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4-(丙基氧基)环己酮 | 158836-67-0

中文名称
4-(丙基氧基)环己酮
中文别名
——
英文名称
4-(propyloxy)cyclohexanone
英文别名
4-propoxycyclohexanone;4-propoxycyclohexan-1-one
4-(丙基氧基)环己酮化学式
CAS
158836-67-0
化学式
C9H16O2
mdl
——
分子量
156.225
InChiKey
XHLFNRDYLLAEEV-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:
    228.9±33.0 °C(Predicted)
  • 密度:
    0.95±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2914509090

SDS

SDS:71097035a6a61f877948f57a18de3d1e
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • NOVEL COMPOUNDS-300
    申请人:Cheng Yun-Xing
    公开号:US20090275574A1
    公开(公告)日:2009-11-05
    Compounds of Formula I, or pharmaceutically acceptable salts thereof: wherein R 1 , R 2 , R 3 , R 4 , m, n, q, s, t, X, and Y are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.
    式I的化合物,或其药用盐:其中R1、R2、R3、R4、m、n、q、s、t、X和Y的定义如规范中所述,以及包括这些化合物的盐和药物组合物已经准备好。它们在治疗中很有用,特别是在疼痛管理中。
  • PREPARATION PROCESS OF PERFLUOROALKYL COMPOUND WITH MONOHYDROPERFLUOROALKANE AS STARTING MATERIAL
    申请人:KANTO DENKA KOGYO CO., LTD.
    公开号:US20190169107A1
    公开(公告)日:2019-06-06
    A simple production process is provided of a perfluoroalkyl compound that uses monohydroperfluoroalkane as a starting material, the perfluoroalkyl compound being an important intermediate of organic electronic materials, medicine, agricultural chemicals, functional polymer materials and the like. With monohydroperfluoroalkane is reacted a base and then a carbonyl compound to produce an alcohol having a perfluoroalkyl group. For example, potassium hydroxide is made to interact with trifluoromethane, and a reaction with a carbonyl compound is induced to produce an alcohol having a trifluoromethyl group.
    提供了一种简单的生产过程,使用单羟基全氟烷作为起始物质来制备全氟烷基化合物,该全氟烷基化合物是有机电子材料、药物、农药、功能性聚合物材料等的重要中间体。使用单羟基全氟烷与碱反应,再与羰基化合物反应,可以产生具有全氟烷基的醇。例如,可以将氢氧化钾与三氟甲烷相互作用,并诱导与羰基化合物反应,以产生具有三氟甲基基团的醇。
  • Hydroxynitrile lyase-catalyzed addition of HCN to 4-substituted cyclohexanones: stereoselective preparation of tetronic acids
    作者:Franz Effenberger、Jürgen Roos、Christoph Kobler、Holger Bühler
    DOI:10.1139/v02-087
    日期:2002.6.1

    The addition of HCN to 4-alkylcyclohexanones 1 to give cyanohydrins 2 is strongly catalyzed by hydroxy-ni trile lyases (HNLs). With PaHNL, from bitter almond, trans-addition occurs almost exclusively, yielding trans-2. With MeHNL, from cassava, cis-addition is preferred to give cis-2. cis-Selectivity is nearly quantitative, especially for cyclohexanones with larger 4-substituents. Comparable results with respect to the stereoselectivity were observed in the HNL-catalyzed addition of HCN to 4-alkoxycyclohexanones 3a–g. In contrast, the stereoselectivity in the HNL-catalyzed addition to 4-alkanoyloxycyclohexanones 3h–k is very poor. The transformation of cis-4-propylcyclohexanone cyanohydrin (2c) into the corresponding cis-spirotetronic acid 7 occurs without any isomerization.Key words: enzyme, hydroxynitrile lyase, cyclohexanones, cyanohydrins, cis/trans-stereoselectivity.

    在4-烷基环己酮1中加入HCN生成腈醇2,这个反应会受到羟基腈酰酶(HNLs)的强烈催化。使用来自苦杏仁的PaHNL,反应主要发生顺式加成,生成顺-2。使用来自木薯的MeHNL,顺式加成优先生成顺-2。对于4-取代基较大的环己酮,顺式选择性几乎是定量的。在HNL催化下,HCN加成到4-烷氧基环己酮3a-g中时,立体选择性的结果与前者相当。相反,在HNL催化下,HCN加成到4-烷酰氧基环己酮3h-k中时,立体选择性非常差。将顺-4-丙基环己酮腈醇(2c)转化为相应的顺-螺四氢酸7时,不会发生任何异构化。关键词:酶、羟基腈酰酶、环己酮、腈醇、顺/反-立体选择性。
  • BENZIMIDAZOLES WHICH HAVE ACTIVITY AT M1 RECEPTOR AND THEIR USES IN MEDICINE
    申请人:COOPER David Gwyn
    公开号:US20120041027A1
    公开(公告)日:2012-02-16
    Compounds of formula (I) and salts and solvates are provided: wherein Uses of the compounds for therapy, for example in the treatment of psychotic disorders and cognitive impairment, are also disclosed.
    提供公式(I)的化合物、盐和溶剂化合物,其中公式(I)如下: 该化合物可用于治疗精神失常和认知障碍等疾病。
  • Compounds which have activity at M1 receptor and their uses in medicine
    申请人:COOPER David Gwyn
    公开号:US20120309789A1
    公开(公告)日:2012-12-06
    Compounds of general formula and their use in the treatment of psychotic disorders and cognitive impairment, are disclosed.
    揭示了一般式化合物及其在治疗精神障碍和认知障碍方面的用途。
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