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4-(2-chlorophenylimino)methyl-5-(hydroxymethyl)-2-methylpyridin-3-ol is a complex organic compound with the molecular formula C15H13ClN2O2. It is characterized by a pyridin-3-ol core, which is a derivative of pyridine with a hydroxyl group at the 3-position. The molecule features a 2-methyl group attached to the pyridine ring, and a 4-(2-chlorophenylimino)methyl group, which is a 2-chlorophenyl imine connected to the pyridine through a methylene bridge. Additionally, it has a 5-(hydroxymethyl) group, which is a hydroxymethyl moiety attached at the 5-position of the pyridine ring. 4-(2-chlorophenylimino)methyl-5-(hydroxymethyl)-2-methylpyridin-3-ol is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of pharmaceuticals or other complex molecules, due to its diverse functional groups and structural features.

4943-91-3

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4943-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4943-91-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4943-91:
(6*4)+(5*9)+(4*4)+(3*3)+(2*9)+(1*1)=113
113 % 10 = 3
So 4943-91-3 is a valid CAS Registry Number.

4943-91-3Downstream Products

4943-91-3Relevant academic research and scientific papers

Pyridoxal derivatized copper(II) complexes: Evaluation of antioxidant, catecholase, and DNA cleavage activity

Pereira, Mateus Brum,Fontana, Liniquer Andre,Siqueira, Josiéli Demetrio,Auras, Bruna L.,da Silva, Marcos P.,Neves, Ademir,Gabriel, Philipe,Terenzi, Hernán,Iglesias, Bernardo Almeida,Back, Davi Fernando

, p. 561 - 575 (2018)

This manuscript describes the synthesis, characterization and structural analysis of copper(II) complexes with pyridoxal-type bidentate ligands, obtained from the condensation between pyridoxal and ortho-halogenated substituted anilines (C1–C5). The complexes C1, C2 and C5 were measured by X-ray single crystal analysis which showed classic and trifurcated hydrogen bonds and interaction as a sigma-hole between the oxygen atoms of the iodine ligand derivative in the complex C5. All compounds were tested as mimetics of superoxide dismutase (SOD), through NBT photoreduction method in aqueous solution of pH 7.8, but the complex C5 showed an expressive IC50 of 0.4 μM. In addition, catecholase-like activity of C1–C5 in the presence of the substrate 3,5-di-tert-butylcatechol and cleavage of plasmid DNA were also evaluated. Again, the best results were associated with the complex C5 containing iodine in the ortho position.

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