{"id":9465,"date":"2022-04-01T11:50:48","date_gmt":"2022-04-01T03:50:48","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=9465"},"modified":"2022-04-01T11:50:48","modified_gmt":"2022-04-01T03:50:48","slug":"the-effect-of-the-change-of-synthetic-route-on-the-product-1300746-79-5","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=9465","title":{"rendered":"The effect of the change of synthetic route on the product 1300746-79-5"},"content":{"rendered":"<p>The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: (1,10-Phenanthroline)(trifluoromethyl)copper(I)(SMILESS: F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F,cas:1300746-79-5) is researched.<a href=\"https:\/\/www.ambeed.com\/products\/1300746-79-5.html\">Name: Tris(triphenylphosphine)chlororhodium<\/a>. The article \u300aRegioselective \u03b2-Trifluoromethylation of \u03b2-Silylporphyrins by Using a Trifluoromethyl Copper Complex\u300b in relation to this compound, is published in European Journal of Organic Chemistry. Let&#8217;s take a look at the latest research on this compound (cas:1300746-79-5).<\/p>\n<p>The authors developed a method for the regioselective \u03b2-trifluoromethylation of \u03b2-silylated Zn(II) porphyrins by using a phenanthroline and triphenylphosphine-ligated trifluoromethyl-copper complex [(phen)(Ph3P)CuCF3]. The regioselective porphyrin trifluoromethylation, which occurs under mild conditions, exhibits excellent substrate generality and functional group compatibility.<\/p>\n<p>From this literature\u300aRegioselective \u03b2-Trifluoromethylation of \u03b2-Silylporphyrins by Using a Trifluoromethyl Copper Complex\u300b,we know some information about this compound(1300746-79-5)<a href=\"https:\/\/www.ambeed.com\/products\/1300746-79-5.html\">SDS of cas: 1300746-79-5<\/a>, but this is not all information, there are many literatures related to this compound(1300746-79-5).<\/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>From this literature\u300aRegioselective \u03b2-Trifluoromethylation of \u03b2-Silylporphyrins by Using a Trifluoromethyl Copper Complex\u300b,we know some information about this compound(1300746-79-5)<a href=\"https:\/\/www.ambeed.com\/products\/1300746-79-5.html\">SDS of cas: 1300746-79-5<\/a>, but this is not all information, there are many literatures related to this compound(1300746-79-5).<\/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-9465","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>The effect of the change of synthetic route on the product 1300746-79-5 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: (1,10-Phenanthroline)(trifluoromethyl)copper(I)(SMILESS: F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F,cas:1300746-79-5) is researched.Name: Tris(triphenylphosphine)chlororhodium. The article \u300aRegioselective \u03b2-Trifluoromethylation of \u03b2-Silylporphyrins by Using a Trifluoromethyl Copper Complex\u300b in relation to this compound, is published in European Journal of Organic Chemistry. Let&#039;s take a look at the latest research on this compound (cas:1300746-79-5).\" \/>\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=9465\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"The effect of the change of synthetic route on the product 1300746-79-5 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: (1,10-Phenanthroline)(trifluoromethyl)copper(I)(SMILESS: F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F,cas:1300746-79-5) is researched.Name: Tris(triphenylphosphine)chlororhodium. The article \u300aRegioselective \u03b2-Trifluoromethylation of \u03b2-Silylporphyrins by Using a Trifluoromethyl Copper Complex\u300b in relation to this compound, is published in European Journal of Organic Chemistry. Let&#039;s take a look at the latest research on this compound (cas:1300746-79-5).\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.pyrazoles-derivatives.com\/?p=9465\" \/>\n<meta property=\"og:site_name\" content=\"pyrazoles-derivatives\" \/>\n<meta property=\"article:published_time\" content=\"2022-04-01T03:50:48+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=9465\",\"url\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9465\",\"name\":\"The effect of the change of synthetic route on the product 1300746-79-5 | pyrazoles-derivatives\",\"isPartOf\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#website\"},\"datePublished\":\"2022-04-01T03:50:48+00:00\",\"author\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\"},\"description\":\"The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: (1,10-Phenanthroline)(trifluoromethyl)copper(I)(SMILESS: F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F,cas:1300746-79-5) is researched.Name: Tris(triphenylphosphine)chlororhodium. The article \u300aRegioselective \u03b2-Trifluoromethylation of \u03b2-Silylporphyrins by Using a Trifluoromethyl Copper Complex\u300b in relation to this compound, is published in European Journal of Organic Chemistry. Let's take a look at the latest research on this compound (cas:1300746-79-5).\",\"breadcrumb\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9465#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.pyrazoles-derivatives.com\/?p=9465\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9465#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"\u9996\u9875\",\"item\":\"https:\/\/www.pyrazoles-derivatives.com\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"The effect of the change of synthetic route on the product 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":"The effect of the change of synthetic route on the product 1300746-79-5 | pyrazoles-derivatives","description":"The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: (1,10-Phenanthroline)(trifluoromethyl)copper(I)(SMILESS: F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F,cas:1300746-79-5) is researched.Name: Tris(triphenylphosphine)chlororhodium. The article \u300aRegioselective \u03b2-Trifluoromethylation of \u03b2-Silylporphyrins by Using a Trifluoromethyl Copper Complex\u300b in relation to this compound, is published in European Journal of Organic Chemistry. Let's take a look at the latest research on this compound (cas:1300746-79-5).","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=9465","og_locale":"en_US","og_type":"article","og_title":"The effect of the change of synthetic route on the product 1300746-79-5 | pyrazoles-derivatives","og_description":"The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: (1,10-Phenanthroline)(trifluoromethyl)copper(I)(SMILESS: F[C-](F)([Cu+]1[N]2=C3C4=[N]1C=CC=C4C=CC3=CC=C2)F,cas:1300746-79-5) is researched.Name: Tris(triphenylphosphine)chlororhodium. The article \u300aRegioselective \u03b2-Trifluoromethylation of \u03b2-Silylporphyrins by Using a Trifluoromethyl Copper Complex\u300b in relation to this compound, is published in European Journal of Organic Chemistry. Let's take a look at the latest research on this compound (cas:1300746-79-5).","og_url":"https:\/\/www.pyrazoles-derivatives.com\/?p=9465","og_site_name":"pyrazoles-derivatives","article_published_time":"2022-04-01T03:50:48+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=9465","url":"https:\/\/www.pyrazoles-derivatives.com\/?p=9465","name":"The effect of the change of synthetic route on the product 1300746-79-5 | pyrazoles-derivatives","isPartOf":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/#website"},"datePublished":"2022-04-01T03:50:48+00:00","author":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1"},"description":"The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. 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Let's take a look at the latest research on this compound (cas:1300746-79-5).","breadcrumb":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=9465#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.pyrazoles-derivatives.com\/?p=9465"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=9465#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"\u9996\u9875","item":"https:\/\/www.pyrazoles-derivatives.com\/"},{"@type":"ListItem","position":2,"name":"The effect of the change of synthetic route on the product 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. 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