154255-39-7

Basic information

• Product Name: N’-((2-chloroquinolin-3-yl)methylene)isonicotinohydrazide
• Synonyms: N’-((2-chloroquinolin-3-yl)methylene)isonicotinohydrazide
• CAS NO: 154255-39-7
• Molecular Weight: 309.755
• Mol File: 154255-39-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N’-((2-chloroquinolin-3-yl)methylene)isonicotinohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N’-((2-chloroquinolin-3-yl)methylene)isonicotinohydrazide(154255-39-7)
• EPA Substance Registry System: N’-((2-chloroquinolin-3-yl)methylene)isonicotinohydrazide(154255-39-7)

Safety Data

• Hazardous Substances Data: 154255-39-7(Hazardous Substances Data)

Upstream product

• 54-85-3 isoniazid 
• 73568-25-9 2-chloro-3-quinoline carboxaldehyde 
• 103-84-4 Acetanilid 
• 613-94-5 benzoic acid hydrazide 

Downstream Products

• 1397263-11-4 C₂₄H₁₇Cl₂N₅O 
• 1397263-12-5 C₂₄H₁₇Cl₂N₅O 
• 1397263-14-7 C₂₄H₁₇ClN₆O₃ 
• 1397263-15-8 C₂₄H₁₇ClN₆O₃ 
• 1397263-16-9 C₂₄H₁₇ClN₆O₃ 
• 1397263-17-0 C₂₅H₂₀ClN₅O₂ 
• 1397263-18-1 C₂₅H₂₀ClN₅O₂ 
• 1397263-19-2 C₂₅H₂₀ClN₅O₂ 
• 1397263-21-6 C₂₄H₁₇ClFN₅O 
• 1397263-22-7 C₂₄H₁₇ClFN₅O 
• 1397263-13-6 4-chloro-N-(1-(2-(2-chloroquinolin-3-yl)-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl)ethylidene)aniline 
• 1397263-23-8 3-chloro-1-(2-chlorophenyl)-4-(2-(2-chloroquinolin-3-yl)-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl)-4-methylazetidin-2-one 
• 1397263-24-9 3-chloro-1-(3-chlorophenyl)-4-(2-(2-chloroquinolin-3-yl)-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl)-4-methylazetidin-2-one 
• 1397263-25-0 3-chloro-1-(4-chlorophenyl)-4-(2-(2-chloroquinolin-3-yl)-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl)-4-methylazetidin-2-one 

Relevant articles and documents

Synthesis, characterization, and antimicrobial evaluation of quinoline-oxadiazole-based azetidinone derivatives

A series of 3-chloro-1-(aryl)-4-(2-(2-chloroquinolin-3-yl)-5-(pyridin-4-yl) -1,3,4-oxadiazol-3(2H)-yl)-4-ethyl-azetidin-2-ones (5a-l) have been synthesized and characterized by IR, 1H NMR, and13C NMR. Synthesized compounds were screened for their antimicrobial activity against different strains of bacteria (E. coli, P. aeruginosa, S. aureus, S. pyogenes, C. albicans, A. niger, and A. clavatus). On the basis of statistical analysis, it has been observed that compounds had significant correlations.

Synthesis and in vivo anticonvulsant evaluation of 2-chloroquinolinyl hydrazone derivatives

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