115504-61-5

Basic information

• Product Name: N'-[(4-fluorophenyl)methylidene]benzeneacylhydrazone
• Synonyms: N'-[(4-fluorophenyl)methylidene]benzeneacylhydrazone
• CAS NO: 115504-61-5
• Molecular Weight: 242.253
• Mol File: 115504-61-5.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: N'-[(4-fluorophenyl)methylidene]benzeneacylhydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: N'-[(4-fluorophenyl)methylidene]benzeneacylhydrazone(115504-61-5)
• EPA Substance Registry System: N'-[(4-fluorophenyl)methylidene]benzeneacylhydrazone(115504-61-5)

Safety Data

• Hazardous Substances Data: 115504-61-5(Hazardous Substances Data)

Upstream product

• 93-58-3 benzoic acid methyl ester 
• 65-85-0 benzoic acid 
• 459-57-4 4-fluorobenzaldehyde 
• 613-94-5 benzoic acid hydrazide 
• 870-63-3 prenyl bromide 
• 106-95-6 allyl bromide 

Downstream Products

• 1092380-85-2 N'-(1-(4-fluorophenyl)propyl)benzohydrazide 
• 1191940-80-3 C₁₈H₁₈ClFN₂O₃ 
• 1242159-24-5 (S)-N'-[1-(4-fluorophenyl)but-3-enyl]benzohydrazide 
• 1242159-32-5 (R)-N'-[1-(4-fluorophenyl)but-3-enyl]benzohydrazide 
• 1620385-48-9 2-(4-fluorophenyl)-5-phenyl-1,3,4-thiadiazole 
• 1392047-81-2 (2S)-2-(4-fluorophenyl)-1,2,3,6-tetrahydropyridine 
• 1392047-74-3 C₁₃H₁₆FN 
• 949021-21-0 (S)-N-[1-(4-fluorophenyl)-3-buten-1-yl]propenamide 
• 949096-30-4 (S)-1-(4-fluorophenyl)-but-3-en-1-amine 

Relevant articles and documents

Synthesis, characterization and biological studies of mononuclear copper(II) complexes with ciprofloxacin and N, O donor ligands

The mixed ligand Cu(II) complexes of ciprofloxacin and N, O donor Schiff bases have been prepared and characterized by physicochemical techniques. In these complexes, ciprofloxacin acts as bidentate deprotonated ligand bound to the metal through the pyrid

Sodium hypochlorite-mediated synthesis of 2,5-disubstituted 1,3,4-oxadiazoles from hydrazides and aldehydes

[Figure not available: see fulltext.] A simple and convenient method for the synthesis of 2,5-disubstituted 1,3,4-oxadiazoles has been developed. Structurally divergent symmetrical and unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles can be obtained in moderate to high yields via NaOCl-mediated oxidative cyclization of N-acylhydrazones, generated in situ from aliphatic and aromatic hydrazides and aldehydes.

Synthesis of amino-diamondoid pharmacophores: Via photocatalytic C-H aminoalkylation

We report a direct C-H aminoalkylation reaction using two light-activated H-atom transfer catalyst systems that enable the introduction of protected amines to native adamantane scaffolds with C-C bond formation. The scope of adamantane and imine reaction partners is broad and deprotection provides versatile amine and amino acid building blocks. Using readily available chiral imines, the enantioselective synthesis of the saxagliptin core and rimantadine derivatives is also described.