1-(4-octyl-phenyl)-propan-1-one | 79219-18-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-(4-octyl-phenyl)-propan-1-one
• 英文别名: 1-(4-Octyl-phenyl)-propan-1-on；1-(4-Octylphenyl)propan-1-one
• CAS: 79219-18-4
• 化学式: C₁₇H₂₆O
• 分子量: 246.393
• InChiKey: JNYGRBAJMGFWPJ-UHFFFAOYSA-N

物化性质

• 沸点：
  356.3±21.0 °C(Predicted)
• 密度：
  0.914±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  18
• 可旋转键数：
  9
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-(4-octyl-phenyl)-propan-1-one 在 盐酸 、 亚硝酸异丙酯 作用下， 以 乙醚 为溶剂， 反应 2.0h， 生成 1-(4-Octyl-phenyl)-propane-1,2-dione 2-oxime
  参考文献：
  名称：

  Beger, J.; Thielemann, C., Journal fur praktische Chemie (Leipzig 1954), 1981, vol. 323, # 1, p. 137 - 148

  摘要：

  DOI：
• 作为产物：
  描述：

  1-苯基辛烷 、 丙酰氯 在 三氯化铝 作用下， 以 二氯甲烷 为溶剂， 生成 1-(4-octyl-phenyl)-propan-1-one
  参考文献：
  名称：

  5-Aryl-imidazolin-2-ones as a scaffold for potent antioxidant and memory-improving activity

  摘要：

  A series of 5-phenyl-substituted-N-alkyl-imidazolin-2-ones with potent radical-scavenging activity and lipid peroxidation inhibitory activity was synthesized. Many of the compounds showed memory-improving effect in animal models independent of the inhibitory activity on lipid peroxidation. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.12.064

文献信息

• NOVEL ANTIBACTERIAL AGENTS FOR THE TREATMENT OF GRAM POSITIVE INFECTIONS
  申请人：MetCalf, III Chester A.

  公开号：US20100184649A1

  公开（公告）日：2010-07-22

  The present invention relates to novel lipopeptide compounds, pharmaceutical compositions of these compounds and methods of using these compounds as antibacterial compounds. The compounds of the invention are particularly useful against a variety of bacteria, including resistant strains. The compounds are useful as antibacterial agents against Clostridium difficile.

  本发明涉及新型脂肽化合物，这些化合物的药物组合物以及使用这些化合物作为抗菌化合物的方法。本发明的化合物特别适用于对抗各种细菌，包括耐药菌株。这些化合物可用作抗Clostridium difficile的抗菌剂。
• Ueda et al., Pharmaceutical Bulletin, 1956, vol. 4, p. 182,184
  作者：Ueda et al.

  DOI：——

  日期：——
• BEGER J.; THIELEMANN C., J. PRAKT. CHEM., 1981, 323, NO 1, 137-148
  作者：BEGER J.、 THIELEMANN C.

  DOI：——

  日期：——
• PREPARATION OF FINGOLIMOD AND ITS SALTS
  申请人：Dr. Reddy's Laboratories Ltd.

  公开号：EP2702034A2

  公开（公告）日：2014-03-05
• Prodrugs of NH-Acidic Compounds: Ester, Carbonate, Carbamate and Phosphonate Derivatives
  申请人：Alkermes Pharma Ireland Limited

  公开号：US20170196848A1

  公开（公告）日：2017-07-13

  The invention provides a method of sustained delivery of a lactam, imide, amide, sulfonamide, carbamate or urea containing parent drug by administering to a patient an effective amount of a prodrug compound of the invention wherein upon administration to the patient, release of the parent drug from the prodrug is sustained release. Prodrug compounds suitable for use in the methods of the invention are labile conjugates of parent drugs that are derivatized through carbonyl linked prodrug moieties. The prodrug compounds of the invention can be used to treat any condition for which the lactam, imide, amide, sulfonamide, carbamate or urea containing parent drug is useful as a treatment.