{"id":12284,"date":"2023-01-25T04:21:32","date_gmt":"2023-01-24T20:21:32","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=12284"},"modified":"2024-10-21T19:08:55","modified_gmt":"2024-10-21T11:08:55","slug":"safronova-l-a-et-al-published-their-research-in-koordinatsionnaya-khimiya-in-1987-cas-934-48-5","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=12284","title":{"rendered":"Safronova, L. A. et al. published their research in Koordinatsionnaya Khimiya in 1987 | CAS: 934-48-5"},"content":{"rendered":"<p>Preparation and structure of cobalt(II) complexes with 3,5-dimethylpyrazole was written by Safronova, L. A.;Komyagin, N. T.;Yanovskii, A. I.;Struchkov, Yu. T.;Shebaldova, A. D.. And the article was included in Koordinatsionnaya Khimiya in 1987.<a href=\"https:\/\/www.ambeed.com\/products\/934-48-5.html\">Reference of 934-48-5<\/a> This article mentions the following:<\/p>\n<p>CoCl<sub>2<\/sub> reacted with 3,5-dimethylpyrazolylcarbamide in iso-PrOH with heating to give CoL<sub>2<\/sub>Cl<sub>2<\/sub> (L = 3,5-dimethylpyrazole). CoL<sub>2<\/sub>Cl<sub>2<\/sub> is monoclinic, space group <em>C<\/em>2\/<em>c<\/em>, with <em>a<\/em> 15.011(1), <em>b<\/em> 8.2732(6), <em>c<\/em> 24.053(2) \u9474? \u704f?96.045(7)\u93ba? <em>Z<\/em> = 8, <em>R<\/em> = 0.041, <em>R<\/em><sub>w<\/sub> = 0.054. CoL<sub>2<\/sub>Cl<sub>2<\/sub> has a distorted tetrahedral structure in which L is monodentate. CoL<sub>2<\/sub>Cl<sub>2<\/sub> was also characterized by IR and <sup>13<\/sup>C NMR spectra. In the experiment, the researchers used many compounds, for example, 3,5-Dimethyl-1H-pyrazole-1-carboxamide (cas: 934-48-5<a href=\"https:\/\/www.ambeed.com\/products\/934-48-5.html\">Reference of 934-48-5<\/a>).<\/p>\n<p>3,5-Dimethyl-1H-pyrazole-1-carboxamide (cas: 934-48-5) belongs to pyrazole derivatives. The 1H-pyrazole provides an excellent means by which to provide the requisite hydrogen bond acceptor\u95b3\u30e6\u5f86onor motifs, whether as a monocyclic ring or as a fused indazole ring. Pyrazole rings have been used as core components of several leading non-steroidal anti-inflammatory drugs (NSAIDs) and antihypertensive drugs. It has also been found to be useful as a bifunctional ligand for metal catalysis.<a href=\"https:\/\/www.ambeed.com\/products\/934-48-5.html\">Reference of 934-48-5<\/a><\/p>\n<p>Referemce:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">Pyrazole &#8211; Wikipedia<\/a>,<br \/><a href=\"https:\/\/www.sciencedirect.com\/topics\/chemistry\/pyrazoles\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>3,5-Dimethyl-1H-pyrazole-1-carboxamide (cas: 934-48-5) belongs to pyrazole derivatives. The 1H-pyrazole provides an excellent means by which to provide the requisite hydrogen bond acceptor\u95b3\u30e6\u5f86onor motifs, whether as a monocyclic ring or as a fused indazole ring. Pyrazole rings have been used as core components of several leading non-steroidal anti-inflammatory drugs (NSAIDs) and antihypertensive drugs. It has also been found to be useful as a bifunctional ligand for metal catalysis.<a href=\"https:\/\/www.ambeed.com\/products\/934-48-5.html\">Reference of 934-48-5<\/a><\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[829,131],"tags":[128],"class_list":["post-12284","post","type-post","status-publish","format-standard","hentry","category-934-48-5","category-pyrazoles-derivatives","tag-100-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Safronova, L. A. et al. published their research in Koordinatsionnaya Khimiya in 1987 | CAS: 934-48-5 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Preparation and structure of cobalt(II) complexes with 3,5-dimethylpyrazole was written by Safronova, L. A.;Komyagin, N. T.;Yanovskii, A. 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