1372893-10-1

Basic information

• Product Name: (25Z)-N-(1-[2-{3-[(dimethylamino)methyl]-2-methoxyphenyl}-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl]ethylidene)-4-nitrobenzenamine
• CAS NO: 1372893-10-1
• Molecular Weight: 474.519
• Mol File: 1372893-10-1.mol

Chemical Properties

• CAS DataBase Reference: (25Z)-N-(1-[2-{3-[(dimethylamino)methyl]-2-methoxyphenyl}-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl]ethylidene)-4-nitrobenzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: (25Z)-N-(1-[2-{3-[(dimethylamino)methyl]-2-methoxyphenyl}-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl]ethylidene)-4-nitrobenzenamine(1372893-10-1)
• EPA Substance Registry System: (25Z)-N-(1-[2-{3-[(dimethylamino)methyl]-2-methoxyphenyl}-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl]ethylidene)-4-nitrobenzenamine(1372893-10-1)

Safety Data

• Hazardous Substances Data: 1372893-10-1(Hazardous Substances Data)

Upstream product

• 135-02-4 ortho-anisaldehyde 
• 6342-48-9 N'-[(E)-(2-methoxy-phenyl)methylidene]isonicotinohydrazide 
• 1372892-97-1 1-(2-(3-((dimethylamino)methyl)-2-methoxyphenyl)-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl)ethanone 
• 100-01-6 4-nitro-aniline 
• 1372892-96-0 (E)-N'-{3-[(dimethylamino)methyl]-2-methoxybenzylidene}isonicotinoyl hydrazide 
• 54-85-3 isoniazid 

Relevant articles and documents

New oxadiazole derivatives of isonicotinohydrazide in the search for antimicrobial agents: Synthesis and in vitro evaluation

Structural modifications of the front line antitubercular drug isoniazid provide lipophilic adaptations of the drug in which the hydrazide moiety of isoniazid is replaced by 1,3,4-oxadiazole heterocycles to eliminate in vivo acetylation by arylamine N-ace

Synthesis and characterization of (Z)-N-(1-[2-{3-[(dimethylamino)methyl)]- 2-methoxyphenyl}-5-(pyridin-4-YL)-1,3,4-oxadiazol-3(2H)-YL]ethylidene) benzenamine derivatives as potent antifungal agents

In the present study, a series of (Z)-N-(1-[2-{3-[(dimethylamino)methyl)]- 2-methoxyphenyl}-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl]ethylidene) benzenamine derivatives have been synthesized and characterized by IR, 1H NMR and 13C NMR spectra. All the sy