{"id":5617,"date":"2021-07-30T06:06:27","date_gmt":"2021-07-29T22:06:27","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=5617"},"modified":"2021-07-30T06:06:27","modified_gmt":"2021-07-29T22:06:27","slug":"discovery-of-3112-31-0","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=5617","title":{"rendered":"Discovery of  3112-31-0"},"content":{"rendered":"<p>Adding a certain compound to certain chemical reactions, such as: 3112-31-0, name is 1H-Pyrazole-3,5-dicarboxylic acid, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound  3112-31-0, <a href=\"https:\/\/www.ambeed.com\/products\/3112-31-0.html\">name: 1H-Pyrazole-3,5-dicarboxylic acid<\/a><\/p>\n<p>The mixture solution of Cu(NO3)2*3H2O (0.2 mmol, 48 mg), 4,4&#8242;-bipyridine (0.2 mmol, 31 mg) and pyrazole-3,5-dicarboxylic acid(0.2 mmol, 35 mg) in the deionized water (7 mL), DMF (2 mL)and ethanol (3 mL) was sealed in a 20 mL glass vial. Then, the mixturewas heated at 120\u00b0 C for 1 day and then slowly cooled down toroom temperature. The blue crystals of 3 were obtained. Yield:10 mg (16percent) based on copper salt Anal. Calcd for Cu5C50H46N14O24:C, 38.88; H, 3.00; N, 12.69. Found: C, 38.79; H, 2.85; N, 13.00percent. FTIRpeaks (KBr, cm-1): 3368br (m(OH)), 1646s (mas(OCO)), 1599s (m(CN)), 1533w, 1481w, 1407w, 1387m (ms(OCO)), 1288s, 1224m,1065w, 1020w, 817w, 806w, 778 m. UV-vis (diffuse reflectance,cm-1): 14407.<\/p>\n<p>If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.<\/p>\n<p>Reference:<br \/><a href=\"https:\/\/doi.org\/10.1016\/j.poly.2017.01.015\">Article; Klongdee, Fatima; Boonmak, Jaursup; Moubaraki, Boujemaa; Murray, Keith S.; Youngme, Sujittra; Polyhedron; vol. 126; (2017); p. 8 &#8211; 16;<\/a>,<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<\/p>\n","protected":false},"excerpt":{"rendered":"<p>If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[140,131],"tags":[126],"class_list":["post-5617","post","type-post","status-publish","format-standard","hentry","category-3112-31-0","category-pyrazoles-derivatives","tag-m-w100-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Discovery of<\/title>\n<meta name=\"description\" content=\"Adding a certain compound to certain chemical reactions, such as: 3112-31-0, name is 1H-Pyrazole-3,5-dicarboxylic acid, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. 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