{"id":11983,"date":"2023-01-05T03:44:33","date_gmt":"2023-01-04T19:44:33","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11983"},"modified":"2023-01-05T03:44:33","modified_gmt":"2023-01-04T19:44:33","slug":"elguero-jose-et-al-published-their-research-in-bulletin-de-la-societe-chimique-de-france-in-1966-cas-934-48-5","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11983","title":{"rendered":"Elguero, Jose et al. published their research in Bulletin de la Societe Chimique de France in 1966 | CAS: 934-48-5"},"content":{"rendered":"<p>Azoles.  XIV.  Ultraviolet study of pyrazoles was written by Elguero, Jose;Jacquier, Robert;Nguyen Tien Duc Hong Cung. And the article was included in Bulletin de la Societe Chimique de France in 1966.<a href=\"https:\/\/www.ambeed.com\/products\/934-48-5.html\">Synthetic Route of C6H9N3O<\/a> This article mentions the following:<\/p>\n<p>The uv spectra of 170 NH and N-substituted pyrazoles of general structure I were determined at 95\u00b0 in EtOH. Some of the substituents were Me, CONH2, Ac, p-MeC6H4SO2, Ph, p-BrC6H4, p-O2NC6H4, 2,4-(O2N)2C6H3, and 2,4,6-(O2N)3C6H2. In the 2,4-(O2N)2C6H3 and 2,4,6-(O2N)3C6H2 series a time dependence of spectra is noted. Uv spectra are able to identify pairs of N-substituted pyrazole isomers. 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\">Synthetic Route of C6H9N3O<\/a>).<\/p>\n<p>3,5-Dimethyl-1H-pyrazole-1-carboxamide (cas: 934-48-5) belongs to pyrazole derivatives. As is the case with imidazoles, the pyrazole ring offers many opportunities to create new multiring systems that incorporate this heterocycle. 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\/934-48-5.html\">Synthetic Route of C6H9N3O<\/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. As is the case with imidazoles, the pyrazole ring offers many opportunities to create new multiring systems that incorporate this heterocycle. 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\/934-48-5.html\">Synthetic Route of C6H9N3O<\/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-11983","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>Elguero, Jose et al. published their research in Bulletin de la Societe Chimique de France in 1966 | CAS: 934-48-5 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Azoles. XIV. Ultraviolet study of pyrazoles was written by Elguero, Jose;Jacquier, Robert;Nguyen Tien Duc Hong Cung. And the article was included in Bulletin de la Societe Chimique de France in 1966.Synthetic Route of C6H9N3O 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=11983\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Elguero, Jose et al. published their research in Bulletin de la Societe Chimique de France in 1966 | CAS: 934-48-5 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"Azoles. XIV. Ultraviolet study of pyrazoles was written by Elguero, Jose;Jacquier, Robert;Nguyen Tien Duc Hong Cung. 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XIV. Ultraviolet study of pyrazoles was written by Elguero, Jose;Jacquier, Robert;Nguyen Tien Duc Hong Cung. 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