n-Propyl-neopentyl-aether | 17348-61-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: n-Propyl-neopentyl-aether
• 英文别名: 2,2-dimethyl-1-propoxy-propane；2,2-Dimethyl-1-propoxypropane
• CAS: 17348-61-7
• 化学式: C₈H₁₈O
• 分子量: 130.23
• InChiKey: ZNPQDAPRCXWWCR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  9
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  新戊醇 、 1-碘代丙烷 生成 n-Propyl-neopentyl-aether
  参考文献：
  名称：

  Brune,A.; Schulte,D., Chemische Berichte, 1967, vol. 100, p. 3438 - 3449

  摘要：

  DOI：

文献信息

• NOVEL NAPHTHYRIDINONE DERIVATIVES AND THEIR USE IN THE TREATMENT OF ARRHYTHMIA
  申请人：NOVARTIS AG

  公开号：US20180111932A1

  公开（公告）日：2018-04-26

  The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof; Wherein R 1 , R 3 -R 6 , X 2 and X 3 are as defined herein, a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

  本发明提供了化合物(I)或其药学上可接受的盐；其中R1、R3-R6、X2和X3如本文所定义，一种制造本发明化合物的方法，以及其治疗用途。本发明还提供了药理活性剂的组合和药物组成。
• PEPTIDE NUCLEIC ACID DERIVATIVES WITH GOOD CELL PENETRATION AND STRONG AFFINITY FOR NUCLEIC ACID
  申请人：Lee Jong-Ook

  公开号：US20110178031A1

  公开（公告）日：2011-07-21

  The present invention provides a novel class of peptide nucleic acid derivatives, which show good cell penetration and strong binding affinity for nucleic acid.

  本发明提供了一类新型的肽核酸衍生物，它们具有良好的细胞穿透性和对核酸的强结合亲和力。
• Vitamin D Receptor Modulators
  申请人：Bunel Emilio Enrique

  公开号：US20090018058A1

  公开（公告）日：2009-01-15

  The present invention relates to novel, non-secosteroidal, diaryl compounds with vitamin D receptor (VDR) modulating and psoriasis.

  本发明涉及一种新型的非类固醇二芳基化合物，具有维生素D受体（VDR）调节和治疗牛皮癣的作用。
• VITAMIN D RECEPTOR MODULATORS
  申请人：Bunel Emilio Enrique

  公开号：US20090227604A1

  公开（公告）日：2009-09-10

  The present invention relates to novel, non-secosteroidal, diaryl compounds with vitamin D receptor (VDR) modulating activity that are less hypercalcemic than 1a,25 dihydroxy vitamin D3. These compounds are useful for treating bone disease and psoriasis.

  本发明涉及一种新的、非次级甾体、二芳基化合物，具有维生素D受体（VDR）调节活性，比1a,25二羟基维生素D3的高钙血症更少。这些化合物对治疗骨病和牛皮癣有用。
• COMPOUNDS EXHIBITING THROMBOPOIETIN RECEPTOR AGONISM
  申请人：Takayama Masami

  公开号：US20090318513A1

  公开（公告）日：2009-12-24

  A compound represented by the general formula (I): wherein R 1 is a hydrogen atom, a halogen atom, or the like; R 2 , R 3 , and R 4 are each independently a hydrogen atom, a halogen atom, C1-C15 alkyl optionally substituted with one or more C1-C12 alkyloxy or the like, or the like; R 5 is a hydrogen atom or the like; R 6 and R 7 are a hydrogen atom or the like; R 8 is C1-C3 alkyl or the like; R 9 is a hydrogen atom or the like), a prodrug, a pharmaceutically acceptable salt, or solvate thereof.

  一种由通式（I）表示的化合物：其中R1是氢原子、卤素原子或类似物；R2、R3和R4各自独立地是氢原子、卤素原子、C1-C15烷基（可选地用一个或多个C1-C12烷氧基或类似物取代）或类似物；R5是氢原子或类似物；R6和R7是氢原子或类似物；R8是C1-C3烷基或类似物；R9是氢原子或类似物。该化合物为一种前药、药物可接受的盐或其溶剂。