{"id":12024,"date":"2023-01-06T03:43:17","date_gmt":"2023-01-05T19:43:17","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=12024"},"modified":"2023-01-06T03:43:17","modified_gmt":"2023-01-05T19:43:17","slug":"tretyakov-e-v-et-al-published-their-research-in-izvestiya-akademii-nauk-seriya-khimicheskaya-in-1996-cas-54210-32-1","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=12024","title":{"rendered":"Tretyakov, E. V. et al. published their research in Izvestiya Akademii Nauk, Seriya Khimicheskaya in 1996 | CAS: 54210-32-1"},"content":{"rendered":"<p>Synthesis of vicinal aminoiodo- and (acetylamino)iodo-1-alkylpyrazoles was written by Tretyakov, E. V.;Vasilevsky, S. F.. And the article was included in Izvestiya Akademii Nauk, Seriya Khimicheskaya in 1996.<a href=\"https:\/\/www.ambeed.com\/products\/54210-32-1.html\">Safety of 1-Methyl-3-nitro-1H-pyrazole<\/a> This article mentions the following:<\/p>\n<p>One-pot acylation-iodination of 3- and 5-amino-1-alkylpyrazoles gave 3- and 5-acetamido-4-iodo-1-alkylpyrazoles. Reduction of iodonitropyrazoles with SnCl<sub>2<\/sub> in HCl gave 3- and 5-iodo- and 3,5-diiodo-4-amino-1-methylpyrazole. In the experiment, the researchers used many compounds, for example, 1-Methyl-3-nitro-1H-pyrazole (cas: 54210-32-1<a href=\"https:\/\/www.ambeed.com\/products\/54210-32-1.html\">Safety of 1-Methyl-3-nitro-1H-pyrazole<\/a>).<\/p>\n<p>1-Methyl-3-nitro-1H-pyrazole (cas: 54210-32-1) 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 can be selectively lithiated at different carbons and subsequently react with electrophiles depending on the substitution patterns.<a href=\"https:\/\/www.ambeed.com\/products\/54210-32-1.html\">Safety of 1-Methyl-3-nitro-1H-pyrazole<\/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>1-Methyl-3-nitro-1H-pyrazole (cas: 54210-32-1) 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 can be selectively lithiated at different carbons and subsequently react with electrophiles depending on the substitution patterns.<a href=\"https:\/\/www.ambeed.com\/products\/54210-32-1.html\">Safety of 1-Methyl-3-nitro-1H-pyrazole<\/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-12024","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>Tretyakov, E. 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