{"id":11237,"date":"2022-11-21T05:06:50","date_gmt":"2022-11-20T21:06:50","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11237"},"modified":"2022-11-21T05:06:50","modified_gmt":"2022-11-20T21:06:50","slug":"zhang-pengfeis-team-published-research-in-asian-journal-of-chemistry-in-26-cas-4551-69-3","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11237","title":{"rendered":"Zhang, Pengfei&#8217;s team published research in Asian Journal of Chemistry  in 26 | CAS: 4551-69-3"},"content":{"rendered":"<p>Zhang, Pengfei published the artcile<b><i>Synthesis, crystal structure and quantum chemistry calculation of two novel compounds derived from amino-phenol<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/4551-69-3.html\">Synthetic Route of 4551-69-3<\/a>,  the publication is  Asian Journal of Chemistry (2014), 26(18), 6176-6184, database is CAplus.<\/p>\n<p>Two novel compounds [(Z)-3-(2-hydroxy-4-methylphenylimino)indolin-2-one][methanol] (A) and 4-[(Z)-(3-hydroxy-4-methoxyphenylimino)(phenyl)methyl]-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one (B) derived from aminophenol were synthesized and characterized by IR spectroscopy, elemental anal. and X-ray diffraction single-crystal anal. Compound A crystallized in monoclinic space group P21\/c with a = 15.6637 (12) \u00b0, b = 12.3527 (9) \u00b0, c = 7.4461 (6) \u00b0, \u03b1 = 90\u00b0, \u03b2 = 100.9460 (10)\u00b0, \u03b3 = 90\u00b0, V = 1414.53 (19) nm<sup>3<\/sup>, Z = 4, F (000) = 600, S = 1.055, R<sub>1<\/sub> = 0392, wR<sub>2<\/sub> = 0.0967. Compound B crystallized in triclinic, space group P-1 with a = 8.8111 (9) \u00b0, b = 11.4716 (12) \u00b0, c = 11.4947 (14) \u00b0, \u03b1 = 115.376 (2)\u00b0, \u03b2 = 99.5470 (10)\u00b0, \u03b3 = 97.6320 (10)\u00b0, V = 1007.74 (19) nm<sup>3<\/sup>, Z = 2, F (000) = 420, S = 1.046, R<sub>1<\/sub> = 0.0643, wR<sub>2<\/sub> = 0.1479. Theor. studies of compounds A and B were carried out by d. functional theory B3LYP method. The results showed that N (1), O (1) and O (2) of compound A and N (3), O (1) and O (2) of compound B were major active sites. Furthermore, N (1) in compound A was preferentially attacked by nucleophilic, followed by the N (3) in compound B. The theor. studies showed that compound A may have higher biol. activity, such as anti-proliferative activity, compared with compound B. The result might be because that compound A was Schiff base and compound B showed proton transfer and tautomerism.<\/p>\n<p>Asian Journal of Chemistry published new progress about 4551-69-3. 4551-69-3 belongs to pyrazoles-derivatives, auxiliary class Benzenes, name is 4-Benzoyl-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, and the molecular formula is C44H28ClFeN4, <a href=\"https:\/\/www.ambeed.com\/products\/4551-69-3.html\">Synthetic Route of 4551-69-3<\/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>Asian Journal of Chemistry published new progress about 4551-69-3. 4551-69-3 belongs to pyrazoles-derivatives, auxiliary class Benzenes, name is 4-Benzoyl-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, and the molecular formula is C44H28ClFeN4, <a href=\"https:\/\/www.ambeed.com\/products\/4551-69-3.html\">Synthetic Route of 4551-69-3<\/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":[740],"class_list":["post-11237","post","type-post","status-publish","format-standard","hentry","category-pyrazoles-derivatives","tag-m-w250-300"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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