Latha Rani Nagaraju, Lakshmi Ranganatha Venkataravanappa, S. Anandalwar, S. Khanum
{"title":"N-(2-氨基苯基)-2-甲基苯酰胺的合成、x射线晶体结构研究、Hirshfeld表面分析及生物活性研究","authors":"Latha Rani Nagaraju, Lakshmi Ranganatha Venkataravanappa, S. Anandalwar, S. Khanum","doi":"10.1155/2016/5951013","DOIUrl":null,"url":null,"abstract":"The title compound crystallizes in monoclinic crystal system, with space group . The compound exhibits intermolecular interactions of the types N–H⋯N, C–H⋯O, and C–H⋯π; intramolecular interactions of the type N–H⋯N. The intercontacts are also studied using Hirshfeld surface analysis. The compound showed no remarkable antibacterial activity when screened against two gram-negative and two gram-positive bacteria.","PeriodicalId":15303,"journal":{"name":"Journal of Chemical Technology & Biotechnology","volume":"23 1","pages":"1-7"},"PeriodicalIF":0.0000,"publicationDate":"2016-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Synthesis, X-Ray Crystal Structure Study, Hirshfeld Surface Analysis, and Biological Activity of N-(2-amino-phenyl)-2-methyl-benzamide\",\"authors\":\"Latha Rani Nagaraju, Lakshmi Ranganatha Venkataravanappa, S. Anandalwar, S. Khanum\",\"doi\":\"10.1155/2016/5951013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The title compound crystallizes in monoclinic crystal system, with space group . The compound exhibits intermolecular interactions of the types N–H⋯N, C–H⋯O, and C–H⋯π; intramolecular interactions of the type N–H⋯N. The intercontacts are also studied using Hirshfeld surface analysis. The compound showed no remarkable antibacterial activity when screened against two gram-negative and two gram-positive bacteria.\",\"PeriodicalId\":15303,\"journal\":{\"name\":\"Journal of Chemical Technology & Biotechnology\",\"volume\":\"23 1\",\"pages\":\"1-7\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-11-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Technology & Biotechnology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2016/5951013\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Technology & Biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2016/5951013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis, X-Ray Crystal Structure Study, Hirshfeld Surface Analysis, and Biological Activity of N-(2-amino-phenyl)-2-methyl-benzamide
The title compound crystallizes in monoclinic crystal system, with space group . The compound exhibits intermolecular interactions of the types N–H⋯N, C–H⋯O, and C–H⋯π; intramolecular interactions of the type N–H⋯N. The intercontacts are also studied using Hirshfeld surface analysis. The compound showed no remarkable antibacterial activity when screened against two gram-negative and two gram-positive bacteria.
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