4'-aminodecanoylphenone | 101449-24-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4'-aminodecanoylphenone
• 英文别名: <4-Amino-phenyl>-nonyl-Keton；1-(4-amino-phenyl)-decan-1-one；1-(4-Amino-phenyl)-decan-1-on；1-(4-Aminophenyl)decan-1-one
• CAS: 101449-24-5
• 化学式: C₁₆H₂₅NO
• 分子量: 247.381
• InChiKey: BWJOGQIQKPFJSE-UHFFFAOYSA-N

物化性质

• 熔点：
  96 °C
• 沸点：
  398.4±15.0 °C(Predicted)
• 密度：
  0.968±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  18
• 可旋转键数：
  9
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  43.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4'-aminodecanoylphenone 在 氢氧化钾 、 一水合肼 、 二乙二醇 作用下， 生成 4-癸基苯胺
  参考文献：
  名称：

  Ogawa, Technology Reports of Kansai University, 1959, # 1, p. 41,43, 44

  摘要：

  DOI：
• 作为产物：
  描述：

  acetic acid-(4-decanoyl-anilide) 在 盐酸 作用下， 生成 4'-aminodecanoylphenone
  参考文献：
  名称：

  Kosuge; Sato, Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan, 1954, vol. 74, p. 1139

  摘要：

  DOI：

文献信息

• Process for making diarylamines
  申请人：UNIROYAL, INC.

  公开号：EP0103990A1

  公开（公告）日：1984-03-28

  An improved process for preparing diarylamines from alicyclic ketones, a primary aromatic amine, and a hydrogen acceptor, in the presence of a platinum metal catalyst and an acid promoter.

  一种改进的工艺，在铂金属催化剂和酸促进剂存在下，由脂环酮、芳香族伯胺和氢受体制备二芳基胺。
• Synthesis and methemoglobinemia-inducing properties of analogues of para-aminopropiophenone designed as humane rodenticides
  作者：David Rennison、Daniel Conole、Malcolm D. Tingle、Junpeng Yang、Charles T. Eason、Margaret A. Brimble

  DOI：10.1016/j.bmcl.2013.10.046

  日期：2013.12

  A number of structural analogues of the known toxicant para-aminopropiophenone (PAPP) have been prepared and evaluated for their capacity to induce methemoglobinemia-with a view to their possible application as humane pest control agents. It was found that an optimal lipophilicity for the formation of methemoglobin (metHb) in vitro existed for alkyl analogues of PAPP (aminophenones 1-20; compound 6 metHb% = 74.1 +/- 2). Besides lipophilicity, this structural sub-class suggested there were certain structural requirements for activity, with both branched (10-16) and cyclic (17-20) alkyl analogues exhibiting inferior in vitro metHb induction. Of the four candidates (compounds 4, 6, 13 and 23) evaluated in vivo, 4 exhibited the greatest toxicity. In parallel, aminophenone bioisosteres, including oximes 30-32, sulfoxide 33, sulfone 34 and sulfonamides 35-36, were found to be inferior metHb inducers to lead ketone 4. Closer examination of Hammett substituent constants suggests that a particular combination of the field and resonance parameters may be significant with respect to the redox mechanisms behind PAPPs metHb toxicity. (C) 2013 Elsevier Ltd. All rights reserved.
• Nikolenko et al., Zhurnal Obshchei Khimii, 1960, vol. 30, p. 1028; engl. Ausg. S. 1042
  作者：Nikolenko et al.

  DOI：——

  日期：——
• US4167509A
  申请人：——

  公开号：US4167509A

  公开（公告）日：1979-09-11
• US4431841A
  申请人：——

  公开号：US4431841A

  公开（公告）日：1984-02-14

表征谱图