3-bromodinitrobenzene | 13296-65-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3-bromodinitrobenzene
• 英文别名: 2-Brom-1,4-dinitro-benzol；2,5-Dinitro-brombenzol；2-bromo-1,4-dinitro-benzene；p-Dinitrobrombenzol；2-bromo-1,4-dinitrobenzene
• CAS: 13296-65-6
• 化学式: C₆H₃BrN₂O₄
• 分子量: 247.005
• InChiKey: UNKBAZOGFJAXHC-UHFFFAOYSA-N

物化性质

• 熔点：
  70 °C
• 沸点：
  303.8±22.0 °C(Predicted)
• 密度：
  1.910±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  91.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-bromodinitrobenzene 在 盐酸 、 tin 作用下， 生成 [1,4]benzoquinone-bis-(2,5-diamino-phenylimine)
  参考文献：
  名称：

  STRUCTURE OF THE BANDROWSKI BASE. II. N,N'-BIS-(2,5-DIAMINOPHENYL)-p-QUINONEDIIMINE

  摘要：

  DOI：

  10.1021/jo01138a014
• 作为产物：
  描述：

  2-bromo-4-nitro-1-nitroso-benzene 在 硝酸 作用下， 生成 3-bromodinitrobenzene
  参考文献：
  名称：

  STRUCTURE OF THE BANDROWSKI BASE. II. N,N'-BIS-(2,5-DIAMINOPHENYL)-p-QUINONEDIIMINE

  摘要：

  DOI：

  10.1021/jo01138a014

文献信息

• [EN] DEOXYNOJIRIMYCIN DERIVATIVES AS GLUCOSIDASE INHIBITORS<br/>[FR] DÉRIVÉS DE DÉSOXYNOJIRIMYCINE EN TANT QU'INHIBITEURS DE GLUCOSIDASE
  申请人：EMERGENT PRODUCT DEV GAITHERSBURG INC

  公开号：WO2022011211A1

  公开（公告）日：2022-01-13

  The present application provides novel iminosugars and their use as glucosidase inhibitors. The present inventors have discovered that certain deoxynojirimycin derivatives may be effective in inhibiting glucosidases. In particular, such deoxynojirimycin derivatives may be useful for treating a disease or condition where inhibiting glucosidase may be important.

  本申请提供了新颖的亚胺糖以及它们作为葡萄糖苷酶抑制剂的用途。本发明人发现某些脱氧诺吉霉素衍生物可能有效地抑制葡萄糖苷酶。特别是，这些脱氧诺吉霉素衍生物可能对治疗需要抑制葡萄糖苷酶的疾病或病况有用。
• Koerner; Contardi, Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti, 1914, vol. <5> 23 I, p. 283
  作者：Koerner、Contardi

  DOI：——

  日期：——
• FUNCTIONALIZED EXPANDED PORPHYRINS
  申请人：Sessler Jonathan L.

  公开号：US20100197031A1

  公开（公告）日：2010-08-05

  Disclosed are functionalized expanded porphyrins that can be used as spectrometric sensors for high-valent actinide cations. The disclosed functionalized expanded porphyrins have the advantage over unfunctionalized systems in that they can be immobilized via covalent attachment to a solid support comprising an inorganic or organic polymer or other common substrates. Substrates comprising the disclosed functionalized expanded porphyrins are also disclosed. Further, disclosed are methods of making the disclosed compounds (immobilized and free), methods of using them as sensors to detect high valent actinides, devices that comprise the disclosed compounds, and kits.
• US8580845B2
  申请人：——

  公开号：US8580845B2

  公开（公告）日：2013-11-12
• [EN] FUNCTIONALIZED EXPANDED PORPHYRINS<br/>[FR] PORPHYRINES EXPANSÉES FONCTIONNALISÉES
  申请人：UNIV TEXAS

  公开号：WO2009006075A2

  公开（公告）日：2009-01-08

  Disclosed are functionalized expanded porphyrins that can be used as spectrometric sensors for high-valent actinide cations. The disclosed functionalized expanded porphyrins have the advantage over unfunctionalized systems in that they can be immobilized via covalent attachment to a solid support comprising an inorganic or organic polymer or other common substrates. Substrates comprising the disclosed functionalized expanded porphyrins are also disclosed. Further, disclosed are methods of making the disclosed compounds (immobilized and free), methods of using them as sensors to detect high valent actinides, devices that comprise the disclosed compounds, and kits.