41097-47-6

Basic information

• Product Name: N,N'-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazine
• Synonyms: N,N'-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazine
• CAS NO: 41097-47-6
• Molecular Weight: 268.315
• Mol File: 41097-47-6.mol
• Article Data: 75

Chemical Properties

• CAS DataBase Reference: N,N'-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazine(41097-47-6)
• EPA Substance Registry System: N,N'-Bis-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazine(41097-47-6)

Safety Data

• Hazardous Substances Data: 41097-47-6(Hazardous Substances Data)

Upstream product

• 6292-71-3 4-methoxybenzaldehyde semicarbazone 
• 103-13-9 1-(4-methoxyphenyl)-4-methyl-1-penten-3-one 
• 75-61-6 dibromodifluoromethane 
• 5953-85-5 p-anisaldehyde hydrazone 
• 5157-08-4 3-methyl-4,5-dihydro-6-oxopyridazine 
• 123-11-5 4-methoxy-benzaldehyde 
• 4334-74-1 4-methoxybenzylidene thiosemicarbazone 
• 105-13-5 4-Methoxybenzyl alcohol 
• 123-08-0 4-hydroxy-benzaldehyde 
• 70565-01-4 3-(2-(4-methoxybenzylidene)hydrazono)indolin-2-one 
• 2365-44-8 3-hydrazonoindolin-2-one 
• 824-94-2 p-methoxybenzyl chloride 
• 140-69-2 4-methoxybenzylhydrazine 
• 33708-60-0 4-methoxy-benzaldehyde-(4-methoxy-benzylhydrazone) 

Downstream Products

• 28231-25-6 meso-hexestrol dimethyl ether 
• 84495-90-9 (3aS,4R,4aR,7aS,8R,8aR)-2,6-Bis-(4-chloro-phenyl)-4,8-bis-(4-methoxy-phenyl)-tetrahydro-2,3b,6,7b-tetraaza-dicyclopenta[a,e]pentalene-1,3,5,7-tetraone 
• 50398-53-3 2,6-di(4-methoxyphenyl)-1,3,5,7-tetraazabicyclo[3.3.0]octane-4,8-dione-3,7-disulfonyl chloride 
• 17453-03-1 2,5-Bis-<4-methoxy-phenyl>-1,3,4-thiadiazol 
• 39122-59-3 meso-2,2'-bis-(4-methoxy-phenyl)-6,6'-diphenyl-[3,3']bi[1,3,5]thiadiazinyl-4,4'-dione 
• 36951-49-2 4-methoxy-benzaldehyde [5-(4-methoxy-benzylidene)-4-oxo-thiazolidin-2-ylidene]-hydrazone 
• 36951-42-5 (2-(4-methoxyphenyl)methylene)hydrazolyl-1,3-thiazolidin-4-one 
• 65655-95-0 3-(4-methoxy-benzylideneamino)-2-(4-methoxy-phenyl)-thiazolidin-4-one 
• 4334-74-1 4-methoxybenzylidene thiosemicarbazone 
• 874-90-8 4-methoxybenzonitrile 
• 4705-34-4 4,4'-dimethoxystilbene 
• 4705-34-4 1,2-bis(4-methoxyphenyl)ethene 

Relevant articles and documents

Ruthenium(ii)-catalysed 1,2-selective hydroboration of aldazines

Herein, an efficient and simple catalytic method for the selective and partial reduction of aldazines using ruthenium catalyst [Ru(p-cymene)Cl2]2 (1) has been accomplished. Under mild conditions, aldazines undergo the addition of pinacolborane in the presence of a ruthenium catalyst, which delivered N-boryl-N-benzyl hydrazone products. Notably, the reaction is highly selective, and results in exclusive mono-hydroboration and desymmetrization of symmetrical aldazines. Mechanistic studies indicate the involvement of in situ formed intermediate [{(η6-p-cymene)RuCl}2(μ-H-μ-Cl)] (1a) in this selective hydroboration.

Synthesis and antimicrobial activity of some new coumarin and dicoumarol derivatives

PTC reaction of coumarin derivative 1 with alkyl halides afforded C4 oxygen alkylation products 2a-d in appreciative yield, whereas with phenyl isothiocyanate gives the C3 addition product 4; also, one-pot three-component PTC reactio

Unprecedented synthesis of symmetrical azines from alcohols and hydrazine hydrate using nickel based NNN-pincer catalyst: An experimental and computational study

Azines are having widespread applications in both industry as well as synthetic chemistry. Thus new catalytic synthetic protocols are desirable as they are greener alternatives than traditional methods of synthesis. Thus, herein a novel earth abundant nickel based NNN-pincer catalyst Ni(BPEA)(Cl2) is synthesized for the first time for the direct transformation of alcohols and hydrazine hydrate into symmetrical azines. This catalytic reaction is accompanied by dehydrogenative coupling of alcohols and hydrazine hydrate and is carried out in presence of a base. Theoretical calculations supported by experimental evidence have been performed for understanding the mechanistic insights of the reaction.