{"id":10426,"date":"2022-10-21T06:57:22","date_gmt":"2022-10-20T22:57:22","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=10426"},"modified":"2022-10-21T06:57:22","modified_gmt":"2022-10-20T22:57:22","slug":"diez-barra-e-s-team-published-research-in-synthetic-communications-in-1990-cas-52096-24-9-2","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=10426","title":{"rendered":"Diez-Barra, E.&#8217;s team published research in Synthetic Communications in 1990 | CAS: 52096-24-9"},"content":{"rendered":"<p><a href=\"https:\/\/www.ambeed.com\/products\/52096-24-9.html\">Safety of 1-Butyl-1H-pyrazole<\/a>On September 30, 1990 ,\u300aSynthesis of N-alkylpyrazoles by phase transfer catalysis without solvent\u300b was published in Synthetic Communications. The article was written by Diez-Barra, E.; De la Hoz, A.; Sanchez-Migallon, A.; Tejeda, J.. The article contains the following contents:<\/p>\n<p>The reaction of alkyl halides with pyrazoles in the presence of Bu4N+ Br- without solvent gave 36-98% N-alkylpyrazoles I [R = Me(CH2)n, PhCH2, CH2:CHCH2, CH2:C:CH; n = 0, 1, 3, 7, 15].1-Butyl-1H-pyrazole(cas: 52096-24-9<a href=\"https:\/\/www.ambeed.com\/products\/52096-24-9.html\">Safety of 1-Butyl-1H-pyrazole<\/a>) was used in this study.<\/p>\n<p>1-Butyl-1H-pyrazole(cas: 52096-24-9) 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\/52096-24-9.html\">Safety of 1-Butyl-1H-pyrazole<\/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>1-Butyl-1H-pyrazole(cas: 52096-24-9) 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\/52096-24-9.html\">Safety of 1-Butyl-1H-pyrazole<\/a><\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[687,131],"tags":[128],"class_list":["post-10426","post","type-post","status-publish","format-standard","hentry","category-52096-24-9","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>Diez-Barra, E.&#039;s team published research in Synthetic Communications in 1990 | CAS: 52096-24-9 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Safety of 1-Butyl-1H-pyrazoleOn September 30, 1990 ,\u300aSynthesis of N-alkylpyrazoles by phase transfer catalysis without solvent\u300b was published in Synthetic Communications. The article was written by Diez-Barra, E.; De la Hoz, A.; Sanchez-Migallon, A.; Tejeda, J.. The article contains the following contents:\" \/>\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=10426\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Diez-Barra, E.&#039;s team published research in Synthetic Communications in 1990 | CAS: 52096-24-9 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"Safety of 1-Butyl-1H-pyrazoleOn September 30, 1990 ,\u300aSynthesis of N-alkylpyrazoles by phase transfer catalysis without solvent\u300b was published in Synthetic Communications. The article was written by Diez-Barra, E.; De la Hoz, A.; Sanchez-Migallon, A.; Tejeda, J.. 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