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methyl γ-cyclohexyloxyacetoacetate | 415678-66-9

中文名称
——
中文别名
——
英文名称
methyl γ-cyclohexyloxyacetoacetate
英文别名
4-cyclohexyloxy-3-oxo-butyric acid methyl ester;methyl 4-cyclohexyloxy-3-oxobutanoate
methyl γ-cyclohexyloxyacetoacetate化学式
CAS
415678-66-9
化学式
C11H18O4
mdl
——
分子量
214.262
InChiKey
CXIKBYYPIYCNLR-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:
    318.1±17.0 °C(Predicted)
  • 密度:
    1.07±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    15
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    methyl γ-cyclohexyloxyacetoacetate 在 dirhodium tetraacetate 4-二甲氨基吡啶三乙胺甲烷磺酰基叠氮化物 作用下, 以 二氯甲烷甲苯乙腈 为溶剂, 生成 (Z)-4-[(-)-menthoxycarbonylmethylidene]-2-(pentane-1,5-diyl)-1,3-dioxolane
    参考文献:
    名称:
    Ruthenium(II) Porphyrin Catalyzed Formation of (Z)-4-Alkyloxycarbonyl- methylidene-1,3-dioxolanes from γ-Alkoxy-α-diazo-β-ketoesters
    摘要:
    [GRAPHICS]Ruthenum(II) porphyrins and dirhodium(II) acetate catalyze cyclization of gamma-alkoxy-alpha-diazo-beta-ketoesters to (Z)-4-(alkyloxycarbonylmethylidene)-1,3-dioxolanes selectively (ca. 68% yield) with no formation of 3(2H)-furanones. Reacting a diazo ketoester with [Ru-II(TTP)(CO)] [H2TTP = meso-tetrakis(p-tolyl) porphyrin] in toluene afforded a ruthenium carbenoid complex, which has been isolated and spectroscopically characterized. A mechanism involving hydrogen atom migration from the C-H bond to the ruthenium carbenoid is proposed.
    DOI:
    10.1021/ol010283f
  • 作为产物:
    描述:
    4-溴-3-氧代-丁酸甲酯环己醇 在 sodium hydride 作用下, 以 四氢呋喃正己烷 为溶剂, 以62%的产率得到methyl γ-cyclohexyloxyacetoacetate
    参考文献:
    名称:
    Ruthenium(II) Porphyrin Catalyzed Formation of (Z)-4-Alkyloxycarbonyl- methylidene-1,3-dioxolanes from γ-Alkoxy-α-diazo-β-ketoesters
    摘要:
    [GRAPHICS]Ruthenum(II) porphyrins and dirhodium(II) acetate catalyze cyclization of gamma-alkoxy-alpha-diazo-beta-ketoesters to (Z)-4-(alkyloxycarbonylmethylidene)-1,3-dioxolanes selectively (ca. 68% yield) with no formation of 3(2H)-furanones. Reacting a diazo ketoester with [Ru-II(TTP)(CO)] [H2TTP = meso-tetrakis(p-tolyl) porphyrin] in toluene afforded a ruthenium carbenoid complex, which has been isolated and spectroscopically characterized. A mechanism involving hydrogen atom migration from the C-H bond to the ruthenium carbenoid is proposed.
    DOI:
    10.1021/ol010283f
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文献信息

  • Pyrimidine derivatives as IL-8 receptor antagonists
    申请人:——
    公开号:US20040087601A1
    公开(公告)日:2004-05-06
    Compounds containing the pyrimidine nucleus and their use to treat diseases and conditions related to inappropriate Interleukin-8 receptor activity are disclosed. The compounds are of the formula I 1 In these compounds, Q is preferably unsubstituted and substituted heterocyclyl; U is usually hydrogen or fluorine; and V is preferably hydrogen, halogen, alkyl, —O—alkyl or —S-alkyl. A representative example is: 2
    含有嘧啶核的化合物及其用于治疗与不适当的白细胞介素-8受体活性相关的疾病和症状的用途已被披露。这些化合物的结构式为I 1 在这些化合物中,Q最好是未取代或取代的杂环烷基;U通常是氢或氟;V最好是氢、卤素、烷基、—O—烷基或—S-烷基。一个代表性的例子是: 2
  • US7037916B2
    申请人:——
    公开号:US7037916B2
    公开(公告)日:2006-05-02
  • [EN] PYRIMIDINE DERIVATIVES AS IL-8 RECEPTOR ANTAGONISTS<br/>[FR] DERIVES DE PYRIMIDINE UTILISES COMME ANTAGONISTES DES RECEPTEURS DE L'IL-8
    申请人:PHARMACOPEIA INC
    公开号:WO2004062609A2
    公开(公告)日:2004-07-29
    Compounds containing the pyrimidine nucleus and their use to treat diseases and conditions related to inappropriate Interleukin-8 receptor activity are disclosed. The compounds are of the formula (I). In these compounds, Q is preferably unsubstituted and substituted heterocyclyl; U is usually hydrogen or fluorine; and V is preferably hydrogen, halogen, alkyl, -O-alkyl or -S-alkyl. A representative example is formula (X).
  • Ruthenium(II) Porphyrin Catalyzed Formation of (<i>Z</i>)-4-Alkyloxycarbonyl- methylidene-1,3-dioxolanes from <i>γ</i>-Alkoxy-<i>α</i>-diazo-<i>β</i>-ketoesters
    作者:Shi-Long Zheng、Wing-Yiu Yu、Chi-Ming Che
    DOI:10.1021/ol010283f
    日期:2002.3.1
    [GRAPHICS]Ruthenum(II) porphyrins and dirhodium(II) acetate catalyze cyclization of gamma-alkoxy-alpha-diazo-beta-ketoesters to (Z)-4-(alkyloxycarbonylmethylidene)-1,3-dioxolanes selectively (ca. 68% yield) with no formation of 3(2H)-furanones. Reacting a diazo ketoester with [Ru-II(TTP)(CO)] [H2TTP = meso-tetrakis(p-tolyl) porphyrin] in toluene afforded a ruthenium carbenoid complex, which has been isolated and spectroscopically characterized. A mechanism involving hydrogen atom migration from the C-H bond to the ruthenium carbenoid is proposed.
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