2746-61-4 Usage
Hydrazine derivative
A compound that contains a hydrazine functional group (-NH-NH2) and has undergone chemical modification to form a new compound.
Pyridine ring
A six-membered aromatic ring with one nitrogen atom, which is present in 2-[2-(2-chlorobenzylidene)hydrazinyl]pyridine.
Schiff bases and hydrazones formation
The ability of 2-[2-(2-chlorobenzylidene)hydrazinyl]pyridine to react with aldehydes and ketones to form Schiff bases and with aldehydes to form hydrazones, which are important intermediates in organic synthesis.
Biological activities
The potential of 2-[2-(2-chlorobenzylidene)hydrazinyl]pyridine to exhibit antimicrobial and anticancer properties, which have been studied in various research.
Ligand in coordination chemistry
The ability of 2-[2-(2-chlorobenzylidene)hydrazinyl]pyridine to form complexes with metal ions, which is important in the study of coordination compounds and their properties.
Check Digit Verification of cas no
The CAS Registry Mumber 2746-61-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2746-61:
(6*2)+(5*7)+(4*4)+(3*6)+(2*6)+(1*1)=94
94 % 10 = 4
So 2746-61-4 is a valid CAS Registry Number.
2746-61-4Relevant articles and documents
Synthesis, characterization, structural-activity relationship and biomolecular interaction studies of heteroleptic Pd(II) complexes with acetyl pyridine scaffold
Bhatt, Bhupesh S.,Pandya, Juhi,Patel, Mohan N.,Patel, Nikita J.,Pathak, Chandramani,Vaidya, Foram U.,Vekariya, Pankajkumar A.
, (2020/07/14)
A series of substituted hydrazinyl pyridine based Schiff base ligands (L1–L6) and corresponding palladium(II) complexes were synthesized and characterized by conductivity measurement, 1H NMR, 13C NMR and liquid
Efficient synthesis of 3-substituted 1,2,4-triazolo[4,3-a]pyridine by [bis(trifluroacetoxy)iodo]benzene-catalyzed oxidative intramolecular cyclization of heterocyclic hydrazones
Padalkar, Vikas S.,Patil, Vikas S.,Phatangare, Kiran R.,Umape, Prashant G.,Sekar
, p. 925 - 938 (2011/04/22)
A series of 1,2,4-triazolopyridines have been prepared by oxidative intramolecular cyclization of heterocyclic hydrazones with [bis(trifluroacetoxy) iodo]benzene. General applicability of this simple transformation was confirmed by synthesis of 1,2,4-triazolo[4,3-a]pyridine. The advantages of this protocol are the nontoxicity of catalyst and shorter reaction time to obtain good preparative yield.