1-Methoxy-2-aethyl-pentan | 18668-81-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-Methoxy-2-aethyl-pentan
• 英文别名: 1-Methoxy-2-ethyl-pentan；3-Methoxymethyl-4-chlor-hexen-(3)；3-methoxymethyl-hexane；3-(Methoxymethyl)hexane
• CAS: 18668-81-0
• 化学式: C₈H₁₈O
• 分子量: 130.23
• InChiKey: GQUKVXJDZBIHCV-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：
  5
• 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：

  3-己炔 、 氯甲基甲基醚 生成 1-Methoxy-2-aethyl-pentan
  参考文献：
  名称：

  Turbanova,E.S. et al., Journal of Organic Chemistry USSR (English Translation), 1967, vol. 3, p. 1515 - 1521

  摘要：

  DOI：

文献信息

• BIARYL AMIDE DERIVATIVE OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF
  申请人：Katayama Seiji

  公开号：US20130116227A1

  公开（公告）日：2013-05-09

  Disclosed is a novel biaryl amide derivative represented by formula (1) and having an affinity for the aldosterone receptor; also disclosed is a pharmaceutically acceptable salt thereof. (In the formula, A is any of the groups represented by formula (a); L is —CONH—, etc.; R 1 is a substitutable aminosulfonyl group, etc.; R 2 is a hydrogen atom, etc.; R 3 is a hydrogen atom, etc.; R 4 is a hydrogen atom, a halogen atom, hydroxy group, a substitutable amino group, a substitutable C 1-6 alkoxy group, a substitutable 4- to 7-membered cyclic amino group, etc.; R 5a , R 5b and R 5c are each independently hydrogen atoms, etc.; R 6 is a halogen atom, a cyano group, etc.; R 7 and R 8 are each independently a hydrogen atom, etc.; and m is an integer such as 0.)

  揭示了一种表示为公式（1）的新型联苯酰胺衍生物，具有与醛固酮受体的亲和力；还揭示了其药用可接受的盐。（在该公式中，A是由公式（a）表示的任何基团之一；L是—CONH—等；R1是可替代的氨基磺酰基等；R2是氢原子等；R3是氢原子等；R4是氢原子、卤原子、羟基、可替代的氨基基团、可替代的C1-6烷氧基、可替代的4-到7-成员环氨基基团等；R5a、R5b和R5c各自独立地是氢原子等；R6是卤原子、氰基等；R7和R8各自独立地是氢原子等；m是整数，例如0。）
• Haloalkylmethyleneoxyphenyl-substituted ketoenols
  申请人：Fischer Reiner

  公开号：US20100311593A1

  公开（公告）日：2010-12-09

  The invention relates to novel compounds of the formula (I), in which W, X, Y, Z and CKE are each as defined above, to several methods and intermediates for preparation thereof and to the use thereof as pesticides and/or herbicides. The invention also relates to selective herbicidal compositions which comprise firstly haloalkylmethyleneoxyphenyl-substituted ketoenols and secondly a compound which improves crop plant compatibility. The present invention further relates to the enhancement of the action of crop protection compositions comprising especially haloalkylmethyleneoxyphenyl-substituted ketoenols, by the addition of ammonium or phosphonium salts and optionally penetration enhancers, to the corresponding compositions, to methods for production thereof and to the use thereof in crop protection as insecticides and/or acaricides and/or for preventing undesired plant growth.

  该发明涉及公式（I）中的新化合物，其中W、X、Y、Z和CKE各自如上所定义，以及其制备的几种方法和中间体，以及将其用作杀虫剂和/或除草剂的用途。该发明还涉及选择性除草剂组合物，其首先包括卤代烷基亚甲氧基苯基取代酮烯醇，其次包括改善作物植物相容性的化合物。本发明还涉及通过添加铵盐或磷盐以及必要时的渗透增效剂，增强特别是卤代烷基亚甲氧基苯基取代酮烯醇的作物保护组合物的作用，以及相应组合物的制备方法和将其用于作物保护作为杀虫剂和/或螨虫剂和/或预防不受欢迎的植物生长。
• Triptycene analogs
  申请人：——

  公开号：US20020091163A1

  公开（公告）日：2002-07-11

  This invention provides analogs of triptycene which are useful as anticancer drugs, as well as for other uses. The potency of these compounds is in a similar magnitude as daunomycin, a currently used anticancer drug. Each compound of the invention produces one or more desired effects (blocking nucleoside transport, inhibiting nucleic acid or protein syntheses, decreasing the proliferation and viability of cancer cells, inducing DNA fragmentation or retaining their effectiveness against multidrug-resistant tumor cells).

  这项发明提供了三苯乙烯的类似物，可用作抗癌药物，以及其他用途。这些化合物的效力与目前使用的抗癌药达诺霉素相当。该发明的每种化合物都产生一个或多个期望的效果（阻断核苷酸转运、抑制核酸或蛋白质合成、降低癌细胞的增殖和存活能力、诱导DNA断裂或保持其对多药耐药肿瘤细胞的有效性）。
• Trifluromethoxyphenyl-Substituted Tetramic Acid Derivatives Pesticides and/or Herbicides
  申请人：Fischer Reiner

  公开号：US20120015807A1

  公开（公告）日：2012-01-19

  The present invention relates to novel trifluoromethoxyphenyl-substituted tetramic acid derivatives of the formula (I), in which J, X, Y, A, B, D and G have the meanings given above, to a number of processes for their preparation, and to their use as pesticides and/or herbicides. The invention further provides selective herbicidal compositions which comprise, firstly, trifluoromethoxyphenyl-substituted tetramic acid derivatives and, secondly, a crop plant compatibility-improving compound. The invention further relates to the boosting of the action of crop protection compositions comprising compounds of the formula (I) through the additions of ammonium salts or phosphonium salts and optionally penetrants.

  本发明涉及一种新型的三氟甲氧基苯基取代的四酰胺酸衍生物，其化学式为(I)，其中J、X、Y、A、B、D和G具有上述给定的含义，以及它们的制备方法，以及它们作为杀虫剂和/或除草剂的用途。该发明进一步提供了选择性除草剂组合物，其包括首先为三氟甲氧基苯基取代的四酰胺酸衍生物，其次为一种改善作物植物兼容性的化合物。该发明还涉及通过添加铵盐或磷盐以及可选的渗透剂来增强化合物(I)的作物保护组合物的作用。
• [EN] TRIPTYCENE ANALOGS<br/>[FR] ANALOGUES DE TRIPTYCÈNE
  申请人：UNIV KANSAS STATE

  公开号：WO2002028808A1

  公开（公告）日：2002-04-11

  This invention provides analogs of triptycene which are useful as anticancer drugs, as well as for other uses. The potency of these compounds is in a similar magnitude as daunomycin, a currently used anticancer drug. Each compound of the invention produces one or more desired effects (blocking nucleoside transport, inhibiting nucleic acid or protein syntheses, decreasing the proliferation and viability of cancer cells, inducing DNA fragmentation or retaining their effectiveness against multidrug-resistant tumor cells).

  本发明提供了三苯甲烷的类似物，可用作抗癌药物，以及其他用途。这些化合物的效力与目前使用的抗癌药物多柔比星相似。本发明的每个化合物都产生一个或多个期望的效果（阻止核苷酸转运，抑制核酸或蛋白质合成，减少癌细胞的增殖和生存能力，诱导DNA断裂或保持它们对多药耐药肿瘤细胞的有效性）。