{"id":12074,"date":"2023-01-30T07:02:31","date_gmt":"2023-01-29T23:02:31","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=12074"},"modified":"2023-01-30T07:02:31","modified_gmt":"2023-01-29T23:02:31","slug":"hennig-horst-et-al-published-their-research-in-zeitschrift-fuer-chemie-in-1971-cas-19959-77-4","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=12074","title":{"rendered":"Hennig, Horst et al. published their research in Zeitschrift fuer Chemie in 1971 | CAS: 19959-77-4"},"content":{"rendered":"<p>Coordination tendencies of acidic amino groups.  VIII.  Complexing behavior of 3-methyl-5-pyridyl-2-pyrazole was written by Hennig, Horst;Daute, Ingeborg. And the article was included in Zeitschrift fuer Chemie in 1971.<a href=\"https:\/\/www.ambeed.com\/products\/19959-77-4.html\">Application of 19959-77-4<\/a> This article mentions the following:<\/p>\n<p>3-Methyl-5-(2-pyridyl)pyrazole (HMPP) reacted with metal acetylacetonates to give the following complexes: [Cu(MPP)2], [Ni(MPP)2], [Co(MPP)3], [Zn(MPP)2], [Pd(MPP)2], (Cu(HMPP)Cl2] and [Co(HMPP)Cl2]. In the experiment, the researchers used many compounds, for example, 2-(5-Methyl-1H-pyrazol-3-yl)pyridine (cas: 19959-77-4<a href=\"https:\/\/www.ambeed.com\/products\/19959-77-4.html\">Application of 19959-77-4<\/a>).<\/p>\n<p>2-(5-Methyl-1H-pyrazol-3-yl)pyridine (cas: 19959-77-4) belongs to pyrazole derivatives. An alternative way to synthesize multisubstituted pyrazoles is the Csingle bondH arylation of simple pyrazoles. Pyrazoles are commonly used scaffold molecules in drug discovery projects. The use of pyrazole derivatives is based on their analgesic, anti-inflammatory, antipyretic, antiarrhythmic, sedative, muscle relaxant, neuroleptic, anticonvulsant, monoamine oxidase inhibitory, antidiabetic and antibacterial activities.<a href=\"https:\/\/www.ambeed.com\/products\/19959-77-4.html\">Application of 19959-77-4<\/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>2-(5-Methyl-1H-pyrazol-3-yl)pyridine (cas: 19959-77-4) belongs to pyrazole derivatives. An alternative way to synthesize multisubstituted pyrazoles is the Csingle bondH arylation of simple pyrazoles. Pyrazoles are commonly used scaffold molecules in drug discovery projects. The use of pyrazole derivatives is based on their analgesic, anti-inflammatory, antipyretic, antiarrhythmic, sedative, muscle relaxant, neuroleptic, anticonvulsant, monoamine oxidase inhibitory, antidiabetic and antibacterial activities.<a href=\"https:\/\/www.ambeed.com\/products\/19959-77-4.html\">Application of 19959-77-4<\/a><\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[131],"tags":[128],"class_list":["post-12074","post","type-post","status-publish","format-standard","hentry","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>Hennig, Horst et al. published their research in Zeitschrift fuer Chemie in 1971 | CAS: 19959-77-4 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Coordination tendencies of acidic amino groups. VIII. Complexing behavior of 3-methyl-5-pyridyl-2-pyrazole was written by Hennig, Horst;Daute, Ingeborg. And the article was included in Zeitschrift fuer Chemie in 1971.Application of 19959-77-4 This article mentions the following:\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.pyrazoles-derivatives.com\/?p=12074\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Hennig, Horst et al. published their research in Zeitschrift fuer Chemie in 1971 | CAS: 19959-77-4 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"Coordination tendencies of acidic amino groups. VIII. Complexing behavior of 3-methyl-5-pyridyl-2-pyrazole was written by Hennig, Horst;Daute, Ingeborg. 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