 142068-38-0 (S)-1-p-nitrophenyl-1-(2-benzoylhydrazino)ethane 

Relevant articles and documents

Copper catalyzed cyanomethylation reaction of 4-thiazolidinone

An effective copper catalyzed Cross Dehydrogenative Coupling (CDC) reaction of 4-thiazolidinones with acetonitrile has been developed. The described strategy undergoes radical pathway by employing copper, oxidant and easily available acetonitrile as a cya

Asymmetric hydrogenation method of a ketonic compound and derivative

The present invention relates to a process for the asymmetric hydrogenation of a ketonic compound and derivative. The invention relates to the use of optically active metal complexes as catalysts for the asymmetric hydrogenation of a ketonic compound and derivative. The process for the asymmetric hydrogenation of a ketonic compound and derivative is characterized in that the asymmetric hydrogenation of said compound is carried out in the presence of an effective amount of a metal complex comprising as ligand an optically active diphosphine corresponding to one of the following formulae: STR1