{"id":10500,"date":"2022-10-21T06:59:36","date_gmt":"2022-10-20T22:59:36","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=10500"},"modified":"2022-10-21T06:59:36","modified_gmt":"2022-10-20T22:59:36","slug":"li-songs-team-published-research-in-wuji-huaxue-xuebao-in-2018-cas-29004-73-7","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=10500","title":{"rendered":"Li, Song&#8217;s team published research in Wuji Huaxue Xuebao in 2018 | CAS: 29004-73-7"},"content":{"rendered":"<p>In 2018,Wuji Huaxue Xuebao included an article by Li, Song; Gan, Xian-xue; Tang, Liang-fu. <a href=\"https:\/\/www.ambeed.com\/products\/29004-73-7.html\">Quality Control of (3-methyl-1H-pyrazol-5-yl)methanol<\/a>. The article was titled \u300aSyntheses and catalytic properties of metal carbonyl derivatives with hydroxymethyl functionalized pyrazoles\u300b. The information in the text is summarized as follows:<\/p>\n<p>Reaction of tungsten or molybdenum carbonyl with 3(5)-hydroxymethyl-5(3)-methylpyrazole (L1), 4-hydroxymethylpyrazole (L2) and bis(3-hydroxymethyl-5-methylpyrazol-1-yl)methane (L3) yielded complexes LW(CO)5 (L = L1 or L2) and L3M(CO)4 (M = Mo or W), resp. These complexes have been fully characterized by NMR, IR and x-ray crystal structural analyses, indicating that they form 1D or 2D organometallic supramol. architectures through O-H\u00b7\u00b7\u00b7O, N-H\u00b7\u00b7\u00b7O and O-H\u00b7\u00b7\u00b7OC-M hydrogen bonding interactions, and these structures are significantly affected by the relative position of the hydroxymethyl group on the pyrazole ring. In addition, these complexes show moderate catalytic activity for the cyclotrimerization reaction of phenylacetylene. The experimental part of the paper was very detailed, including the reaction process of (3-methyl-1H-pyrazol-5-yl)methanol(cas: 29004-73-7<a href=\"https:\/\/www.ambeed.com\/products\/29004-73-7.html\">Quality Control of (3-methyl-1H-pyrazol-5-yl)methanol<\/a>)<\/p>\n<p>(3-methyl-1H-pyrazol-5-yl)methanol(cas: 29004-73-7) belongs to pyrazoles. Pyrazoles and their related multiring analogs are common elements of a wide variety of bioactive compounds. These ring structures are rare in nature. A consequence of this is that they have previously been thought to be poor moieties to include in potential new drugs. <a href=\"https:\/\/www.ambeed.com\/products\/29004-73-7.html\">Quality Control of (3-methyl-1H-pyrazol-5-yl)methanol<\/a><\/p>\n<p>Referemce:<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>(3-methyl-1H-pyrazol-5-yl)methanol(cas: 29004-73-7) belongs to pyrazoles. Pyrazoles and their related multiring analogs are common elements of a wide variety of bioactive compounds. These ring structures are rare in nature. A consequence of this is that they have previously been thought to be poor moieties to include in potential new drugs. <a href=\"https:\/\/www.ambeed.com\/products\/29004-73-7.html\">Quality Control of (3-methyl-1H-pyrazol-5-yl)methanol<\/a><\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[622,131],"tags":[128],"class_list":["post-10500","post","type-post","status-publish","format-standard","hentry","category-29004-73-7","category-pyrazoles-derivatives","tag-100-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Li, Song&#039;s team published research in Wuji Huaxue Xuebao in 2018 | CAS: 29004-73-7 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"In 2018,Wuji Huaxue Xuebao included an article by Li, Song; Gan, Xian-xue; Tang, Liang-fu. Quality Control of (3-methyl-1H-pyrazol-5-yl)methanol. The article was titled \u300aSyntheses and catalytic properties of metal carbonyl derivatives with hydroxymethyl functionalized pyrazoles\u300b. The information in the text is summarized as follows:\" \/>\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=10500\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Li, Song&#039;s team published research in Wuji Huaxue Xuebao in 2018 | CAS: 29004-73-7 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"In 2018,Wuji Huaxue Xuebao included an article by Li, Song; Gan, Xian-xue; Tang, Liang-fu. Quality Control of (3-methyl-1H-pyrazol-5-yl)methanol. 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Quality Control of (3-methyl-1H-pyrazol-5-yl)methanol. The article was titled \u300aSyntheses and catalytic properties of metal carbonyl derivatives with hydroxymethyl functionalized pyrazoles\u300b. 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Quality Control of (3-methyl-1H-pyrazol-5-yl)methanol. The article was titled \u300aSyntheses and catalytic properties of metal carbonyl derivatives with hydroxymethyl functionalized pyrazoles\u300b. The information in the text is summarized as follows:","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=10500","og_locale":"en_US","og_type":"article","og_title":"Li, Song's team published research in Wuji Huaxue Xuebao in 2018 | CAS: 29004-73-7 | pyrazoles-derivatives","og_description":"In 2018,Wuji Huaxue Xuebao included an article by Li, Song; Gan, Xian-xue; Tang, Liang-fu. Quality Control of (3-methyl-1H-pyrazol-5-yl)methanol. The article was titled \u300aSyntheses and catalytic properties of metal carbonyl derivatives with hydroxymethyl functionalized pyrazoles\u300b. 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