摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-ethyl-1-hexanol | 66576-32-7

中文名称
——
中文别名
——
英文名称
4-ethyl-1-hexanol
英文别名
4-ethylhexan-1-ol
4-ethyl-1-hexanol化学式
CAS
66576-32-7
化学式
C8H18O
mdl
——
分子量
130.23
InChiKey
RLGDVTUGYZAYIX-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    96 °C(Press: 20 Torr)
  • 密度:
    0.821±0.06 g/cm3(Predicted)

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:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:99ff05f7083ca2af829758e87039a3e8
查看

反应信息

  • 作为反应物:
    描述:
    4-ethyl-1-hexanolpotassium carbonate三乙胺 、 potassium iodide 作用下, 以 乙酸乙酯乙腈 为溶剂, 生成
    参考文献:
    名称:
    J-104129, a novel muscarinic M3 receptor antagonist with high selectivity for M3 over M2 receptors
    摘要:
    A new class of 4-acetamidopiperidine derivatives has been synthesized and investigated for human muscarinic receptor subtype selectivity. Introduction of a hydrocarbon chain of appropriate length into the piperidine nitrogen of the racemic N-(piperidin-4-yl)-2-cyclobutyl-2-hydroxy-2-phenylacetamide platform conferred up to 70-fold selectivity for human muscarinic M-3 receptors over M-2 receptors. Subsequent synthetic derivatizations resulted in highly potent M-3 receptor antagonists with selectivity greater than two orders of magnitude for M-3 over M-2 receptors, from which the analogue 4r was selected. Preparation of both enantiomers of 4r led to the identification of (2R)-N-[1-(4-methyl-3-pentenyl)piperidin-4-yl]-2-cyclopentyl-2-hydroxy-2-phenylacetamide (J-104129, (R)-4r), which exhibited 120-fold selectivity for Mg receptors (K-i = 4.2 nM) over M-2 receptors (K-i = 490 nM). In isolated rat trachea, (R)-4r potently and specifically antagonized acetylcholine (ACh)-induced responses with a K-B value of 3.3 nM. The highly subtype-selective profile was also seen in isolated rat tissue assays (50-fold) and in anesthetized rats (> 250-fold). Oral administration of J-104129 ((R)-4r) antagonized ACh-induced bronchoconstriction with an ED50 value of 0.58 mg/kg in rats. Thus, J-104129 ((R)-4r) may effectively facilitate bronchodilation in the treatment of obstructive airway disease. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(99)00177-7
  • 作为产物:
    描述:
    环氧乙烷 、 alkaline earth salt of/the/ methylsulfuric acid 生成 4-ethyl-1-hexanol
    参考文献:
    名称:
    Prout; Cason, Journal of Organic Chemistry, 1949, vol. 14, p. 134
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Dual Rh−Ru Catalysts for Reductive Hydroformylation of Olefins to Alcohols
    作者:Fábio M. S. Rodrigues、Peter K. Kucmierczyk、Marta Pineiro、Ralf Jackstell、Robert Franke、Mariette M. Pereira、Matthias Beller
    DOI:10.1002/cssc.201800488
    日期:2018.7.20
    described. Apart from terminal, di‐ and trisubstituted olefins, for the first time the less active internal C−C double bond of tetrasubstituted alkenes can also be utilized. As an example, 2,3‐dimethylbut‐2‐ene is converted into the corresponding n‐alcohol with high yield (90 %) as well as regio‐ and chemoselectivity (>97 %). Key for this development is the use of a combination of Rh complexes with bulky
    描述了一种促进多米诺加氢甲酰化-还原反应的主动选择性双催化体系。除了末端取代的二,三取代烯烃外,还第一次可以使用四取代烯烃的活性较低的内部CC双键。例如,将2,3-二甲基丁-2-烯转化为相应的正丙醇,产率高(90%),区域和化学选择性(> 97%)。该开发的关键是将Rh配合物与庞大的单亚磷酸酯配体和Ru基Shvo配合物结合使用。可以直接使用多种芳族和脂族烯烃来获得主要为线性的醇。
  • 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] PROCESS<br/>[FR] PROCÉDÉ
    申请人:PHOSPHAGENICS LTD
    公开号:WO2018112512A1
    公开(公告)日:2018-06-28
    An efficient and commercial phosphorylation process of a complex alcohol, such as secondary and tertiary alcohols, with P4O10 at high temperatures, and a product obtained by the process.
    一种高效商业化的磷酸酯化过程,用于复杂醇类(如二级和三级醇),在高温下使用P4O10,以及该过程得到的产品。
  • FULLERENE DERIVATIVE AND n-TYPE SEMICONDUCTOR MATERIAL
    申请人:DAIKIN INDUSTRIES, LTD.
    公开号:US20180282274A1
    公开(公告)日:2018-10-04
    An object of the present invention is to provide a novel fullerene derivative usable in n-type semiconductor materials for organic thin-film solar cells and the like. The object is achieved by a fullerene derivative represented by formula (1) wherein R 1 represents aryl optionally substituted with at least one substituent, R 2 represents an organic group, R 3 represents an organic group, with the proviso that at least one of R 2 and R 3 is alkyl optionally substituted with at least one substituent or alkyl ether optionally substituted with at least one substituent, R 4 represents hydrogen or an organic group, and a ring A represents a fullerene ring.
    本发明的目的是提供一种新型富勒烯衍生物,可用于有机薄膜太阳能电池等n型半导体材料。该目的通过由式(1)表示的富勒烯衍生物实现,其中R1代表芳基,可选择地取代至少一个取代基,R2代表有机基团,R3代表有机基团,但至少R2和R3中的一个是烷基,可选择地取代至少一个取代基或烷基醚,可选择地取代至少一个取代基,R4代表氢或有机基团,环A代表一个富勒烯环。
  • [EN] STERICALLY HINDERED AMINE STABILIZER<br/>[FR] AGENT STABILISANT AMINÉ STÉRIQUEMENT ENCOMBRÉ
    申请人:BASF SE
    公开号:WO2011029744A1
    公开(公告)日:2011-03-17
    The present invention relates to oxygen-substituted sterically hindered amines of the formulae I or II: (II), wherein, for example, F2, R3, R5, R6, R8, R9, R11, R12, R13, R14 are n-butyl; Z1 to Z10 are propoxy and R1, R4, R7, R10, R13 are 2,2,6,6-tetramethyl-1 -propoxy-piperidin-4-yl. Compositions comprising compounds of formulae I or Il and an organic material, which is susceptible to oxidative, thermal or light- induced degradation, are further disclosed. Optionally, further additives are contained.
    本发明涉及具有以下式I或II的含氧受位阻胺类化合物:(II),其中,例如,F2、R3、R5、R6、R8、R9、R11、R12、R13、R14为正丁基;Z1至Z10为丙氧基,R1、R4、R7、R10、R13为2,2,6,6-四甲基-1-丙氧基-哌啶-4-基。还公开了包含具有式I或II的化合物和易于氧化、热降解或光诱导降解的有机材料的组合物。可选地,还包含进一步添加剂。
查看更多