85046-00-0

Basic information

• Product Name: Cyanessigsaeure-(4-methoxybenzyliden)-hydrazid
• Synonyms: Cyanessigsaeure-(4-methoxybenzyliden)-hydrazid
• CAS NO: 85046-00-0
• Molecular Weight: 217.227
• Mol File: 85046-00-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyanessigsaeure-(4-methoxybenzyliden)-hydrazid(CAS DataBase Reference)
• NIST Chemistry Reference: Cyanessigsaeure-(4-methoxybenzyliden)-hydrazid(85046-00-0)
• EPA Substance Registry System: Cyanessigsaeure-(4-methoxybenzyliden)-hydrazid(85046-00-0)

Safety Data

• Hazardous Substances Data: 85046-00-0(Hazardous Substances Data)

Upstream product

• 140-87-4 Cyanoacetohydrazide 
• 123-11-5 4-methoxy-benzaldehyde 
• 2286-29-5 ethyl 2-cyano-3-(4-methoxyphenyl)prop-2-enoate 
• 15725-17-4 3-(4-methoxybenzylidene)-2,4-pentanedione 

Downstream Products

• 85046-02-2 α-Cyano-β-(1-pyrenyl)-acrylsaeure-(4-methoxybenzyliden)-hydrazid 
• 52693-87-5 4-methylbenzaldehyde hydrazone 
• 4452-08-8 cyanoketene 
• 184582-44-3 4-Amino-2-thioxo-3-p-tolyl-2,3-dihydro-thiazole-5-carboxylic acid [1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 184582-43-2 4-Amino-3-phenyl-2-thioxo-2,3-dihydro-thiazole-5-carboxylic acid [1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 79388-07-1 1,6-diamino-4-(4-methoxyphenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile 
• 184582-46-5 [4-Amino-5-[1-(4-methoxy-phenyl)-meth-(E)-ylidene-hydrazinocarbonyl]-3-phenyl-3H-thiazol-(2Z)-ylidene]-cyano-acetic acid ethyl ester 
• 184582-45-4 4-amino-2-dicyanomethylidene-5-(4-methoxybenzylidenehydrazinocarbonyl)-3-phenyl-2,3-dihydrothiazole 
• 184582-51-2 6-{[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-amino}-3-phenyl-2-thioxo-2,3-dihydro-6H-thiazolo[4,5-d]pyrimidin-7-one 

Relevant articles and documents

Methylene Components Exchange in the Reaction of Cyanoacetohydrazide with 2-Amino-4-arylbuta-1,3-diene-1,1,3-tricarbonitriles

Abstract: 2-Amino-4-arylbuta-1,3-diene-1,1,3-tricarbonitriles obtained by Knoevenagel condensation between aldehydes and malononitrile dimer reacted with cyanoacetohydrazide in the presence of bases to afford N’-arylidene-2-cyanoacethydrazides instead of

Reaction of α-Cyano-β-aryl Acrylic Acid Ethylesters with Hydrazine, a Retro-Knoevenagel-Reaction

We tried to obtain 4-cyano 5-aryl pyrazolidones-(3) 3a, b and related azomethine imines 4a, b.However the reaction of α-cyano β-aryl acrylic acid ethylesters 2a, b with hydrazine yields the familiar cyano acetic acid arylidene hydrazides 5a, b by cleavage