7757-39-3

Basic information

• Product Name: 4-Pyridinecarboxaldehyde, phenylhydrazone
• CAS NO: 7757-39-3
• Molecular Formula: C12H11N3
• Molecular Weight: 197.239
• Mol File: 7757-39-3.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 4-Pyridinecarboxaldehyde, phenylhydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Pyridinecarboxaldehyde, phenylhydrazone(7757-39-3)
• EPA Substance Registry System: 4-Pyridinecarboxaldehyde, phenylhydrazone(7757-39-3)

Safety Data

• Hazardous Substances Data: 7757-39-3(Hazardous Substances Data)

Upstream product

• 872-85-5 pyridine-4-carbaldehyde 
• 100-63-0 phenylhydrazine 
• 3731-53-1 4-(aminomethyl)pyridine 
• 78-84-2 isobutyraldehyde 
• 6304-16-1 pyridin-4-yl-propan-2-one 
• 100-48-1 pyridine-4-carbonitrile 

Downstream Products

• 109396-53-4 2-piperidino-1-[4]pyridyl-ethanone-phenylhydrazone 
• 108971-67-1 2-morpholino-1-[4]pyridyl-ethanone-phenylhydrazone 
• 104707-33-7 C₁₉H₁₆N₄O 
• 100-48-1 pyridine-4-carbonitrile 
• 7684-30-2 N,N-dimethyl-N'-phenylcarbamimidic chloride 
• 104707-48-4 C₁₃H₁₀ClN₃O 
• 515-42-4 sodium phenylsulfonate 
• 126783-13-9 dichloro(4-pyridinecarbaldehyde phenylhydrazone)(tri-n-propylphosphine)palladium(II) 
• 1223079-74-0 4-ethyl(carbethoxy)amino-5-(pyridin-4-yl)-2-phenyl-2H-1,2,4-triazol-3(4H)-one 
• 1353634-71-5 N-phenylpyridine-4-carbohydrazonoyl chloride 
• 1353634-68-0 4-(4-fluorophenyl)-1-phenyl-3-(pyridine-4-yl)-1H-pyrazol-5-amine 
• 1353634-62-4 5-amino-1-phenyl-3-(pyridine-4-yl)-1H-pyrazole-4-carboxamide 
• 26163-32-6 3-(4-pyridyl)-1,5-diphenylformazan 

Relevant articles and documents

A class of highly effective broad-spectrum plant antimicrobial agentS

The present invention relates to a class of benzohydrazone compounds and synthetic methods thereof and drugs containing the compound thereof and applications thereof. The hydrate compounds involved in the present invention have the advantages of simple structure, easy synthesis, strong antibacterial activity, wide antibacterial spectrum, small toxicity to animals and plants and low composition, and can be used as active ingredients or synergistic ingredients for the development of new high-efficiency broad-spectrum plant antibacterial agents.

Iron-catalyzed aerobic oxidative cleavage of the C-C σ-bond using air as the oxidant: Chemoselective synthesis of carbon chain-shortened aldehydes, ketones and 1,2-dicarbonyl compounds

A simple iron-catalyzed aerobic oxidative C-C σ-bond cleavage of ketones has been developed. Readily available and environmentally benign air is used as the oxidant. This reaction avoids the use of noble metal catalysts or specialized oxidants, chemoselectively yielding carbon chain-shortened aldehydes, ketones and 1,2-dicarbonyl compounds without overoxidation.

Biological properties of heterocyclic pyridinylimines and pyridinylhydrazones

This work describes the synthesis and biological properties of a series of 2- and 4-pyridinylimines and pyridinylhydrazones. All compounds were evaluated in vitro against two species of Leishmania. The antioxidant activity and the toxic effect against mur