Irreversible inhibitors are therefore the equivalent of poisons in heterogeneous catalysis. Safety of 1,1′-Diacetylferrocene, 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. In a patent，Which mentioned a new discovery about 1273-94-5
Four new diferrocenyl hydrazone?enone compounds were obtained through a two-step reaction process involving 1,1?-diacetylferrocene, hydrazides, and ferrocenecarboxaldehyde. The structural characterization of two compounds, 6 and 7, through single-crystal X-ray diffraction showed the presence of a stable eclipsed conformation with the two ferrocenyl moieties oriented in trans geometries. The electrochemical and metal-ion sensing properties of the diferrocenyl-bifunctionalized compounds were explored to understand their potential in electronic communication and as receptor molecules. Compounds 1,1?-[(eta5-C5H5)Fe(eta5-C5H4)CH=CHC(O)(eta5-C5H4)Fe{(eta5-C5H4)C(CH3)=N?N(H)C(O)?R}] [R = C6H4OH (6), C6H4N-p (7)], showed selective interactions with Pb2+cations and distinct binding interactions with bovine serum albumin (BSA) protein. The mode of the metal?receptor interaction was established through DFT studies. The redox properties of the diferrocenyl compounds with variable end groups revealed distinct electronic communication between the two electroactive groups.
If you are interested in 1273-94-5, you can contact me at any time and look forward to more communication. The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules. Safety of 1,1′-Diacetylferrocene
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