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8-hydroxy-1H-isochromen-1-one | 4702-36-7

中文名称
——
中文别名
——
英文名称
8-hydroxy-1H-isochromen-1-one
英文别名
8-hydroxyisochromen-1-one
8-hydroxy-1H-isochromen-1-one化学式
CAS
4702-36-7
化学式
C9H6O3
mdl
——
分子量
162.145
InChiKey
GZFXAOPNTDYZLP-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:
    342.7±42.0 °C(Predicted)
  • 密度:
    1.403±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:e570deb81dd2328fb5e35598a352dbe0
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反应信息

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文献信息

  • Concise Synthesis of Isocoumarins through Rh-Catalyzed Direct Vinylene Annulation: Scope and Mechanistic Insight
    作者:Gen Mihara、Koushik Ghosh、Yuji Nishii、Masahiro Miura
    DOI:10.1021/acs.orglett.0c02112
    日期:2020.7.17
    subsequent C–C bond formation have emerged as powerful synthetic tools for the synthesis of elaborate cyclic molecules. In this report, we introduce an efficient synthetic method of 3,4-unsubstituted isocoumarins adopting an electron-deficient CpERh complex as the catalyst. The use of vinylene carbonate as a vinylene transfer reagent enables the direct construction of isocoumarins from readily available
    惰性C–H键的过渡金属催化活化和随后的C–C键形成已成为合成精细环状分子的有力合成工具。在本报告中,我们介绍了一种有效的合成方法,该方法采用缺电子的Cp E Rh络合物作为催化剂来合成3,4-未取代的异香豆素。碳酸亚乙烯酯作为亚乙烯基转移试剂的使用使得可以从容易获得的苯甲酸直接构建异香豆素,而无需任何外部氧化剂和碱。通过计算分析评估反应机理,以发现催化循环内前所未有的“铑转移”事件。
  • JPH05317396A
    申请人:——
    公开号:JPH05317396A
    公开(公告)日:1993-12-03
  • JPS58162586A
    申请人:——
    公开号:JPS58162586A
    公开(公告)日:1983-09-27
  • Novel Quinoline Compound, and Composition Containing Centipede Extract or Compounds Isolated Therefrom for Prevention and Treatment of Cardiovascular Disease
    申请人:Park Ho Yong
    公开号:US20090247758A1
    公开(公告)日:2009-10-01
    The present invention relates to a composition for the prevention and treatment of cardiovascular diseases containing the novel quinoline compound, the centipede extracts or compounds isolated from the extracts. The novel quinoline compound, the centipede extracts or a quinoline compound and a phenol compound isolated from the extracts of the invention exhibit excellent LDL-antioxidant activity, ACAT inhibiting activity, and anti-inflammatory activities, so that they can be included as an effective ingredient in a composition for the prevention and treatment of cardiovascular disease including hyperlipidemia, atherosclerosis, coronary heart disease, and myocardial infarction mediated by LDL-oxidation, cholesteryl ester synthesis and accumulation, and inflammation.
  • NOVEL QUINOLINE COMPOUND, AND COMPOSITION CONTAINING CENTIPEDE EXTRACT OR COMPOUNDS ISOLATED THEREFROM FOR PREVENTION AND TREATMENT OF CARDIOVASCULAR DISEASE
    申请人:PARK Ho Yong
    公开号:US20120220626A1
    公开(公告)日:2012-08-30
    The present invention relates to a composition for the prevention and treatment of cardiovascular diseases containing the novel quinoline compound, the centipede extracts or compounds isolated from the extracts. The novel quinoline compound, the centipede extracts or a quinoline compound and a phenol compound isolated from the extracts of the invention exhibit excellent LDL-antioxidant activity, ACAT inhibiting activity, and anti-inflammatory activities, so that they can be included as an effective ingredient in a composition for the prevention and treatment of cardiovascular disease including hyperlipidemia, atherosclerosis, coronary heart disease, and myocardial infarction mediated by LDL-oxidation, cholesteryl ester synthesis and accumulation, and inflammation.
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同类化合物

锡(4+)丙烯酰酸酯 茵陈蒿素 苯并噻吨二羧酸酐 苯并[d]茚并[1,2-b]吡喃-5,11-二酮 苯并[E][2]苯并吡喃并[4,3-b]吲哚-5(13H)-酮 腐皮壳菌素 脱乙酰基杜克拉青霉素 网状菌醇 短叶苏木酚酸甲酯 氨甲酸,(4-氯-3-甲氧基-1-羰基-1H-2-苯并吡喃-7-基)-,乙基酯 异薰草素 培黄素 四(4-甲酰基苯基)硅烷 [2]苯并吡喃并[3',4':4,5]吡咯并[2,3-f]异喹啉-8(13H)-酮 N,N-二甲基-1-氧代-4-苯基-1H-2-苯并吡喃-3-甲酰胺 8-羟基-6-甲氧基-3-丙基异香豆素 8-羟基-4-(2-羟基乙酰基)异苯并吡喃-1-酮 8-羟基-3-(羟基甲基)-6-甲氧基异苯并吡喃-1-酮 8-羟基-3-(4-羟基苯基)异色烯-1-酮 8-羟基-3,4-二甲基-1H-2-苯并吡喃-1-酮 8-甲氧基-3-甲基-1H-异苯并吡喃-1-酮 7-氨基-4-氯-3-甲氧基异香豆素 7-氨基-4-氯-3-(3-异硫脲基丙氧基)异香豆素 7-氨基-4-氯-3-(2-甲氧基乙氧基)异色烯-1-酮 7-氨基-3-(2-溴乙氧基)异色烯-1-酮 7-氨基-3-(2-溴乙氧基)-4-氯异苯并吡喃-1-酮 7,8,9-三羟基-3,5-二氧代-1,2-二氢环戊烯并[c]异苯并吡喃-1-羧酸乙酯 6-甲氧基-1H-2-苯并吡喃-1-酮 6-氟-3-甲氧基-1-氧代-1H-2-苯并吡喃-4-甲酸甲酯 6,8-二羟基-3-(羟甲基)异色烯-1-酮 5-羟基-7-苯基-1H,6H-苯并[de]异苯并吡喃-1,6-二酮 5-硝基-1H-异色烯-1-酮 5-溴-1H-异苯并吡喃-1-酮 5,7-二甲氧基-4-苯基-异色烯-1-酮 5,6-二氢-1H,4H-萘并[1,8-cd]吡喃-1-酮 4-甲氧基-7-甲基吡喃并[3,4-f][1]苯并呋喃-5-酮 4-氰基-3-苯基异香豆素 4-氯-3-乙氧基-7-胍基异香豆素 4-乙酰基异苯并吡喃-1-酮 4-(哌啶-1-羰基)异色烯-1-酮 3-甲基异色烯-1-酮 3-甲基-6-甲氧基-8-羟基异香豆素 3-甲基-1-氧代-1H-异苯并吡喃-4-甲酸 3-氨基-4-(3-甲基苯胺基)异色烯-1-酮 3-乙酰氧基甲基异香豆素 3-乙基-异色烯-1-酮 3-[3,5-二甲基-4-(2-(4-甲基哌嗪-1-基)-乙氧基)-苯基]-6,8-二甲氧基-异色烯-1-酮 3-[(2-氯苯基)甲基]异色烯-1-酮 3-(4'-氯-2'-氟苯基)异香豆素 3-(3,4-二羟基苯基)-8-羟基异苯并吡喃-1-酮