methyl hexyl sulfone | 89851-52-5

• 分子结构分类: 有机化合物 - 有机硫化合物 - 磺酰类
• 英文名称: methyl hexyl sulfone
• 英文别名: 1-methanesulfonyl-hexane；Hexyl-methyl-sulfon；1-methylsulfonylhexane
• CAS: 89851-52-5
• 化学式: C₇H₁₆O₂S
• 分子量: 164.269
• InChiKey: LJVSNIJYLPTONM-UHFFFAOYSA-N

物化性质

• 熔点：
  48.5 °C
• 沸点：
  90-94 °C(Press: 0.1 Torr)
• 密度：
  0.994±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  10
• 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：
  42.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  methyl hexyl sulfone 以20%的产率得到
  参考文献：
  名称：

  TROYANSKIJ, EH. I.;LAZAREVA, M. I.;DEMCHUK, D. V.;NIKISHIN, G. I., IZV. AN CCCP. CEP. XIM.,(1988) N 9, S. 2138-2144

  摘要：

  DOI：
• 作为产物：
  描述：

  1-(甲硫基)己烷 在 双氧水 作用下， 以 溶剂黄146 为溶剂， 反应 3.0h， 生成 methyl hexyl sulfone
  参考文献：
  名称：

  Polar control in the remote oxidative functionalization of sulfones

  摘要：

  DOI：

  10.1007/bf00962514

文献信息

• PYRAZOLE COMPOUND AND PHARMACEUTICAL USE THEREOF
  申请人：MIURA Tomoya

  公开号：US20130085132A1

  公开（公告）日：2013-04-04

  The present invention provides a pyrazole compound of the following general Formula [Ib] having SGLT1 inhibitory activity, or a pharmaceutically acceptable salt thereof, a pharmaceutical composition comprising the same, and its pharmaceutical use: wherein each symbol is the same as defined in the description.

  本发明提供了一种具有SGLT1抑制活性的下式[Ib]所示的吡唑化合物、或其药物可接受的盐、包含该化合物的药物组合物及其医药用途： 其中每个符号如说明书中所定义。
• IMIDE DERIVATIVE AND FUNGICIDE CONTAINING SAID DERIVATIVE AS ACTIVE INGREDIENT
  申请人：HOKKO CHEMICAL INDUSTRY CO., LTD.

  公开号：US20210007356A1

  公开（公告）日：2021-01-14

  The present invention provides an imide derivative represented by the following formula (1): wherein R 1 is substituted by a substituent such as an isothiazolyl group, Q is substituted by a substituent such as a thiophenyl group, and A is substituted by a substituent such as a pyrazolyl group, and an agricultural and horticultural fungicide offering an excellent fungicidal effect in agricultural and horticultural situations, which is characterized by containing the imide derivative as an active ingredient.

  本发明提供了一种由以下式（1）表示的酰亚胺衍生物： 其中R1被取代为诸如异噻唑基的取代基，Q被取代为诸如噻吩基的取代基，A被取代为诸如吡唑基的取代基，以及一种在农业和园艺情况下提供出色杀菌效果的农业和园艺杀菌剂，其特征在于包含酰亚胺衍生物作为活性成分。
• PYRAZOLE-3-CARBOXYLIC ACID AMIDE DERIVATIVE AND PEST CONTROL AGENT
  申请人：KUMIAI CHEMICAL INDUSTRY CO., LTD.

  公开号：US20200199096A1

  公开（公告）日：2020-06-25

  Embodiments provide a harmful organism control agent containing a pyrazole-3-carboxylic acid amide derivative or a salt thereof as an active ingredient, having an excellent harmful organism controlling effect. A pyrazole-3-carboxylic acid amide derivative represented by general formula [I]: (wherein, R 1 , R 2 , R 3 , R 4 , and R 5 represent a hydrogen atom, halogen atom, C 1 -C 6 alkyl group or the like, R 6 represents a C 1 -C 12 alkyl group, C 1 -C 12 haloalkyl group or the like, R 7 and R 8 represent a hydrogen atom, C 1 -C 12 alkyl group or the like) or an agriculturally acceptable salt thereof, and a harmful organism control agent containing the pyrazole-3-carboxylic acid amide derivative or an agriculturally acceptable salt thereof as an active ingredient.

  实施例提供了一种含有吡唑-3-羧酸酰胺衍生物或其盐作为活性成分的有害生物控制剂，具有出色的有害生物控制效果。一种由通式[I]表示的吡唑-3-羧酸酰胺衍生物：（其中，R1、R2、R3、R4和R5代表氢原子、卤原子、C1-C6烷基或类似物，R6代表C1-C12烷基、C1-C12卤代烷基或类似物，R7和R8代表氢原子、C1-C12烷基或类似物）或其农业可接受的盐，以及一种含有吡唑-3-羧酸酰胺衍生物或其农业可接受的盐作为活性成分的有害生物控制剂。
• [EN] 2-(N-SUBSTITUTED PIPERAZINYL) STEROID DERIVATIVES<br/>[FR] DÉRIVÉS DE STÉROÏDES DE TYPE 2-(PIPÉRAZINYLE N-SUBSTITUÉ)
  申请人：UNIV LAVAL

  公开号：WO2010060215A1

  公开（公告）日：2010-06-03

  Novel chemical agents of Formula I are described herein. More specifically, 2-(N-substituted piperazinyl) pregnane and 2-(N-substituted piperazinyl) androstane derivatives exhibiting cytotoxicity on a variety of cancer cell lines are disclosed herein. (I)

  本文描述了化学式I的新型化学试剂。更具体地，本文披露了对多种癌细胞系表现出细胞毒性的2-(N-取代哌嗪基)孕酮和2-(N-取代哌嗪基)雄烷衍生物。 (I)
• Selective preventives/remedies for progressive lesions after organ damage
  申请人：——

  公开号：US20030181506A1

  公开（公告）日：2003-09-25

  An object of the present invention is to provide a pharmaceutical agents for preventing and/or treating the progressive lesion after the organic damage without inhibiting organic function or regeneration function thereof, by selectively suppressing the induction of cytotoxic effector macrophages which are induced into the damaged organs in response to chemokines and cytokines which are expressed depending on the type of damaged organic tissues.

  本发明的目的是提供一种药物制剂，用于在有机损伤后预防和/或治疗渐进性病变，而不抑制有机功能或再生功能，通过选择性抑制细胞毒性效应巨噬细胞的诱导，这些巨噬细胞是在损伤的器官中受化学因子和细胞因子诱导而表达的，这些化学因子和细胞因子取决于损伤的有机组织的类型。