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8-benzyloxy-1,2-di(hexyloxy)-5-methyldibenzo[cd,f]indol-4(5H)-one | 1144527-23-0

中文名称
——
中文别名
——
英文名称
8-benzyloxy-1,2-di(hexyloxy)-5-methyldibenzo[cd,f]indol-4(5H)-one
英文别名
14,15-Dihexoxy-10-methyl-5-phenylmethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one
8-benzyloxy-1,2-di(hexyloxy)-5-methyldibenzo[cd,f]indol-4(5H)-one化学式
CAS
1144527-23-0
化学式
C35H41NO4
mdl
——
分子量
539.715
InChiKey
AVUDYZKQJAIQHO-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):
    9.6
  • 重原子数:
    40
  • 可旋转键数:
    15
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    48
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 下游产品
    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:
    8-benzyloxy-1,2-di(hexyloxy)-5-methyldibenzo[cd,f]indol-4(5H)-one 在 palladium 10% on activated carbon 氢气 作用下, 以 甲醇 为溶剂, 反应 3.0h, 以97%的产率得到8-hydroxy-1,2-di(hexyloxy)-5-methyldibenzo[cd,f]indol-4(5H)-one
    参考文献:
    名称:
    [EN] PHENANTHRENE LACTAM DERIVATIVES HAVING ANTICANCER ACTIVITY AND METHOD FOR THE PREPARATION THEREOF
    [FR] DÉRIVÉS DE LACTAME PHÉNANTHRÈNE PRÉSENTANT UNE ACTIVITÉ ANTICANCÉREUSE ET PROCÉDÉ DE PRÉPARATION DE CEUX-CI
    摘要:
    公开号:
    WO2009051417A3
  • 作为产物:
    描述:
    4-bromo-5,6-bis(hexyloxy)-2-methylisoindolin-1-one 、 4-苄氧基-2-醛基苯硼酸四(三苯基膦)钯caesium carbonate 作用下, 以 乙醇甲苯 为溶剂, 反应 0.25h, 以86%的产率得到8-benzyloxy-1,2-di(hexyloxy)-5-methyldibenzo[cd,f]indol-4(5H)-one
    参考文献:
    名称:
    Identification of Vimentin Binding to the Derivative of Saurolactam with Antiresorptive Activity by Using Its Chemical Affinity Probe
    摘要:
    DOI:
    10.5012/bkcs.2010.31.7.2047
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文献信息

  • [EN] PHENANTHRENE LACTAM DERIVATIVES HAVING ANTICANCER ACTIVITY AND METHOD FOR THE PREPARATION THEREOF<br/>[FR] DÉRIVÉS DE LACTAME PHÉNANTHRÈNE PRÉSENTANT UNE ACTIVITÉ ANTICANCÉREUSE ET PROCÉDÉ DE PRÉPARATION DE CEUX-CI
    申请人:KOREA RES INST CHEM TECH
    公开号:WO2009051417A3
    公开(公告)日:2009-06-04
  • Identification of Vimentin Binding to the Derivative of Saurolactam with Antiresorptive Activity by Using Its Chemical Affinity Probe
    作者:Myung-Hee Kim、Young-Lok Choi、Jung-Nyoung Heo、Yong-Ki Min、Seong-Hwan Kim
    DOI:10.5012/bkcs.2010.31.7.2047
    日期:2010.7.20
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同类化合物

马兜铃内酰胺FI 马兜铃内酰胺BIII 马兜铃内酰胺AII 马兜铃内酰胺-葡糖苷 马兜铃内酰胺-II 马兜铃内酰胺 BII 马兜铃内酰胺 胡椒内酰胺 C; 2-O-甲基马兜铃 乙氧基马兜铃内酰胺 8-氯-1,2-二甲氧基-5-甲基二苯并[cd,f]吲哚-4-(5H)-酮 2-羟基-1-甲氧基-5-甲基二苯并(cd,f)吲哚-4(5H)-酮 1-羟基-2,7-二甲氧基二苯并[CD,F]吲哚-4(5H)-酮 1,2,8-三甲氧基-5-甲基二苯并[cd,f]吲哚-4-(5H)-酮 (E)-6-(6-O-(3-(4-羟基苯基)-1-氧代-2-丙烯基)-beta-D-吡喃葡萄糖基)-8-甲氧基-苯并(f)-1,3-苯并二氧戊环并(6,5,4-cd)吲哚-5(6H)-酮 8-benzyloxy-1,2-di(hexyloxy)-5-methyldibenzo[cd,f]indol-4(5H)-one 5-benzyl-1,2-dimethoxydibenzo[cd,f]indol-4(5H)-one aristololactam GZ1 1,2-dimethoxy-5-(2-morpholinoethyl)dibenzo[cd,f]indol-4(5H)-one 1,2-dimethoxy-5-propargyldibenzo[cd,f]indol-4(5H)-one 5-(cyclopropylmethyl)-1,2-dimethoxydibenzo[cd,f]indol-4(5H)-one 8-chloro-1,2-dimethoxy-5-(2-piperidin-1-yl)ethyldibenzo-[cd,f]indole-4(5H)-one 1,2,9-trimethoxy-5-(2-(piperidin-1-yl)ethyl)dibenzo[cd,f]indole-4(5H)-one 1,2,8,9-tetramethoxy-5-(2-(piperidin-1-yl)ethyl)dibenzo[cd,f]indole-4(5H)-one 1,2-dimethoxy-6-methyl-5-(2-(piperidin-1-yl)ethyl)dibenzo[cd,f]indol-4(5H)-one 1,2-dimethoxy-8-hydroxy-5-methyldibenzo[cd,f]indol-4(5H)-one 8-hydroxy-1,2-di(hexyloxy)-5-methyldibenzo[cd,f]indol-4(5H)-one aristolactam-N-β-D-glucoside 1,2-dihydroxy-7-methoxydibenzo[cd,f]indol-4(5H)-one 6-chloro-1,2-dihydroxy-7-methoxydibenzo[cd,f]indol-4(5H)-one 1,2-dimethoxy-5,6-dimethyldibenzo[cd,f]indol-4(5H)-one 8-benzyloxy-1,2-dimethoxy-5-methyldibenzo[cd,f]indol-4(5H)-one 13-[2-(Dimethylamino)ethyl]-17,18-dimethoxy-6,8-dioxa-13-azapentacyclo[10.6.1.02,10.05,9.015,19]nonadeca-1,3,5(9),10,12(19),15,17-heptaen-14-one 17,18-Dimethoxy-13-(2-piperidin-1-ylethyl)-6,8-dioxa-13-azapentacyclo[10.6.1.02,10.05,9.015,19]nonadeca-1,3,5(9),10,12(19),15,17-heptaen-14-one 14,16-Dihydroxy-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 1,2-Dihydroxy-5H-dibenzo[cd,f]indol-4-one 6-Chloro-1,2-dihydroxy-5H-dibenzo[cd,f]indol-4-one 7-(benzyloxy)-1,2-dimethoxy-5-[(4-methoxyphenyl)methyl]-dibenz[cd,f]indol-4(5H)-one 1,2-dimethoxy-5,9-dimethyldibenzo[cd,f]indol-4-(5H)-one 1,2,7-trihydroxydibenzo[cd,f]indol-4(5H)-one aristolactam C N-β-D-glucoside 1,2-dimethoxy-5-(pyridin-4-ylmethyl)dibenzo[cd,f]indol-4(5H)-one 5-(4-t-butylphenyl)-1,2-dimethoxydibenzo[cd,f]indol-4(5H)-one 1,2-dimethoxy-5-(2-methoxy)ethyldibenzo[cd,f]indol-4(5H)-one 1,2-dimethoxy-5-ethyldibenzo[cd,f]indol-4(5H)-one 1,2-dimethoxy-5-phenethyldibenzo[cd,f]indol-4(5H)-one 1,2-dimethoxy-5-isopropyldibenzo[cd,f]indol-4(5H)-one 1,2-dimethoxy-5-(2-piperidin-1-yl)ethyldibenzo[cd,f]indole-4(5H)-one 1,2-dimethoxy-5-(4-methoxyphenyl)dibenzo[cd,f]indol-4(5H)-one enterocarpam I 16-Hydroxy-14-methoxy-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one