{"id":12003,"date":"2023-01-05T03:46:11","date_gmt":"2023-01-04T19:46:11","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=12003"},"modified":"2023-01-05T03:46:11","modified_gmt":"2023-01-04T19:46:11","slug":"sennitskaya-l-v-et-al-published-their-research-in-khimiya-geterotsiklicheskikh-soedinenii-in-1977-cas-63725-52-0","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=12003","title":{"rendered":"Sennitskaya, L. V. et al. published their research in Khimiya Geterotsiklicheskikh Soedinenii in 1977 | CAS: 63725-52-0"},"content":{"rendered":"<p>IR-spectroscopic study of the structure of indazoles, pyrazolo[3,4-b]pyridines, and pyrazolo[3,4-b]pyrazine was written by Sennitskaya, L. V.;Timoshenkova, Yu. D.;Kikot, B. S.;Pentin, Yu. A.;Blanko, F. F.;Korbukh, I. A.;Preobrazhenskaya, M. N.. And the article was included in Khimiya Geterotsiklicheskikh Soedinenii in 1977.<a href=\"https:\/\/www.ambeed.com\/products\/63725-52-0.html\">Product Details of 63725-52-0<\/a> This article mentions the following:<\/p>\n<p>The IR of I (R = H, Me), II, III (R = H, NH2, Me2N), IV, V (R, R1 = H, Me), and VI were discussed. A band at 2500-3300 cm-1, shifted to 2000-2400 cm-1 by deuteration, indicated that intermol. H bonding occurred in the crystals of the NH compounds The IR also indicated that protonation of III (R = NH2) occurred on one of the ring N atoms. In the experiment, the researchers used many compounds, for example, 6-Chloro-1-methylpyrazolo[5,4-b]pyridine (cas: 63725-52-0<a href=\"https:\/\/www.ambeed.com\/products\/63725-52-0.html\">Product Details of 63725-52-0<\/a>).<\/p>\n<p>6-Chloro-1-methylpyrazolo[5,4-b]pyridine (cas: 63725-52-0) belongs to pyrazole derivatives. The 1H-pyrazole provides an excellent means by which to provide the requisite hydrogen bond acceptor\u2013donor 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\/63725-52-0.html\">Product Details of 63725-52-0<\/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>6-Chloro-1-methylpyrazolo[5,4-b]pyridine (cas: 63725-52-0) belongs to pyrazole derivatives. The 1H-pyrazole provides an excellent means by which to provide the requisite hydrogen bond acceptor\u2013donor 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\/63725-52-0.html\">Product Details of 63725-52-0<\/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-12003","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>Sennitskaya, L. 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And the article was included in Khimiya Geterotsiklicheskikh Soedinenii in 1977.Product Details of 63725-52-0 This article mentions the following:","og_url":"https:\/\/www.pyrazoles-derivatives.com\/?p=12003","og_site_name":"pyrazoles-derivatives","article_published_time":"2023-01-04T19:46:11+00:00","author":"Jessica.F","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Jessica.F","Est. reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=12003","url":"https:\/\/www.pyrazoles-derivatives.com\/?p=12003","name":"Sennitskaya, L. 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