N,Na(2)-Bis[4-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)phenyl]urea | 112566-88-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯啉
• 英文名称: N,Na(2)-Bis[4-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)phenyl]urea
• 英文别名: 1,3-bis[4-(2,5-dioxopyrrol-1-yl)phenyl]urea
• CAS: 112566-88-8
• 化学式: C₂₁H₁₄N₄O₅
• 分子量: 402.4
• InChiKey: HOONDDIVFWBNDE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  30
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  116
• 氢给体数：
  2
• 氢受体数：
  5

文献信息

• Covalent methods for immobilization of thiolated biomolecules on siliceous and metallic surfaces
  申请人：Levicky Rastislav

  公开号：US20070072199A1

  公开（公告）日：2007-03-29

  The present invention is directed to methods for immobilizing molecules on siliceous and metallic surfaces. Molecules are immobilized on siliceous or metallic surfaces by stable covalent linkages that are capable of withstanding prolonged use and elevated temperatures. Further, the methods of the present invention describe less-complicated chemistries for the immobilization of molecules that will benefit the reproducibility, efficiency and effectiveness of applications in sensing, chromatography, medical diagnostics and related areas where specific recognition between immobilized and free molecules provides diagnostic information or serves as part of a purification or separations process.
• [EN] COVALENT METHODS FOR IMMOBILIZATION OF THIOLATED BIOMOLECULES ON SILICEOUS AND METALLIC SURFACES<br/>[FR] PROCEDES COVALENTS D'IMMOBILISATION DE BIOMOLECULES THIOLEES SUR DES SURFACES SILICEUSES ET METALLIQUES
  申请人：UNIV COLUMBIA

  公开号：WO2004113872A2

  公开（公告）日：2004-12-29

  The present invention is directed to methods for immobilizing molecules on siliceous and metallic surfaces. Molecules are immobilized on siliceous or metallic surfaces by stable covalent linkages that are capable of withstanding prolonged use and elevated temperatures. Further, the methods of the present invention describe less-complicated chemistries for the immobilization of molecules that will benefit the reproducibility, efficiency and effectiveness of applications in sensing, chromatography, medical diagnostics and related areas where specific recognition between immobilized and free molecules provides diagnostic information or serves as part of a purification or separations process.