Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 211915-84-3, Name is Ethyl 3-(2-(((4-cyanophenyl)amino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate, molecular formula is C27H26N6O3, belongs to pyridine-derivatives compound. In a document, author is Song, Li-Cheng, introduce the new discover, HPLC of Formula: C27H26N6O3.
A Biomimetic Model for the Active Site of [Fe]-H(2)ase Featuring a 2-Methoxy-3,5-dimethyl-4-phosphato-6-acylmethylpyridine Ligand
Herein, we report the first 3,5-dimethyl-4-phosphatopyridine moiety containing [Fe]-H(2)ase model, [2-MeO-3,5-Me-2-4-OP-O(OPh)(2)-6-COCH2C5N]Fe(CO)(2)(eta(2)-6-Me-2-SC5H3N) (7), prepared by a multistep synthetic method including seven separate reaction steps. The first three reaction steps are utilized to prepare the organic precursors 4-TBSO-3,5,6-trimethyl-2-pyridone (1), 2-methoxy-4-TBSO-3,5,6-trimethylpyridine (2), and 2-methoxy-4-TBSO-3,5-dimethyl-6-chloromethylpyridine (3). The next three reaction steps are used to prepare the organometallic precursors (2-MeO-4-TBSO-3,5-Me-2-6-COCH2C5N)Fe(CO)(3)I (4), (2-MeO-4-TBSO-3,5-Me-2-6-COCH2C5N)Fe(CO)(2)(eta(2)-6-Me-2-SC5H3N) (5), and (2-MeO-4-HO-3,5-Me-2-6-COCH2C5N)Fe(CO)2(eta(2)-6-Me-2-SC5H3N) (6). The final step is employed to prepare target model 7 by an esterification reaction of 6 with O=P(OPh)(2)Cl in the presence of Et3N. All of the prepared organic and organometallic compounds are new and have been characterized by elemental analysis and spectroscopy and, for some of them, by X-ray crystallography.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 211915-84-3. HPLC of Formula: C27H26N6O3.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem