A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Application In Synthesis of 1-(2-Hydroxyethyl)piperidine, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 3040-44-6, Name is 1-(2-Hydroxyethyl)piperidine, molecular formula is C7H15NO. In a Article, authors is Arsenyan, Pavel，once mentioned of 3040-44-6
Synthetic protocols for the preparation of selenium analogues of raloxifene were elaborated. General aim of the current research is to improve the positive impact of selenium atom introduction in drug design. Antiproliferative activity on CCL-8 (mouse sarcoma), MDA-MB-435s (human melanoma), MES-SA (human uterus sarcoma), MCF-7 (human breast adenocarcinoma), HT-1080 (human fibrosarcoma), MG-22A (mouse hepatoma) tumor cell lines, and normal cell line NIH 3T3 (mouse fibroblasts) was studied. Influence of aminoethoxy “tail” and benzoyl group position on SAR was discussed. Results of in vivo studies on BALB/c female mice with 4T1 cell induced breast cancer model showed that selenium analogue of raloxifene is able to suppress estrogen-depending tumor growth.
Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about is helpful to your research. Application In Synthesis of 1-(2-Hydroxyethyl)piperidine
Reference：
Piperidine – Wikipedia,
Piperidine | C5H5271N – PubChem