1-chloromethyl-4-(4-trifluoromethyl-phenoxy)-benzene | 111818-34-9

• 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: 1-chloromethyl-4-(4-trifluoromethyl-phenoxy)-benzene
• 英文别名: 4-chloromethyl-(4-trifluoromethyl-phenoxy)-benzene；4-(4-trifluoromethylphenoxy)benzyl chloride；1-(Chloromethyl)-4-(4-(trifluoromethyl)phenoxy)benzene；1-(chloromethyl)-4-[4-(trifluoromethyl)phenoxy]benzene
• CAS: 111818-34-9
• 化学式: C₁₄H₁₀ClF₃O
• 分子量: 286.681
• InChiKey: KZLJUTKKAOCAMQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-chloro-2-propyl-5-sulfanylpyridazin-3-one 、 1-chloromethyl-4-(4-trifluoromethyl-phenoxy)-benzene 、 potassium carbonate 、 N,N-二甲基甲酰胺 生成 4-chloro-2-propyl-5-[[4-[4-(trifluoromethyl)phenoxy]phenyl]methylsulfanyl]pyridazin-3-one
  参考文献：
  名称：

  LEYENDECKER, JOACHIM;THEOBALD, HANS;BUERSTINGHAUS, RAINER;KUENAST, CHRIST+

  摘要：

  DOI：
• 作为产物：
  描述：

  [4-(4-trifluoromethyl-phenoxy)-phenyl]-methanol 在 T406石油添加剂 、 氯化亚砜 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 生成 1-chloromethyl-4-(4-trifluoromethyl-phenoxy)-benzene
  参考文献：
  名称：

  WO2007/39171

  摘要：

  公开号：

文献信息

• Indolyl derivatives as liver-X-receptor (LXR) modulators
  申请人：Dehmlow Henrietta

  公开号：US20050245515A1

  公开（公告）日：2005-11-03

  The invention relates to compounds of formula (I): and pharmaceutically acceptable salts and pharmaceutically acceptable esters thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , A, m, n and p are defined as in claim 1. These compounds can be used as pharmaceutical compositions for the treatment of, for example, diabetes.

  这项发明涉及式(I)的化合物： 以及其药学上可接受的盐和药学上可接受的酯，其中R 1 ，R 2 ，R 3 ，R 4 ，R 5 ，R 6 ，A，m，n和p的定义如权利要求书中所述。 这些化合物可用作治疗糖尿病等疾病的药物组合物。
• Novel aminodicarboxylic acid derivatives having pharmaceutical properties
  申请人：Alonso-Alija Cristina

  公开号：US20060094769A1

  公开（公告）日：2006-05-04

  The invention relates to compounds of formulae (II), (IV), and (VI) as shown below, wherein the several variable groups are as defined in the specification and claims. Processes for making these materials, and methods for using them in the synthesis of compounds for treatment of cardiovascular disorders and fibrotic disorders are also disclosed.

  本发明涉及以下式子（II），（IV）和（VI）的化合物，其中各个变量基团如规范和要求中所定义。还公开了制备这些材料的过程以及将它们用于合成治疗心血管疾病和纤维化疾病的化合物的方法。
• 4-OXY-N-[1,3,4]-THIADIAZOL-2-YL-BENZENE SULFONAMIDES, PHARMACEUTICAL COMPOSITIONS AND METHODS FOR THEIR THERAPEUTIC USE
  申请人：KEIL Stefanie

  公开号：US20090012131A1

  公开（公告）日：2009-01-08

  The present invention comprises 4-Oxy-N-[1,3,4]-thiadiazol-2-yl-benzene sulfonamides, the derivatives thereof and salts thereof as well as processes for their preparation and methods for their use as pharmaceutical compositions. More specifically, the invention relates to 4-oxy-N-[1,3,4]-thiadiazol-2-yl-benzene sulfonamides and to their physiologically acceptable salts and physiologically functional derivatives that exhibit peroxisome proliferator activator receptor (PPAR) PPARalpha, PPARdelta and PPARgamma agonist activity. The compounds themselves are defined by the structure of the formula I, wherein the various unnamed substituents are defined herein. The compounds are suitable for the treatment of disorders of fatty acid metabolism and glucose utilization disorders as well as of disorders in which insulin resistance is involved as well as demyelinating and other neurodegenerative disorders of the central and peripheral nervous system.

  本发明涉及4-Oxy-N-[1,3,4]-噻二唑-2-基苯磺酰胺及其衍生物和盐，以及其制备方法和用作制药组合物的方法。更具体地，本发明涉及4-Oxy-N-[1,3,4]-噻二唑-2-基苯磺酰胺及其生理上可接受的盐和生理上功能性衍生物，其表现出过氧化物酶体增殖激活受体(PPAR) PPARalpha、PPARdelta和PPARgamma激动剂活性。这些化合物的结构由式I定义，其中各未命名的取代基在此定义。这些化合物适用于治疗脂肪酸代谢障碍和葡萄糖利用障碍以及胰岛素抵抗涉及的疾病，以及中枢和周围神经系统的脱髓鞘和其他神经退行性疾病的治疗。
• Indolyl derivatives as liver-x-receptor (LXR) modulators
  申请人：Dehmlow Henrietta

  公开号：US20070099916A1

  公开（公告）日：2007-05-03

  The invention relates to compounds of formula (I): and pharmaceutically acceptable salts and pharmaceutically acceptable esters thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , A, m, n and p are defined as in claim 1 . These compounds can be used as pharmaceutical compositions for the treatment of, for example, diabetes.

  本发明涉及式（I）的化合物及其药学上可接受的盐和酯，其中R1、R2、R3、R4、R5、R6、A、m、n和p如权利要求1中所定义。这些化合物可用作药物组合物，用于治疗例如糖尿病等疾病。
• Novel dicarboxylic acid derivatives with pharmaceutical properties
  申请人：Alonso-Alija Cristina

  公开号：US20080058314A1

  公开（公告）日：2008-03-06

  The present invention relates to the use of compounds of the formula (I) and to their salts and stereoisomers, for the preparation of medicaments for the treatment of cardiovascular disorders.

  本发明涉及使用式(I)的化合物及其盐和立体异构体，用于制备治疗心血管疾病的药物。