7-oxo-2-propyloctanoic acid | 85054-86-0

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 7-oxo-2-propyloctanoic acid
• CAS: 85054-86-0
• 化学式: C₁₁H₂₀O₃
• 分子量: 200.278
• InChiKey: IGAVHVDDOYJXNZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  14
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.82
• 拓扑面积：
  54.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  8-methyl-2-nonanone 、 一氧化碳 在 氢氟酸 、 五氟化锑 作用下， 反应 3.0h， 生成 2,2-Dimethyl-8-oxo-nonanoic acid 、 7-oxo-2-propyloctanoic acid 、 2-Methyl-9-oxo-decanoic acid 、 2-Ethyl-8-oxo-nonanoic acid
  参考文献：
  名称：

  碳-碳和碳-氢键在超强酸中的反应行为。一氧化碳和水对烷基甲基酮的羧化

  摘要：

  在 HF-SbF5 溶液中，在-20~30 °C 的大气压下，具有五个或更多碳原子的烷基的酮反应生成相应的氧代羧酸，而没有任何β-断裂过程，而β-断裂过程很容易发生在由以下方法衍生的烷基阳离子中具有七个或更多碳原子的烷烃的质子分解。位于 δ 处或远离底物中氧代基团的叔 C-H 键可以在 -20°C 下专门反应生成 (ω-1)-氧代-2,2-二甲基羧酸。

  DOI：

  10.1246/cl.1983.19

文献信息

• NERVE REGENERATION PROMOTERS
  申请人：ONO PHARMACEUTICAL CO., LTD.

  公开号：EP1685832A1

  公开（公告）日：2006-08-02

  A nerve regeneration which comprises a compound is represented by formula (I): (wherein all symbols are shown in the description), a salt thereof or a prodrug thereof. The compound of the present invention is suppresses nerve cell death as a substance for accelerating growth and/or differentiation of stem cells (nerve stem cells, embryonic stem cells, bone marrow cells, etc.), a substance for accelerating growth and/or differentiation of nerve precursor cells, a potentiator for neurotrophic factor activity, a neurotrophic factor-like substance or a neurodegenerative suppressor, and accelerates repair and regeneration of nerve tissues by neogenesis, regeneration and/or axon evolution. In addition, the compound of the present invention is useful for preparation from brain tissues, bone marrow and/or embryonic stem cells of cells for transplant (nerve stem cells, nerve precursor cells, nerve cells, etc.) and also accelerates grafting, growth, differentiation and/or function expression of cells for transplant whereupon it is useful for prevention and/or treatment of neurodegenerative diseases.

  由式 (I) 所表示的化合物组成的神经再生剂： (其中所有符号均在描述中显示）、其盐或其原药。本发明化合物可抑制神经细胞死亡，可作为加速干细胞（神经干细胞、胚胎干细胞、骨髓细胞等）生长和/或分化的物质、加速神经前体细胞生长和/或分化的物质、神经营养因子活性增效剂、神经营养因子样物质或神经退行性抑制剂，并通过新生、再生和/或轴突演化加速神经组织的修复和再生。此外，本发明的化合物可用于从脑组织、骨髓和/或胚胎干细胞中制备移植细胞（神经干细胞、神经前体细胞、神经细胞等），还可加速移植细胞的移植、生长、分化和/或功能表达，从而可用于预防和/或治疗神经退行性疾病。
• Nerve regeneration promoters
  申请人：Tateishi Narito

  公开号：US20070043114A1

  公开（公告）日：2007-02-22

  A nerve regeneration which comprises a compound is represented by formula (I): (wherein all symbols are shown in the description), a salt thereof or a prodrug thereof. The compound of the present invention is suppresses nerve cell death as a substance for accelerating growth and/or differentiation of stem cells (nerve stem cells, embryonic stem cells, bone marrow cells, etc.), a substance for accelerating growth and/or differentiation of nerve precursor cells, a potentiator for neurotrophic factor activity, a neurotrophic factor-like substance or a neurodegenerative suppressor, and accelerates repair and regeneration of nerve tissues by neogenesis, regeneration and/or axon evolution. In addition, the compound of the present invention is useful for preparation from brain tissues, bone marrow and/or embryonic stem cells of cells for transplant (nerve stem cells, nerve precursor cells, nerve cells, etc.) and also accelerates grafting, growth, differentiation and/or function expression of cells for transplant whereupon it is useful for prevention and/or treatment of neurodegenerative diseases.
• US8569058B2
  申请人：——

  公开号：US8569058B2

  公开（公告）日：2013-10-29
• REACTION BEHAVIOR OF CARBON–CARBON AND CARBON–HYDROGEN BONDS IN SUPER ACIDS. CARBOXYLATION OF ALKYL METHYL KETONES WITH CARBON MONOXIDE AND WATER
  作者：Norihiko Yoneda、Haruhiko Sato、Tsuyoshi Fukuhara、Yukio Takahashi、Akira Suzuki

  DOI：10.1246/cl.1983.19

  日期：1983.1.5

  In a HF–SbF5 solution at −20∼30 °C under atmospheric pressure, ketones having alkyl groups with five or more carbon atoms underwent the reaction to give corresponding oxo carboxylic acids without any β-scission processes which occur readily in alkyl cations derived by protolysis of alkanes with seven or more carbon atoms. Tertiary C–H bond located at δ or further away from the oxo group in the substrates

  在 HF-SbF5 溶液中，在-20~30 °C 的大气压下，具有五个或更多碳原子的烷基的酮反应生成相应的氧代羧酸，而没有任何β-断裂过程，而β-断裂过程很容易发生在由以下方法衍生的烷基阳离子中具有七个或更多碳原子的烷烃的质子分解。位于 δ 处或远离底物中氧代基团的叔 C-H 键可以在 -20°C 下专门反应生成 (ω-1)-氧代-2,2-二甲基羧酸。