475626-39-2

Basic information

• Product Name: Hydrazinecarbothioamide, 2-[(3-[1,1'-biphenyl]-4-yl-1-phenyl-1H-pyrazol-4-yl)methylene]-
• CAS NO: 475626-39-2
• Molecular Formula: C23H19N5S
• Molecular Weight: 397.503
• Mol File: 475626-39-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Hydrazinecarbothioamide, 2-[(3-[1,1'-biphenyl]-4-yl-1-phenyl-1H-pyrazol-4-yl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarbothioamide, 2-[(3-[1,1'-biphenyl]-4-yl-1-phenyl-1H-pyrazol-4-yl)methylene]-(475626-39-2)
• EPA Substance Registry System: Hydrazinecarbothioamide, 2-[(3-[1,1'-biphenyl]-4-yl-1-phenyl-1H-pyrazol-4-yl)methylene]-(475626-39-2)

Safety Data

• Hazardous Substances Data: 475626-39-2(Hazardous Substances Data)

Upstream product

• 108446-63-5 1-(1-biphenyl-4-yl-ethylidene)-2-phenylhydrazine 
• 79-19-6 thiosemicarbazide 
• 108446-64-6 3-([1,1’-biphenyl]-4-yl)-1-phenyl-1H-pyrazole-4-carboxaldehyde 

Downstream Products

• 1357384-03-2 2-{[[3-(biphenyl-4-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]-hydrazono}-4-phenyl-2,3-dihydrothiazole 
• 1357384-08-7 2-{[[3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]-hydrazono}-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-4-phenyl-2,3-dihydrothiazole 
• 1357384-07-6 2-{2-[2-[[[3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl]ethoxy}ethanol 
• 1357384-06-5 2-{[[3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]-hydrazono}-3-(2-methoxyethyl)-4-phenyl-2,3-dihydrothiazole 
• 1357384-05-4 2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl}acetohydrazide 
• 1357384-04-3 ethyl 2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]hydrazono]-4-phenylthiazol-3(2H)-yl}acetate 
• 1357384-17-8 2,3,4,5-tetra-O-acetyl-D-xylose-2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl}acetohydrazone 
• 1357384-16-7 2,3,4,5,6-penta-O-acetyl-D-mannose-2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl}acetohydrazone 
• 1357384-15-6 2,3,4,5,6-penta-O-acetyl-D-galactose-2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]-hydrazono]-4-phenylthiazol-3(2H)-yl}acetohydrazone 
• 1357384-14-5 D-xylose 2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]hydrazono]-4-phenylthiazol-3(2H)-yl}acetohydrazone 
• 1357384-13-4 D-mannose 2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]hydrazono]-4-phenylthiazol-3(2H)-yl}acetohydrazone 
• 1357384-12-3 D-galactose 2-{2-[[(3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]hydrazono]-4-phenylthiazol-3(2H)-yl}acetohydrazone 
• 1357384-11-2 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 
• 1357384-10-1 2-{2-[[[3-(biphenyl-3-yl)-1-phenyl-1H-pyrazol-4-yl]methylene]hydrazono]-4-phenylthiazol-3(2H)-yl}-N'-(4-chlorobenzylidene)acetohydrazide 

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.