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2-(2'-hydroxy[1,1';3',1'']terphenyl-5'-ylmethylidene)indan-1,3-dione

中文名称
——
中文别名
——
英文名称
2-(2'-hydroxy[1,1';3',1'']terphenyl-5'-ylmethylidene)indan-1,3-dione
英文别名
2-({6-Hydroxy-5-phenyl-[1,1'-biphenyl]-3-YL}methylidene)-2,3-dihydro-1H-indene-1,3-dione;2-[(4-hydroxy-3,5-diphenylphenyl)methylidene]indene-1,3-dione
2-(2'-hydroxy[1,1';3',1'']terphenyl-5'-ylmethylidene)indan-1,3-dione化学式
CAS
——
化学式
C28H18O3
mdl
MFCD14711155
分子量
402.449
InChiKey
PSRMTVORJHBXBA-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):
    6.4
  • 重原子数:
    31
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    1,3-茚满二酮2'-羟基-1,1':3',1''-三联苯-5'-甲醛正丁醇 为溶剂, 反应 0.5h, 以70%的产率得到2-(2'-hydroxy[1,1';3',1'']terphenyl-5'-ylmethylidene)indan-1,3-dione
    参考文献:
    名称:
    Reaction of 2′-hydroxy[1,1′;3′,1″]terphenyl-5′-carbaldehyde with 2-naphthylamine and 1,3-diketones
    摘要:
    The condensation of 2'-hydroxy[ 1.1';3', 1"]terphenyl-5'-carbaldehyde with 2-naphthylamine and 1.3-cyclohexanedione or dimedone gave 7,8,9,10,11,12-hexahydrobenzo[a]acridin-11-ones, while analogous three-component condensation with 1,3-indandione afforded azaindeno[1,2-b]phenanthren-12-one. In addition, hexahydro-2H-xanthene-1,8-diones and arylmethylenebisdiketones were isolated as by-products.
    DOI:
    10.1134/s1070428006010167
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文献信息

  • Reaction of 2′-hydroxy-1,1′: 3′,1″-terphenyl-5′-carbaldehyde with naphthalen-1-amine, quinolin-8-amine, and 1,3-diketones
    作者:A. L. Kurlovich、V. A. Tarasevich、N. G. Kozlov
    DOI:10.1134/s1070428009100133
    日期:2009.10
    Condensation of 2'-hydroxy-1,1': 3',1aEuro(3)-terphenyl-5'-carbaldehyde with naphthalen-1-amine and cyclohexane-1,3-dione, methyl 2,2-dimethyl-4,6-dioxocyclohexane-1-carboxylate, or dimedone gave the corresponding 7-(2'-hydroxy-1,1': 3',1aEuro(3)-terphenyl-5'-yl)-7,8,9,10,11,12-hexahydro-12H-benzo[c]acridin-8-ones. The reaction of 2'-hydroxy-1,1': 3',1aEuro(3)-terphenyl-5'-carbaldehyde with naphthalen-1-amine and indan-1,3-dione produced 7-(2'-hydroxy-1,1': 3',1aEuro(3)-terphenyl-5'-yl)-8H-benzo[h]indeno[1,2-b]quinolin-8-one. 7-(2'-Hydroxy-1,1': 3',1aEuro(3)-terphenyl-5'-yl)-7,8,9,10,11,12-hexahydrobenzo[b][1,10]phenanthrolin-8-ones were obtained by three-component condensation of 2'-hydroxy-1,1': 3',1aEuro(3)-terphenyl-5'-carbaldehyde with quinolin-8-amine and cyclohexane-1,3-dione, methyl 2,2-dimethyl-4,6-dioxocyclohexane-1-carboxylate, or dimedone.
  • Reaction of 2′-hydroxy[1,1′;3′,1″]terphenyl-5′-carbaldehyde with 2-naphthylamine and 1,3-diketones
    作者:N. G. Kozlov、V. A. Tarasevich、D. A. Vasilevskii、L. I. Basalaeva
    DOI:10.1134/s1070428006010167
    日期:2006.1
    The condensation of 2'-hydroxy[ 1.1';3', 1"]terphenyl-5'-carbaldehyde with 2-naphthylamine and 1.3-cyclohexanedione or dimedone gave 7,8,9,10,11,12-hexahydrobenzo[a]acridin-11-ones, while analogous three-component condensation with 1,3-indandione afforded azaindeno[1,2-b]phenanthren-12-one. In addition, hexahydro-2H-xanthene-1,8-diones and arylmethylenebisdiketones were isolated as by-products.
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同类化合物

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