{"id":11869,"date":"2022-12-30T07:41:31","date_gmt":"2022-12-29T23:41:31","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11869"},"modified":"2022-12-30T07:41:31","modified_gmt":"2022-12-29T23:41:31","slug":"pundir-s-et-al-published-their-research-in-indian-journal-of-heterocyclic-chemistry-in-2017-cas-15953-73-8","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11869","title":{"rendered":"Pundir, S. et al. published their research in Indian Journal of Heterocyclic Chemistry in 2017 | CAS: 15953-73-8"},"content":{"rendered":"<p>Synthesis and characterization of some symmetrical substituted 1-(2-chloroethyl)pyrazole-based chalcogenides was written by Pundir, S.;Mehta, S. K.;Mobin, S. M.;Bhasin, K. K.. And the article was included in Indian Journal of Heterocyclic Chemistry in 2017.<a href=\"https:\/\/www.ambeed.com\/products\/15953-73-8.html\">Application In Synthesis of 4-Chloro-3,5-dimethyl-1H-pyrazole<\/a> This article mentions the following:<\/p>\n<p>The synthesis of some sym. substituted 1-(2-chloroethyl) pyrazole-based dichalcogenides <strong>I<\/strong> [X = H, Cl, Br, CHO; R = S, Se, Te] and monochalcogenides <strong>II<\/strong> [X = H, Cl] by reacting different 3,4,5-trisubstituted 1-(2-chloroethyl) pyrazole derivatives with in situ prepared Na<sub>2<\/sub>E<sub>2<\/sub> (E = S, Se, Te) and sodium hydrogen selenide, resp. X-ray crystal structure determination of 1,2-bis (2-(4-bromo-3,5-dimethyl-1H-pyrazol-1-yl)ethyl)diselane <strong>I<\/strong> [X = Br; R = Se] revealed intermol. Se\u00b7N\u00b7H interactions between two mols. In the experiment, the researchers used many compounds, for example, 4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8<a href=\"https:\/\/www.ambeed.com\/products\/15953-73-8.html\">Application In Synthesis of 4-Chloro-3,5-dimethyl-1H-pyrazole<\/a>).<\/p>\n<p>4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8) 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\/15953-73-8.html\">Application In Synthesis of 4-Chloro-3,5-dimethyl-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>4-Chloro-3,5-dimethyl-1H-pyrazole (cas: 15953-73-8) 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\/15953-73-8.html\">Application In Synthesis of 4-Chloro-3,5-dimethyl-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-11869","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>Pundir, S. et al. published their research in Indian Journal of Heterocyclic Chemistry in 2017 | CAS: 15953-73-8 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Synthesis and characterization of some symmetrical substituted 1-(2-chloroethyl)pyrazole-based chalcogenides was written by Pundir, S.;Mehta, S. 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