Brief introduction of 1273-94-5

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. name: 1,1′-Diacetylferrocene

Irreversible inhibitors are therefore the equivalent of poisons in heterogeneous catalysis. name: 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

New azaalkyl or azacrown ferrocenyl compounds containing a C5H4COCC- linkage are accessible from mono- or diacetylferrocene upon treatment with the appropriate aldehydes (CHOC6H4-p-R, R = NEt2, N-aza-15-crown-5). Preliminary results concerning the electrochemical behaviour of complexes [(C5H5)Fe(C5H4COCH=CHC6H4NEt2)] (3a), [Fe(C5H4COCH=CHC6H4NEt2)2] (5a), the novel ferrocenophane [Fe(C5H4COCH2)2CHC6H4NEt2] (6a) and its protonated species [Fe(C5H4COCH2)2CHC6H4NHEt2][BF4] (7a), are reported. The ferrocenyl ligand 5a is a rare example of a molecule which is both electroactive and fluorescent.

Mono- and 1,1′-disubstituted aza ferrocenyl compounds: Evidence for an original electroactive fluorescent species

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. name: 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