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6-iodo-2-methylquinazoline | 929193-11-3

中文名称
——
中文别名
——
英文名称
6-iodo-2-methylquinazoline
英文别名
——
6-iodo-2-methylquinazoline化学式
CAS
929193-11-3
化学式
C9H7IN2
mdl
——
分子量
270.072
InChiKey
BPAQAPRVFPJRFE-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):
    2.6
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    25.8
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • Bicyclic aromatic substituted pyridone derivative
    申请人:Sakuraba Shunji
    公开号:US20090264426A1
    公开(公告)日:2009-10-22
    Disclosed is a compound represented by the formula (I): Wherein R 1 and R 2 independently represent a hydrogen atom, a lower alkyl group or the like; X 1 , X 2 and X 3 independently represent a methine group or a nitrogen atom; Y 1 and Y 3 independently represent a single bond, —O— or the like; Y 2 represents a lower alkylene group or the like; W1 to W4 independently represent a single bond, a methylene group or the like; L represents a single bond, a methylene group or the like; Z 1 and Z 2 independently represent a single bond, a C 1-4 alkylene group or the like; Ar 1 represents an aromatic carbocyclic ring or the like; and Ar 2 represents a bicyclic aromatic carbocyclic ring or the like. The compound is useful as a pharmaceutical for a central disease, a cardiovascular disease or a metabolic disease.
    本发明揭示了一种化合物,其化学式为(I):其中R1和R2分别代表氢原子、低碳烷基或类似物;X1、X2和X3分别代表亚甲基基团或氮原子;Y1和Y3分别代表单键、—O—或类似物;Y2代表低碳烷基基团或类似物;W1至W4独立地代表单键、亚甲基基团或类似物;L代表单键、亚甲基基团或类似物;Z1和Z2独立地代表单键、C1-4烷基基团或类似物;Ar1代表芳香环烷基环或类似物;Ar2代表双环芳香环烷基环或类似物。该化合物可用作治疗中枢疾病、心血管疾病或代谢性疾病的药物。
  • BICYCLIC AROMATIC SUBSTITUTED PYRIDONE DERIVATIVE
    申请人:BANYU PHARMACEUTICAL CO., LTD.
    公开号:EP1939194A1
    公开(公告)日:2008-07-02
    Disclosed is a compound represented by the formula (I): Wherein R1 and R2 independently represent a hydrogen atom, a lower alkyl group or the like; X1 , X2 and X3 independently represent a methine group or a nitrogen atom; Y1 and Y3 independently represent a single bond, -O- or the like; Y2 represents a lower alkylene group or the like; W1 to W4 independently represent a single bond, a methylene group or the like; L represents a single bond, a methylene group or the like; Z1 and Z2 independently represent a single bond, a C1-4 alkylene group or the like; Ar1 represents an aromatic carbocyclic ring or the like; and Ar2 represents a bicyclic aromatic carbocyclic ring or the like. The compound is useful as a pharmaceutical for a central disease, a cardiovascular disease or a metabolic disease.
    本发明公开了一种由式 (I) 表示的化合物: 其中 R1 和 R2 独立地代表氢原子、低级烷基或类似物;X1、X2 和 X3 独立地代表甲基或氮原子;Y1 和 Y3 独立地代表单键、-O- 或类似物;Y2 代表低级亚烷基或类似物;W1 至 W4 独立地代表单键、亚甲基或类似物;L 代表单键、亚甲基或类似物;Z1 和 Z2 独立地代表单键、C1-4 亚烷基或类似物;Ar1 代表芳香碳环或类似物;Ar2 代表双环芳香碳环或类似物。该化合物可用作治疗中枢疾病、心血管疾病或代谢疾病的药物。
  • Organic light-emitting device
    申请人:SAMSUNG DISPLAY CO., LTD.
    公开号:US10312449B2
    公开(公告)日:2019-06-04
    An organic light-emitting device including a first electrode, a second electrode, and an organic layer between the first electrode and the second electrode and including an emission layer; wherein the organic layer includes a host first compound represented by Formula 1 and a fluorescent dopant second compound represented by Formula 2: When the compound represented by Formula 1 includes a condensed cyclic substituent and the compound represented by Formula 2 includes a condensed cyclic core, the organic light-emitting device may have improved thermal stability, a lower driving voltage, and higher efficiency.
    一种有机发光器件,包括第一电极、第二电极以及位于第一电极和第二电极之间并包括发射层的有机层;其中有机层包括由式 1 表示的宿主第一化合物和由式 2 表示的荧光掺杂剂第二化合物: 当式 1 所代表的化合物包括缩合环取代基和式 2 所代表的化合物包括缩合环核心时,有机发光器件可能具有更好的热稳定性、更低的驱动电压和更高的效率。
  • ORGANIC LIGHT-EMITTING DEVICE
    申请人:Samsung Display Co., Ltd.
    公开号:US20170186975A1
    公开(公告)日:2017-06-29
    An organic light-emitting device includes: a first electrode; a second electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer, wherein the organic layer includes a first compound represented by Formula 1 and a second compound represented by Formula 2, wherein a case where the first compound is 4,4′-bis(N-carbazolyl)-1,1′-biphenyl(CBP) is excluded:
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