Hydroxy-butyl-cyclohexyl-ether | 1927-72-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: Hydroxy-butyl-cyclohexyl-ether
• 英文别名: 4-Cyclohexyloxy-1-butanol；4-Cyclohexyl-1-butanol；4-Cyclohexyloxybutan-1-ol
• CAS: 1927-72-6
• 化学式: C₁₀H₂₀O₂
• 分子量: 172.268
• InChiKey: SSWUADMZNHHZGV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  12
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  4-phenoxybutan-1-ol 在 platinum(IV) oxide 氢气 作用下， 以 溶剂黄146 为溶剂， 生成 Hydroxy-butyl-cyclohexyl-ether
  参考文献：
  名称：

  Reductions with Metal Hydrides. XIV. Reduction of 2-Tetrahydropyranyl and 2-Tetrahydrofuranyl Ethers

  摘要：

  DOI：

  10.1021/jo01018a082

文献信息

• [EN] THE RING OPENING OF LACTONES AND LACTAMS<br/>[FR] OUVERTURE DE CYCLE DE LACTONES ET DE LACTAMES
  申请人：NOVARTIS AG

  公开号：WO2011019789A1

  公开（公告）日：2011-02-17

  The present invention provides a novel process for opening a lactone and/or a lactam ring. More particularly, the present invention provides a process that employs a novel catalyst in the opening of a lactone ring and/or a lactam ring. Additionally, the present invention also provides a novel deprotection process of any protecting group present in either the lactone ring-containing and/or lactam ring-containing compound and/or in the ring-opened product thereof.

  本发明提供了一种新颖的打开内酯和/或内酰胺环的方法。更具体地说，本发明提供了一种在打开内酯环和/或内酰胺环中使用新型催化剂的方法。此外，本发明还提供了一种新颖的去保护过程，用于去除内含内酯环和/或内酰胺环的化合物中任何保护基，以及去除其环打开产物中的保护基。
• OPTICAL RECORDING MEDIUM AND COMPOUND USED FOR THE SAME
  申请人：SHIOZAKI Hiroyoshi

  公开号：US20090306376A1

  公开（公告）日：2009-12-10

  A compound comprising a ring structure including a ring composed of four carbon atoms and two nitrogen atoms and a substituted or unsubstituted amino group bonded to the ring structure.

  一种化合物，包括一个环结构，其中包括由四个碳原子和两个氮原子组成的环，以及与环结构相结合的取代或未取代的氨基团。
• [EN] ORGANIC COMPOUNDS<br/>[FR] COMPOSÉS ORGANIQUES
  申请人：NOVARTIS AG

  公开号：WO2005051895A1

  公开（公告）日：2005-06-09

  Disclosed are δ-amino-Ϝ-hydroxy-ω-aryl-alkanoic acid amide compounds of formula (I) and the salts thereof, having renin-inhibiting properties. Also disclosed are pharmaceutical compositions comprising these compounds and methods of administering them for the treatment of hypertension, atherosclerosis, unstable coronary syndrome, congestive heart failure, cardiac hypertrophy, cardiac fibrosis, cardiomyopathy postinfarction, unstable coronary syndrome, diastolic dysfunction, chronic kidney disease, hepatic fibrosis, complications resulting from diabetes, such as nephropathy, vasculopathy and neuropathy, diseases of the coronary vessels, restenosis following angioplasty, raised intra-ocular pressure, glaucoma, abnormal vascular growth, hyperaldosteronism, cognitive impairment, alzheimers, dementia, anxiety states and cognitive disorders.

  揭示了具有抑制肾素作用的δ-氨基-Ϝ-羟基-ω-芳基-烷酸酰胺化合物的化学式(I)及其盐。还揭示了包含这些化合物的药物组合物以及用于治疗高血压、动脉粥样硬化、不稳定性冠状动脉综合征、充血性心力衰竭、心肌肥大、心脏纤维化、心肌病后梗死、不稳定性冠状动脉综合征、舒张功能障碍、慢性肾脏疾病、肝纤维化、糖尿病引起的并发症（如肾病、血管病和神经病变）、冠状动脉疾病、血管成形术后再狭窄、眼内压升高、青光眼、异常血管生长、高醛固酮症、认知障碍、阿尔茨海默病、痴呆、焦虑状态和认知障碍的治疗方法。
• CHEMOSELECTIVE REDUCTIVE CLEAVAGE OF KETALS AND ACETALS
  作者：R. J. Borders、T. A. Bryson

  DOI：10.1246/cl.1984.9

  日期：1984.1.5

  Utilization of complexed monochloroborane as a reducing agent for ketals and acetals is reported.

  报道了使用络合的一氯硼烷作为缩酮和缩醛的还原剂。
• Methods of treating alzheimer's disease using aryl alkanoic acid amides
  申请人：John Varghese

  公开号：US20060154926A1

  公开（公告）日：2006-07-13

  Disclosed are methods for treating Alzheimer's disease, and other diseases, and/or inhibiting beta-secretase enzyme, and/or inhibiting deposition of A beta peptide in a mammal, by use of compounds of formula (1) wherein the variables R 1 -R 8 and X are defined herein.

  本发明涉及使用式（1）中所述的化合物治疗阿尔茨海默病和其他疾病，抑制β-分泌酶酶活性和/或抑制Aβ肽在哺乳动物体内的沉积的方法，其中变量R1-R8和X在此定义。