Synthetic Route of 1271-48-3, Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction by binding to a specific portion of an enzyme and thus slowing or preventing a reaction from occurring. 1271-48-3, Name is 1,1′-Ferrocenedicarboxaldehyde, molecular weight is 242.0516. molecular formula is C12H10FeO2. In an Article，once mentioned of 1271-48-3
The synthesis, electrochemical, electronic, and cation sensing properties of multinuclear nitrogen-rich [2.2]- and [3.3]-mixed ferrocene and ruthenocene metallocenophanes are presented. Structural features of these new structural motifs are that the two redox organometallics fragments are linked by unsaturated nitrogen functionalities, for example, carbodiimide or aldimine, as well as the nitrogen atom is directly attached to the ruthenocene unit. The key bis(iminophosphorane) 3 is readily prepared by the Staudinger reaction between triphenylphosphine and 1,1?-diazidoruthenocene 2, which has been prepared from 1,1?- dilithioruthenocene and 2,4,6-trisopropylbenzenesulfonyl azide (trisyl azide). Subsequent aza-Wittig reactions of 3 with the appropriate carbonyl or thiocarbonyl compounds provided the opened ruthenocenebased isothiocyanate 4, and the closed carbodiimide 5 and aldimines 6 and 7. Spectroelectrochemical studies of carbodiimide 5 and aldimine 7 revealed the presence of low-energy bands in the near-IR region in the partially oxidized forms, at 1029 and 1481 nm, respectively, which indicate the existence of intramolecular charge transfer between the iron and the ruthenium centers. The experimental data and conclusions are supported by DFT computations. Moreover, the aldimine 7 behaves as a selective colorimetric chemosensor molecules for Zn2+ ions. The low-energy (LE) band of the absorption spectrum of this compound is red-shifted by 99 nm, only in the presence of Zn2+ ions. This change in the absorption spectrum is accompanied by a dramatic color change, which allows the potential for “naked eye” detection.
Synthesis of multifunctional aza-substituted ruthenocene derivatives displaying charge-transfer transitions And selective Zn(II) ions sensing properties
The result showed that such a combination of chemo- and biocatalysis improved the catalytic yield more than two times compared with that of sole metal catalysis. We will look forword to the important role of 1271-48-3, and how the biochemistry of the body works.Synthetic Route of 1271-48-3
Reference：
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion