4-Nitro-2-phenyl-1H-imidazole | 4308-29-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 4-Nitro-2-phenyl-1H-imidazole
• 英文别名: 5-nitro-2-phenyl-1H-imidazole
• CAS: 4308-29-6
• 化学式: C₉H₇N₃O₂
• 分子量: 189.173
• InChiKey: OIIFBUDLPDQPRC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  74.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  4-苯基咪唑 、 硝酸 生成 4-Nitro-2-phenyl-1H-imidazole
  参考文献：
  名称：

  HURST, DEREK T., HETEROCYCLES, 27,(1988) N, C. 371-376

  摘要：

  DOI：

文献信息

• [EN] DIAZABICYCLONONENE AND TETRAHYDROPYRIDINE DERIVATIVES AS RENIN INHIBITORS<br/>[FR] DERIVES DE DIAZABICYCLONONENE ET DE TETRAHYDROPYRIDINE UTILISES COMME INHIBITEURS DE LA RENINE
  申请人：ACTELION PHARMACEUTICALS LTD

  公开号：WO2004096804A1

  公开（公告）日：2004-11-11

  The invention relates to novel 3,9-diazabicyclo[3.3.1]nonene derivatives, tetrahydropyridine derivatives, and related compounds and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as inhibitors of renin.

  本发明涉及新型的3,9-二氮杂双环[3.3.1]壬烯衍生物、四氢吡啶衍生物及其相关化合物，以及它们作为活性成分用于制备药物组合物的用途。本发明还涉及相关方面，包括制备这些化合物的方法、含有一种或多种这些化合物的药物组合物，尤其是它们作为肾素抑制剂的用途。
• [EN] KINASE INHIBITORS<br/>[FR] INHIBITEURS DE LA KINASE
  申请人：LILLY CO ELI

  公开号：WO2005080380A1

  公开（公告）日：2005-09-01

  ABSTRACT The present invention provides kinase inhibitors of Formula I: .

  摘要 本发明提供了化合物I的激酶抑制剂。
• [EN] LXR MODULATORS<br/>[FR] MODULATEURS DES LXR
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2014144037A1

  公开（公告）日：2014-09-18

  The present invention provides compounds of Formula I: and pharmaceutically acceptable salts or solvates thereof, as modulators of liver X receptors (LXR), compositions comprising any of such novel compounds, methods of using these compounds or compositions as medicaments for prevention or treatment of diseases or disorders related to liver X receptor (LXR), as well as methods of preparing these LXR modulators and using them in the manufacture of medicaments.

  本发明提供了式I的化合物及其药学上可接受的盐或溶剂化合物，作为肝X受体（LXR）的调节剂，包括任何此类新化合物的组合物，使用这些化合物或组合物作为预防或治疗与肝X受体（LXR）相关的疾病或紊乱的药物的方法，以及制备这些LXR调节剂的方法，并将它们用于药物的制造。
• Electrooptic chromophores with large optical birefringence for applications at high speed and short wavelengths
  申请人：McGinniss D. Vincent

  公开号：US20060106262A1

  公开（公告）日：2006-05-18

  Disclosed is a series of materials, which exhibit large birefringence under the influence of an applied electric field. These materials are capable of switching this large birefringence with a characteristic time on the order of 1 microsecond or less. In addition, these materials have good optical loss at this wavelength, and are stable under irradiation. These materials are suitable for fabrication of optical devices such a variable optical attenuators, switches, and modulators that respond in these time frames or slower. These materials are also suitable for use across a wide range of wavelengths. As a second component of this invention, some of these novel materials exhibit these desired optical properties (large birefringence, low loss, stability under illumination) at wavelengths as short as about 400 nm. These materials are suitable for fabrication of optical devices operating at or about 405 nm, where conventional EO materials strongly absorb and/or quickly degrade.

  披露了一系列材料，这些材料在受到外加电场影响下表现出较大的双折射。这些材料能够在大约1微秒或更短的时间内切换这种较大的双折射。此外，这些材料在这个波长下具有良好的光学损耗，并且在辐照下稳定。这些材料适用于制造像可变光学衰减器、开关和调制器等在这些时间范围或更慢响应的光学器件。这些材料也适用于在广泛波长范围内使用。作为本发明的第二个组成部分，一些新型材料在约400纳米的波长下展现出这些理想的光学特性（较大的双折射、低损耗、辐照下的稳定性）。这些材料适用于制造在或约405纳米波长下运行的光学器件，传统的电光材料在这个波长下会强烈吸收和/或迅速降解。
• Ortho-heterocyclic substituted aryl amides for controlling invertebrate pests
  申请人：——

  公开号：US20040242645A1

  公开（公告）日：2004-12-02

  This invention pertains to compounds of Formula I, their N-oxides and suitable salts (Formula I) wherein A is O or S; G is a 5- or 6-membered heteroaromatic ring or a 5- or 6-membered nonaromatic heterocyclic ring optionally including one or two ring members selected from the group consisting of C(═O), SO or S(O) 2 , each ring optionally substituted with from one to four R 2 ; each J is independently a phenyl ring, a 5- or 6-membered heteroaromatic ring or an aromatic 8-, 9- or 10-membered fused carbobicyclic or heterobicyclic ring system, wherein each ring or ring system is optionally substituted with from one to four R 3 ; and R 1 , R 2 , R 3 , R 4 and n are as defined in the disclosure. Also disclosed are methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of Formula I, an N-oxide thereof or a suitable salt of the compound (e.g., as a composition described herein). This invention also pertains to a composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of Formula I, an N-oxide thereof or a suitable salt of the compound and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents. 1

  本发明涉及式I的化合物，其N-氧化物和适宜的盐（式I）其中A是O或S; G是5-或6-成员杂芳环或5-或6-成员非芳杂环，可选地包括一个或两个环成员，所选自C（═O），SO或S（O）2的群，每个环可选地取代1-4个R2; 每个J是独立的苯环，5-或6-成员杂芳环或芳香8-、9-或10-成员融合碳杂双环系统，其中每个环或环系统可选地取代1-4个R3; R1、R2、R3、R4和n如本公开说明中所定义。本发明还公开了一种控制无脊椎动物害虫的方法，包括将无脊椎动物害虫或其环境与式I的化合物，其N-氧化物或化合物的适宜盐的生物有效量接触（例如，作为本文所述的组合物）。本发明还涉及一种用于控制无脊椎动物害虫的组合物，其包括式I的化合物、其N-氧化物或化合物的适宜盐的生物有效量和至少一种来自表面活性剂、固体稀释剂和液体稀释剂的群体中选择的其他成分。