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3,4,6,7-tetrahydro-9-(1,2-dihydro-6-methoxy-2-oxoquinolin-3-yl)-3,3,6,6-tetramethyl-2H-xanthene-1,8(5H,9H)-dione | 1616269-81-8

中文名称
——
中文别名
——
英文名称
3,4,6,7-tetrahydro-9-(1,2-dihydro-6-methoxy-2-oxoquinolin-3-yl)-3,3,6,6-tetramethyl-2H-xanthene-1,8(5H,9H)-dione
英文别名
9-(6-methoxy-2-oxo-1,2-dihydroquinolin-3-yl)-3,3,6,6-tetramethyl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione;9-(6-methoxy-2-oxo-1H-quinolin-3-yl)-3,3,6,6-tetramethyl-4,5,7,9-tetrahydro-2H-xanthene-1,8-dione
3,4,6,7-tetrahydro-9-(1,2-dihydro-6-methoxy-2-oxoquinolin-3-yl)-3,3,6,6-tetramethyl-2H-xanthene-1,8(5H,9H)-dione化学式
CAS
1616269-81-8
化学式
C27H29NO5
mdl
——
分子量
447.531
InChiKey
LCKXIDSEQMLVDD-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):
    3.4
  • 重原子数:
    33
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    81.7
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-氯-6-甲氧基喹啉-3-甲醛5,5-二甲基-1,3-环己二酮 作用下, 反应 1.5h, 以84%的产率得到3,4,6,7-tetrahydro-9-(1,2-dihydro-6-methoxy-2-oxoquinolin-3-yl)-3,3,6,6-tetramethyl-2H-xanthene-1,8(5H,9H)-dione
    参考文献:
    名称:
    Water mediated catalyst-free efficient domino synthesis of 9-(quinolin-2(1H)-one)-xanthene-1,8(5H,9H)-diones using parallel synthesizer
    摘要:
    DOI:
    10.1016/j.tetlet.2014.05.015
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文献信息

  • Water mediated catalyst-free efficient domino synthesis of 9-(quinolin-2(1H)-one)-xanthene-1,8(5H,9H)-diones using parallel synthesizer
    作者:Varadhan Krishnakumar、Badal Kumar Mandal、Fazlur-Rahman Nawaz Khan、Euh Duck Jeong
    DOI:10.1016/j.tetlet.2014.05.015
    日期:2014.7
  • Efficient Synthesis and Evaluation of Antitumor Activities of Novel Functionalized 1,8-Naphthyridine Derivatives
    作者:Lei Fu、Xian Feng、Jian-Jun Wang、Zhan Xun、Jun-Die Hu、Juan-Juan Zhang、Yan-Wei Zhao、Zhi-Bin Huang、Da-Qing Shi
    DOI:10.1021/co500120b
    日期:2015.1.12
    An efficient synthesis of novel functionalized 1,8-naphthyridine and chromeno[2,3-b]quinoline derivatives via cascade reaction of 2-chloroquinoline-3-carbaldehyde and enaminones or cyclic 1,3-dicarbonyl compounds was developed. All of the 1,8-naphthyridine derivatives synthesized were evaluated for their antiproliferative properties in vitro against cancer cells and several compounds were found to have high activities.
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