13211-11-5

Basic information

• Product Name: Benzaldehyde, (phenylmethyl)hydrazone
• CAS NO: 13211-11-5
• Molecular Formula: C14H14N2
• Molecular Weight: 210.279
• Mol File: 13211-11-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, (phenylmethyl)hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, (phenylmethyl)hydrazone(13211-11-5)
• EPA Substance Registry System: Benzaldehyde, (phenylmethyl)hydrazone(13211-11-5)

Safety Data

• Hazardous Substances Data: 13211-11-5(Hazardous Substances Data)

Upstream product

• 3395-76-4 α,α'-azotoluene 
• 555-96-4 Benzylhydrazine 
• 28867-76-7 benzaldehyde benzylidenehydrazone 
• 64-17-5 ethanol 
• 7647-01-0 hydrogenchloride 
• 100-44-7 benzyl chloride 
• 100-52-7 benzaldehyde 
• 100-39-0 benzyl bromide 
• 25370-09-6 dibenzylcarbamyl chloride 
• 85166-50-3 N-Nitroso-N-benzylhydroxylamine Sodium Salt 
• 89970-60-5 C₇H₆ClN₂O₂^(1-)*Na⁽¹⁺⁾ 
• 52147-55-4 3,4-Dibenzyl-1-thia-3,4-diazolidine-2,5-dione 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 17531-58-7 acetic acid-(benzyl-benzylidene-hydrazide) 
• 103280-97-3 diphenyl-acetic acid-(benzyl-benzylidene-hydrazide) 
• 38127-51-4 3-{N-Benzyl-N'-[1-phenyl-meth-(Z)-ylidene]-hydrazino}-5,5-dimethyl-cyclohex-2-enone 
• 7626-68-8 N,N'-dibenzylhydrazine 
• 41555-53-7 3-{N-Benzyl-N'-[1-phenyl-meth-(E)-ylidene]-hydrazino}-cyclohex-2-enone 
• 100-52-7 benzaldehyde 
• 555-96-4 Benzylhydrazine 
• 725-12-2 2,5-bis-(phenyl)-1,3,4-oxadiazole 
• 588-68-1 1,2-di(benzylidene)hydrazine 
• 28386-89-2 2-benzyl-5-phenyl-2H-tetrazole 
• 102002-92-6 benzenesulfonic acid-(benzyl-benzylidene-hydrazide) 
• 1200448-94-7 1-benzyl-3,6-diphenyl-4-tosyl-1,4,5,6-tetrahydro-1,2,4-triazine 
• 38127-58-1 3-(N,N'-Dibenzyl-hydrazino)-5,5-dimethyl-cyclohex-2-enone 
• 41175-17-1 3-<1,2-Dibenzylhydrazino>-2-cyclohexen-1-on 

Relevant articles and documents

THE REACTION OF N,N-DIBENZYLCARBAMOYL CHLORIDE WITH N-NITROSOHYDROXYLAMINE

The action of N,N-dibenzylcarbamoyl chloride (2) on the sodium salt of N-nitrosohydroxylamines (1) in dry acetonitrile at reflux leads to products whose formation may be rationalized in terms of carbamoylation at either oxygen of the bidentate N-nitrosohydroxylamines.

Metal-Free Synthesis of 1,3,4-Oxadiazoles from N′-(Arylmethyl)hydrazides or 1-(Arylmethyl)-2-(arylmethylene)hydrazines

An efficient and versatile metal-free synthesis of 1,3,4-oxadiazoles from N′-(arylmethyl)hydrazides or 1-(arylmethyl)-2-(arylmethylene)hydrazines through oxidative dehydrogenation is reported. A range of 2,5-disubstituted 1,3,4-oxadiazoles were prepared by treating N′-(arylmethyl)hydrazides with (diacetoxyiodo)benzene in acetonitrile or by treating 1-(arylmethyl)-2-(arylmethylene)hydrazines with [bis(trifluoroacetoxy)iodo]benzene in methyl tert-butyl ether. Aldehyde N-acylhydrazones and aldazines were initially generated in situ as intermediates.