Manikandan, Rajendran et al. published their research in Inorganica Chimica Acta in 2014 | CAS: 65-22-5

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Product Details of 65-22-5

Synthesis, structure and in vitro biological activity of pyridoxal N(4)-substituted thiosemicarbazone cobalt(III) complexes was written by Manikandan, Rajendran;Vijayan, Paranthaman;Anitha, Panneerselvam;Prakash, Govindan;Viswanathamurthi, Periasamy;Butcher, Ray Jay;Velmurugan, Krishnaswamy;Nandhakumar, Raju. And the article was included in Inorganica Chimica Acta in 2014.Product Details of 65-22-5 The following contents are mentioned in the article:

Cobalt(III) complexes containing pyridoxal N(4)-substituted thiosemicarbazone ligands with the composition [Co(HL1-2·Cl)(HL1-2·H2O)] (1–2) were synthesized from the reaction of [CoCl2(PPh3)2] and pyridoxal N-methyl-thiosemicarbazone hydrochloride (H3L1·Cl)/pyridoxal N-phenyl-thiosemicarbazone hydrochloride (H3L2·Cl). The richness of the coordination chem. of this ligand is highlighted by the modulation of its charge from neutral (H3L·Cl) (L) to dianionic (HL·Cl) (L2-) and monoanionic forms (HL·H2O) (L–) and coordinated as tridentate bineg. mode around cobalt(III) ion by forming neutral complex. The new complexes were characterized by various anal. and spectroscopic techniques (IR, electronic, 1H NMR and ESI-Mass). The x-ray crystal structure of the complex 2, demonstrated distorted octahedral coordination geometry around the metal center. Further, the study of effect of substitution (CH3 or Ph) on terminal N(4)-nitrogen of thiosemicarbazone exhibited its influence on the potential binding and cleavage ability with DNA, BSA binding, free radical scavenging and cytotoxicity. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Product Details of 65-22-5).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Product Details of 65-22-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts