{"id":11142,"date":"2022-11-21T05:00:35","date_gmt":"2022-11-20T21:00:35","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11142"},"modified":"2022-11-21T05:00:35","modified_gmt":"2022-11-20T21:00:35","slug":"pereyaslova-d-g-s-team-published-research-in-ukrainskii-khimicheskii-zhurnal-russian-edition-in-45-cas-71203-35-5","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11142","title":{"rendered":"Pereyaslova, D. G.&#8217;s team published research in Ukrainskii Khimicheskii Zhurnal (Russian Edition)  in 45 | CAS: 71203-35-5"},"content":{"rendered":"<p>Pereyaslova, D. G. published the artcile<b><i>Organic luminophors of the pyrazoline series &#8211; luminescent constituents of fluorescent pigments<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/71203-35-5.html\">Application of 4-(5-(4-Methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide<\/a>,  the publication is  Ukrainskii Khimicheskii Zhurnal (Russian Edition) (1979), 45(6), 553-6, database is CAplus.<\/p>\n<p>The addition of 3-(4-difluoromethylsulfonylphenyl)-1,5-diphenyl-\u0394<sup>2<\/sup>-pyrazoline (<strong>I<\/strong>)  [61102-38-3] to aminosulfonyltoluene-formaldehyde-melamine copolymer (<strong>II<\/strong>)  [39277-28-6] gave a bright yellow fluorescent pigment with strong light absorption at 564 nm. When <strong>I<\/strong> and Rhodamine S  [12627-64-4] were added to <strong>II<\/strong> the resulting orange-red pigment absorbed strongly at 609 nm. Similarly, a green fluorescent pigment was obtained by adding 1,4-bis[1,5-diphenyl-\u0394<sup>2<\/sup>-3-pyrazolinyl]benzene  [71203-34-4] and Direct Lightfast Turquoise K  [50642-57-4] to <strong>II<\/strong>. Other shades of pigments were prepared by adding 1-(4-difluoromethylsulfonylphenyl)-3,5-diphenyl-\u0394<sup>2<\/sup>-pyrazoline  [61102-37-2], or pyrazoline sulfonate <strong>III<\/strong>, X = H, H<sub>2<\/sub>NSO<sub>2<\/sub>, or C<sub>17<\/sub>H<sub>35<\/sub>CONHSO<sub>2<\/sub> (<strong>IV<\/strong>) to <strong>II<\/strong>. The synthesis of <strong>III<\/strong> (X = H) or <strong>III<\/strong> (X = H<sub>2<\/sub>NSO<sub>2<\/sub>) involved reacting sulfonated 4-methoxybenzalacetophenone with PhN:NH  [100-63-0] or 4-H<sub>2<\/sub>NSO<sub>2<\/sub>C<sub>6<\/sub>H<sub>4<\/sub>N:NH  [4392-54-5], resp. Refluxing <strong>III<\/strong> (X = H<sub>2<\/sub>NSO<sub>2<\/sub>) with stearic chloride  [112-76-5] gave <strong>IV<\/strong>.<\/p>\n<p>Ukrainskii Khimicheskii Zhurnal (Russian Edition) published new progress about 71203-35-5. 71203-35-5 belongs to pyrazoles-derivatives, auxiliary class GPCR\/G Protein,Ras, name is 4-(5-(4-Methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide, and the molecular formula is C22H21N3O3S, <a href=\"https:\/\/www.ambeed.com\/products\/71203-35-5.html\">Application of 4-(5-(4-Methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide<\/a>.<\/p>\n<p>Referemce:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">https:\/\/en.wikipedia.org\/wiki\/Pyrazole<\/a>,<br \/><a href=\"Pyrazole - Wikipedia\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Ukrainskii Khimicheskii Zhurnal (Russian Edition) published new progress about 71203-35-5. 71203-35-5 belongs to pyrazoles-derivatives, auxiliary class GPCR\/G Protein,Ras, name is 4-(5-(4-Methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide, and the molecular formula is C22H21N3O3S, <a href=\"https:\/\/www.ambeed.com\/products\/71203-35-5.html\">Application of 4-(5-(4-Methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide<\/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":[785],"class_list":["post-11142","post","type-post","status-publish","format-standard","hentry","category-pyrazoles-derivatives","tag-m-w400-450"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Pereyaslova, D. 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G. published the artcileOrganic luminophors of the pyrazoline series - luminescent constituents of fluorescent pigments, Application of 4-(5-(4-Methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide, the publication is Ukrainskii Khimicheskii Zhurnal (Russian Edition) (1979), 45(6), 553-6, database is CAplus.\",\"breadcrumb\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=11142#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.pyrazoles-derivatives.com\/?p=11142\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=11142#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"\u9996\u9875\",\"item\":\"https:\/\/www.pyrazoles-derivatives.com\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Pereyaslova, D. 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