1357384-11-2

Basic information

• Product Name: 2-{2-[[[3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl}-N'-(3,4,5-trimethoxybenzylidene)acetohydrazide
• CAS NO: 1357384-11-2
• Molecular Weight: 747.877
• Mol File: 1357384-11-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-{2-[[[3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl}-N'-(3,4,5-trimethoxybenzylidene)acetohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{2-[[[3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl}-N'-(3,4,5-trimethoxybenzylidene)acetohydrazide(1357384-11-2)
• EPA Substance Registry System: 2-{2-[[[3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl}-N'-(3,4,5-trimethoxybenzylidene)acetohydrazide(1357384-11-2)

Safety Data

• Hazardous Substances Data: 1357384-11-2(Hazardous Substances Data)

Upstream product

• 108446-64-6 3-([1,1’-biphenyl]-4-yl)-1-phenyl-1H-pyrazole-4-carboxaldehyde 
• 1357384-05-4 2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl}acetohydrazide 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 1357384-04-3 ethyl 2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]hydrazono]-4-phenylthiazol-3(2H)-yl}acetate 
• 1357384-03-2 2-{[[3-(biphenyl-4-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]-hydrazono}-4-phenyl-2,3-dihydrothiazole 
• 475626-39-2 2-{[3-(biphenyl-4-yl)-1-phenyl-1H-pyrazol-4-yl]methylene}-hydrazinecarbothioamide 

Relevant articles and documents

Synthesis and antimicrobial activity of substituted [(pyrazol-4-yl) methylene]hydrazono-2,3-dihydrothiazoles and their sugar derivatives

A number of new [(pyrazol-4-yl)methylene]hydrazono-2,3-dihydrothiazole derivatives, their sugar hydrazones and N-glycosides were synthesized. Furthermore, N-substituted oxygenated alkyl and hydroxyl derivatives and 1,3,4,-oxadiazoline acyclic nucleoside analogs were prepared. The newly synthesized compounds were tested for their antimicrobial activities and showed moderate to high inhibition activities.