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3-acetyl-9,10-dimethoxyphenanthrene | 897649-08-0

中文名称
——
中文别名
——
英文名称
3-acetyl-9,10-dimethoxyphenanthrene
英文别名
1-(9,10-Dimethoxyphenanthren-3-yl)ethanone
3-acetyl-9,10-dimethoxyphenanthrene化学式
CAS
897649-08-0
化学式
C18H16O3
mdl
——
分子量
280.323
InChiKey
BUNVAXIAOSTHHD-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

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

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

  • 作为反应物:
    描述:
    3-acetyl-9,10-dimethoxyphenanthrene4-二甲氨基吡啶 、 sodium dithionite 、 三乙胺 作用下, 以 二氯甲烷乙酸乙酯1,2-二氯乙烷甲苯 为溶剂, 反应 30.67h, 生成 4,7,7-trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid 1,2,5,7-tetramethoxy-dibenzo[c,g]phenanthren-10-yl ester
    参考文献:
    名称:
    A [5]HELOL Analogue That Senses Remote Chirality in Alcohols, Phenols, Amines, and Carboxylic Acids
    摘要:
    A route is developed to a structural analogue of [5]HELOL, a previously reported helically grooved sensor of remote chirality. It gives the material enantiomerically pure and in multigram quantities. The enantiomers of alcohols, phenols, amines, and carboxylic acids, even when their centers of chirality are remote from any functional groups, can be differentiated by P-31 NMR spectroscopic analyses of their reaction products with the chlorophosphite of this material.
    DOI:
    10.1021/jo0512913
  • 作为产物:
    描述:
    9,10-dimethoxyphenanthrene乙酰氯三氯化铝 作用下, 以 二氯甲烷 为溶剂, 以28.2 g的产率得到3-acetyl-9,10-dimethoxyphenanthrene
    参考文献:
    名称:
    A [5]HELOL Analogue That Senses Remote Chirality in Alcohols, Phenols, Amines, and Carboxylic Acids
    摘要:
    A route is developed to a structural analogue of [5]HELOL, a previously reported helically grooved sensor of remote chirality. It gives the material enantiomerically pure and in multigram quantities. The enantiomers of alcohols, phenols, amines, and carboxylic acids, even when their centers of chirality are remote from any functional groups, can be differentiated by P-31 NMR spectroscopic analyses of their reaction products with the chlorophosphite of this material.
    DOI:
    10.1021/jo0512913
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文献信息

  • Continuous flow photocyclization of stilbenes – scalable synthesis of functionalized phenanthrenes and helicenes
    作者:Quentin Lefebvre、Marc Jentsch、Magnus Rueping
    DOI:10.3762/bjoc.9.221
    日期:——
    A continuous flow oxidative photocyclization of stilbene derivatives has been developed which allows the scalable synthesis of backbone functionalized phenanthrenes and helicenes of various sizes in good yields.
    已经开发了二苯乙烯衍生物的连续流动氧化光环化,它允许以良好的产率大规模合成各种尺寸的骨架官能化菲和螺旋。
  • Substituted phenanthrene diketo acids and uses therefor
    申请人:Buolamwini John K.
    公开号:US20090088444A1
    公开(公告)日:2009-04-02
    Provided herein are substituted phenanthrene diketo acid compounds. These compounds comprise the diketo acid moiety on one of carbons C1-C4 and C9 in the phenanthrene ring and at least one further substitutent on the other ring carbons. Also provided are methods of inhibiting an activity of a human immunodeficiency virus (HIV) integrase protein and treating an HIV infection in a subject using the substituted phenanthrene diketo acid compounds.
  • A [5]HELOL Analogue That Senses Remote Chirality in Alcohols, Phenols, Amines, and Carboxylic Acids
    作者:David Zhigang Wang、Thomas J. Katz
    DOI:10.1021/jo0512913
    日期:2005.10.1
    A route is developed to a structural analogue of [5]HELOL, a previously reported helically grooved sensor of remote chirality. It gives the material enantiomerically pure and in multigram quantities. The enantiomers of alcohols, phenols, amines, and carboxylic acids, even when their centers of chirality are remote from any functional groups, can be differentiated by P-31 NMR spectroscopic analyses of their reaction products with the chlorophosphite of this material.
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