α-4-Chlorphenoxy-4-chlor-acetophenon | 64009-05-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: α-4-Chlorphenoxy-4-chlor-acetophenon
• 英文别名: 2-(4-chloro-phenoxy)-1-(4-chloro-phenyl)-ethanone；2-(4-Chlor-phenoxy)-1-(4-chlor-phenyl)-aethanon；(4-chlorophenoxymethyl)-(4-chlorophenyl)-ketone；2-(4-Chlorophenoxy)-1-(4-chlorophenyl)ethan-1-one；2-(4-chlorophenoxy)-1-(4-chlorophenyl)ethanone
• CAS: 64009-05-8
• 化学式: C₁₄H₁₀Cl₂O₂
• mdl: MFCD01798389
• 分子量: 281.138
• InChiKey: VTIWQRYGKXRZOH-UHFFFAOYSA-N

物化性质

• 熔点：
  132-133 °C
• 沸点：
  425.9±30.0 °C(Predicted)
• 密度：
  1.318±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.071
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  α-4-Chlorphenoxy-4-chlor-acetophenon 在 吡啶 、 溴 作用下， 以 乙醇 、 氯仿 为溶剂， 反应 5.0h， 生成 7-(4-chlorophenoxy)-6-(4-chlorophenyl)-3-ethyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine
  参考文献：
  名称：

  Chande; Karnik; Inamdar, Journal of the Indian Chemical Society, 1990, vol. 67, # 3, p. 220 - 222

  摘要：

  DOI：
• 作为产物：
  描述：

  对氯苯酚 、 2'-溴-4-氯苯乙酮 在 potassium carbonate 作用下， 以 丙酮 为溶剂， 生成 α-4-Chlorphenoxy-4-chlor-acetophenon
  参考文献：
  名称：

  抗霉菌咪唑。3.1- [2-（芳氧基烷基）-2-苯基乙基] -1H-咪唑的合成和抗真菌性能。

  摘要：

  DOI：

  10.1021/jm00221a033

文献信息

• Indazole derivatives as JNK inhibitors and compositions and methods related thereto
  申请人：Bhagwat S. Shripad

  公开号：US20050107457A1

  公开（公告）日：2005-05-19

  Compounds having activity as selective inhibitors of JNK are disclosed. The compounds of this invention are indazole derivatives having the following structure: wherein R 1 , R 2 and A are as defined herein. Such compounds have utility in the treatment of a wide range of conditions that are responsive to JNK inhibition. Thus, methods of treating such conditions are also disclosed, as are pharmaceutical compositions containing one or more compounds of the above compounds.

  本发明揭示了具有选择性抑制JNK活性的化合物。本发明的化合物是具有以下结构的吲唑衍生物：其中R1、R2和A如本文所定义。这些化合物在治疗对JNK抑制有反应的广泛疾病方面具有实用性。因此，本发明还揭示了治疗这些疾病的方法，以及含有上述化合物中的一个或多个化合物的制药组合物。
• Ketones
  申请人：Barton John Peter

  公开号：US20050272036A1

  公开（公告）日：2005-12-08

  Compounds of formula (I): wherein variable groups are as defined within; for use in the inhibition of 11βHSD1 are described.

  描述了式(I)的化合物：其中变量基团如定义的那样；用于抑制11βHSD1。
• 787. Polymethin dyes from 4 : 5-disubstituted thiazoles
  作者：Edward B. Knott

  DOI：10.1039/jr9520004099

  日期：——
• Unprecedented C-2 arylation of indole with diazonium salts: Syntheses of 2,3-disubstituted indoles and their antimicrobial activity
  作者：Seth Daly、Kathryn Hayden、Indranil Malik、Nikki Porch、Hong Tang、Snezna Rogelj、Liliya V. Frolova、Katrina Lepthien、Alexander Kornienko、Igor V. Magedov

  DOI：10.1016/j.bmcl.2011.06.081

  日期：2011.8

  A novel reaction of indole with aryldiazonium salts leading to the formation of 2-aryl-3-(arylazo)indoles was discovered. The products were found to possess potent anti-MRSA and anti-LLVRE activities. The SAR studies indicate that the potentially metabolically labile azo functionality can be replaced with ether oxygen and thioether sulfur atoms without any loss of activity. (C) 2011 Elsevier Ltd. All rights reserved.
• Antiproliferative activity of 2,3-disubstituted indoles toward apoptosis-resistant cancers cells
  作者：Igor V. Magedov、Florence Lefranc、Liliya V. Frolova、Laetitia Moreno Y. Banuls、Amanda S. Peretti、Snezna Rogelj、Véronique Mathieu、Robert Kiss、Alexander Kornienko

  DOI：10.1016/j.bmcl.2013.03.110

  日期：2013.6

  Many types of cancer, including glioma, melanoma, NSCLC, among others, are resistant to apoptosis induction and poorly responsive to current therapies with propaptotic agents. We describe a series of 2,3-disubstituted indoles, which display cytostatic rather than cytotoxic effects in cancer cells, and serve as a new chemical scaffold to develop anticancer agents capable of combating apoptosis-resistant cancers associated with dismal prognoses. (C) 2013 Elsevier Ltd. All rights reserved.