A new synthetic route of 17524-05-9

Here is just a brief introduction to this compound(17524-05-9)Category: nitriles-buliding-blocks, more information about the compound(Bis(acetylacetonato)dioxomolybdenum(VI)) is in the article, you can click the link below.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Dioxomolybdenum(VI) complexes with 3-methoxy salicylidene-N-alkyl substituted thiosemicarbazones. Synthesis, characterization, enzyme inhibition and antioxidant activity, published in 2019-10-15, which mentions a compound: 17524-05-9, mainly applied to crystal structure oxomolybdenum propylsalicylidene thiosemicarbazone; molybdenum alkylsalicylidene thiosemicarbazone preparation tyrosinase collagenase inhibition antioxidant activity, Category: nitriles-buliding-blocks.

3-Methoxysalicylidene N-alkyl-thiosemicarbazones (L) (alkyl is Pr, Bu, pentyl or hexyl) were synthesized. The reaction of the ONS donor ligands with [MoO2(acac)2] in MeOH yielded the mixed ligand complexes bearing a solvent mol. as co-ligand, [MoO2(L)(MeOH)]. The ligands and complexes were characterized by using anal. and spectroscopic methods. As a representative sample, the dioxomolybdenum(VI) complex of the N4-butyl-substituted thiosemicarbazone was crystallog. examined to ensure the expected structures. X-ray data showed a distorted octahedral environment of Mo center. Tyrosinase, collagenase inhibition and antioxidant properties of the compounds were studied using spectroscopic methods. The ligand and complexes exhibited the different inhibitory activities depending on N-alkyl substituents. Similarly, also the antioxidant capacity of the compounds changed in relation to the substituents.

Here is just a brief introduction to this compound(17524-05-9)Category: nitriles-buliding-blocks, more information about the compound(Bis(acetylacetonato)dioxomolybdenum(VI)) is in the article, you can click the link below.

Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts