{"id":3704,"date":"2021-04-28T07:50:31","date_gmt":"2021-04-27T23:50:31","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=3704"},"modified":"2021-04-28T07:50:31","modified_gmt":"2021-04-27T23:50:31","slug":"simple-exploration-of-5-amino-1-4-chlorophenyl-1h-pyrazole-4-carbonitrile","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=3704","title":{"rendered":"Simple exploration of 5-Amino-1-(4-chlorophenyl)-1H-pyrazole-4-carbonitrile"},"content":{"rendered":"<p>In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 51516-67-7 as follows. <a href=\"https:\/\/www.ambeed.com\/products\/51516-67-7.html\">Recommanded Product: 5-Amino-1-(4-chlorophenyl)-1H-pyrazole-4-carbonitrile<\/a><\/p>\n<p>General procedure: The experimental procedure was similar to synthesis of analogs1(aei). 5-amino-1-aryl-1H-pyrazole-4-carbonitriles 4(aei)(0.001 mol) were reacted with 2.0 mL of 1,3-diaminopropane andcarbon disulfide (0.004 mol). The temperaturewas 85-95oC and thereaction time was 14-16 hours. The reaction mixture was pouredinto cold water, the precipitate was filtered out and washed withcold water. The reactions were accompanied by means of TLC anddichloromethane as eluent.<\/p>\n<p>According to the analysis of related databases, 51516-67-7, the application of this compound in the production field has become more and more popular.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>According to the analysis of related databases, 51516-67-7, the application of this compound in the production field has become more and more popular.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[232,131],"tags":[127],"class_list":["post-3704","post","type-post","status-publish","format-standard","hentry","category-51516-67-7","category-pyrazoles-derivatives","tag-m-w200-300"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Simple exploration of 5-Amino-1-(4-chlorophenyl)-1H-pyrazole-4-carbonitrile<\/title>\n<meta name=\"description\" content=\"In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. 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An updated downstream synthesis route of 51516-67-7 as follows. Recommanded Product: 5-Amino-1-(4-chlorophenyl)-1H-pyrazole-4-carbonitrile","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.pyrazoles-derivatives.com\/?p=3704","og_locale":"en_US","og_type":"article","og_title":"Simple exploration of 5-Amino-1-(4-chlorophenyl)-1H-pyrazole-4-carbonitrile","og_description":"In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 51516-67-7 as follows. 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