{"id":9584,"date":"2022-04-11T04:48:22","date_gmt":"2022-04-10T20:48:22","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=9584"},"modified":"2022-04-11T04:48:22","modified_gmt":"2022-04-10T20:48:22","slug":"some-scientific-research-about-1300746-79-5","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=9584","title":{"rendered":"Some scientific research about 1300746-79-5"},"content":{"rendered":"<p>Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 1300746-79-5, is researched, SMILESS is F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F, Molecular C13H8CuF3N2Journal, Article, Beilstein Journal of Organic Chemistry called Comparative profiling of well-defined copper reagents and precursors for the trifluoromethylation of aryl iodides, Author is Kaplan, Peter T.; Lloyd, Jessica A.; Chin, Mason T.; Vicic, David A., the main research direction is aryltrifluoromethyl preparation; aryl iodide copper reagent trifluoromethylation; benchmarking; copper; fluorine; fluoroalkylation; trifluoromethylation.<a href=\"https:\/\/www.ambeed.com\/products\/1300746-79-5.html\">Name: (1,10-Phenanthroline)(trifluoromethyl)copper(I)<\/a>.<\/p>\n<p>A number of copper reagents e.g., I were compared for their effectiveness in trifluoromethylating 4-iodobiphenyl, 4-iodotoluene, and 2-iodotoluene. Yields over time were plotted in order to refine our understanding of each reagent performance, identify any bottlenecks, and provide more insight into the rates of the reactions. Interestingly, differences in reactivity were observed when a well defined [LCuCF3] complex I was employed directly or generated in situ from precursors by published reports. Relative reactivities were also found to highly dependent on the nature of the iodoarenes.<\/p>\n<p>There are many compounds similar to this compound(1300746-79-5)<a href=\"https:\/\/www.ambeed.com\/products\/1300746-79-5.html\">Name: (1,10-Phenanthroline)(trifluoromethyl)copper(I)<\/a>. if you want to know more, you can check out my other articles. I hope it will help you\uff0cmaybe you&#8217;ll find some useful information.<\/p>\n<p>Reference:<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>There are many compounds similar to this compound(1300746-79-5)<a href=\"https:\/\/www.ambeed.com\/products\/1300746-79-5.html\">Name: (1,10-Phenanthroline)(trifluoromethyl)copper(I)<\/a>. if you want to know more, you can check out my other articles. I hope it will help you\uff0cmaybe you&#8217;ll find some useful information.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[726,131],"tags":[167],"class_list":["post-9584","post","type-post","status-publish","format-standard","hentry","category-1300746-79-5","category-pyrazoles-derivatives","tag-m-w300-400"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Some scientific research about 1300746-79-5 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 1300746-79-5, is researched, SMILESS is F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F, Molecular C13H8CuF3N2Journal, Article, Beilstein Journal of Organic Chemistry called Comparative profiling of well-defined copper reagents and precursors for the trifluoromethylation of aryl iodides, Author is Kaplan, Peter T.; Lloyd, Jessica A.; Chin, Mason T.; Vicic, David A., the main research direction is aryltrifluoromethyl preparation; aryl iodide copper reagent trifluoromethylation; benchmarking; copper; fluorine; fluoroalkylation; trifluoromethylation.Name: (1,10-Phenanthroline)(trifluoromethyl)copper(I).\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.pyrazoles-derivatives.com\/?p=9584\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Some scientific research about 1300746-79-5 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 1300746-79-5, is researched, SMILESS is F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F, Molecular C13H8CuF3N2Journal, Article, Beilstein Journal of Organic Chemistry called Comparative profiling of well-defined copper reagents and precursors for the trifluoromethylation of aryl iodides, Author is Kaplan, Peter T.; Lloyd, Jessica A.; Chin, Mason T.; Vicic, David A., the main research direction is aryltrifluoromethyl preparation; aryl iodide copper reagent trifluoromethylation; benchmarking; copper; fluorine; fluoroalkylation; trifluoromethylation.Name: (1,10-Phenanthroline)(trifluoromethyl)copper(I).\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.pyrazoles-derivatives.com\/?p=9584\" \/>\n<meta property=\"og:site_name\" content=\"pyrazoles-derivatives\" \/>\n<meta property=\"article:published_time\" content=\"2022-04-10T20:48:22+00:00\" \/>\n<meta name=\"author\" content=\"Jessica.F\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Jessica.F\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9584\",\"url\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9584\",\"name\":\"Some scientific research about 1300746-79-5 | pyrazoles-derivatives\",\"isPartOf\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#website\"},\"datePublished\":\"2022-04-10T20:48:22+00:00\",\"author\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\"},\"description\":\"Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 1300746-79-5, is researched, SMILESS is F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F, Molecular C13H8CuF3N2Journal, Article, Beilstein Journal of Organic Chemistry called Comparative profiling of well-defined copper reagents and precursors for the trifluoromethylation of aryl iodides, Author is Kaplan, Peter T.; Lloyd, Jessica A.; Chin, Mason T.; Vicic, David A., the main research direction is aryltrifluoromethyl preparation; aryl iodide copper reagent trifluoromethylation; benchmarking; copper; fluorine; fluoroalkylation; trifluoromethylation.Name: (1,10-Phenanthroline)(trifluoromethyl)copper(I).\",\"breadcrumb\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9584#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.pyrazoles-derivatives.com\/?p=9584\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9584#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"\u9996\u9875\",\"item\":\"https:\/\/www.pyrazoles-derivatives.com\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Some scientific research about 1300746-79-5\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#website\",\"url\":\"https:\/\/www.pyrazoles-derivatives.com\/\",\"name\":\"pyrazoles-derivatives\",\"description\":\"Several pyrazole derivatives possess important pharmacological activities and they have been proved useful materials in drug research. Pyrazole derivatives play an important role in antitumor agents.\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.pyrazoles-derivatives.com\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\",\"name\":\"Jessica.F\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/en.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/en.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"caption\":\"Jessica.F\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Some scientific research about 1300746-79-5 | pyrazoles-derivatives","description":"Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. 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