摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

dibenzanthracene-9,14-dione | 3228-74-8

中文名称
——
中文别名
——
英文名称
dibenzanthracene-9,14-dione
英文别名
Dibenzoanthrachinone;dibenz(a,c)anthracene-9,14-dione;benzo[f]tetraphene-9,14-dione;benzo[b]triphenylene-9,14-dione;Benzo[b]triphenylen-9,14-dion;1.2;3.4-Dibenzo-anthrachinon;benzo[b]triphenylene-9,14-dione
dibenz<a,c>anthracene-9,14-dione化学式
CAS
3228-74-8
化学式
C22H12O2
mdl
——
分子量
308.336
InChiKey
SZMVHOFGIOFVTO-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

  • 熔点:
    179 °C
  • 沸点:
    557.5±20.0 °C(Predicted)
  • 密度:
    1.356±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    24
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:16a5449bcf7a5817e52456da7cbc80df
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Annulation selectivity in the coupling of Fischer carbene complexes with o-alkynylbiphenyl and o-alkynylstyrene derivatives
    作者:Thaddeus J Jackson、James W Herndon
    DOI:10.1016/s0040-4020(01)00227-7
    日期:2001.4
    The coupling of various Fischer carbene complexes with o-ethynylbiphenyl and an o-alkynylstyrene derivatives has been examined. In coupling reactions with methylcarbene and cyclopropylcarbene complexes, the major products are derived from C–H or C–C activation processes. In coupling reactions with phenylcarbene complexes, the major products are derived from the Dötz reaction.
    已经研究了各种费歇尔卡宾配合物与邻乙炔基联苯和邻炔基苯乙烯衍生物的偶联。与甲基卡宾和环丙基卡宾络合物的偶联反应中,主要产物来自C–H或C–C活化过程。与苯基卡宾配合物的偶联反应中,主要产物来自Dötz反应。
  • Synthesis of dibenzo[<i>a</i>,<i>d</i>]cycloheptanoids <i>via</i> aryne insertion into 2-arylidene-1,3-indandiones
    作者:Nagaraju Payili、Santhosh Reddy Rekula、Anjaiah Aitha、V. V. S. R. N. Anji Karun Mutha、Challa Gangu Naidu、Satyanarayana Yennam
    DOI:10.1039/c9ob01900f
    日期:——
    A novel and unexpected aryne insertion cascade reaction on 2-arylidene-1,3-indandiones via conjugate addition of fluoride followed by formal C-C insertion is developed to afford dibenzo[a,d]cycloheptanoid derivatives in good yields with a single isomer. This reaction represents a rare instance of cyclic enone C-C bond insertion (acyl-alkenylation) in aryne chemistry. Interestingly, 2-arylidene-1,3-indandiones
    通过共轭添加氟化物,然后通过正式的CC插入,在2-芳基-1,3-茚满二酮上进行了新颖且出乎意料的芳烃插入级联反应,从而以单一异构体的高收率得到了二苯并[a,d]环庚烷衍生物。该反应代表了在芳烃化学中罕见的环状烯酮CC键插入(酰基-烯基化)的情况。有趣的是,带有富电子官能团的2-亚芳基-1,3-茚满二酮通过[4 + 2]环加成反应然后扩环提供二苯并[a,c]蒽-9,14-二酮衍生物。
  • Electrochemical display device
    申请人:Western Electric Company, Incorporated
    公开号:EP0019919A2
    公开(公告)日:1980-12-10
    Display devices are described which include at least one positive and at least one negative electrode and an electrochemical solution containing a suitable organic solvent, an active material containing species which change color under the influence of an electrical signal, and an electrolyte, the improvement residing in the use of organic quinones or diodes as the said active material. These devices exhibit high optical contrast, pleasing and striking colors and unusually low power consumption. Particularly advantageous is the fact that these display devices may exhibit non-linear behavior (sharp thresholds) which permit multiplexing. This is highly advantageous in display device applications.
    所述显示装置包括至少一个正电极和至少一个负电极,以及含有适当有机溶剂的电化学溶液、含有在电信号影响下会变色的物质的活性材料和电解液,改进之处在于使用有机醌或二极管作为上述活性材料。这些装置具有光学对比度高、色彩悦目醒目、功耗极低的特点。特别有利的是,这些显示器件可以表现出非线性行为(尖锐的阈值),从而允许多路复用。这在显示设备应用中非常有利。
  • Dibenzoanthraquinone based chromophores
    申请人:——
    公开号:US20020096084A1
    公开(公告)日:2002-07-25
    An infrared dye, characterized in that the dye comprises a compound that comprises a molecule that can be described by claim 1.
    一种红外染料,其特征在于,该染料包含一种由权利要求 1 所述分子组成的化合物。
  • Tandem directed metalation reactions. Short syntheses of polycyclic aromatic hydrocarbons and ellipticine alkaloids
    作者:M. Watanabe、V. Snieckus
    DOI:10.1021/ja00524a059
    日期:1980.2
查看更多

同类化合物

酒色霉素 A1 萘并[1,2-b]菲-7,14-二酮 苯并蒽-7,12-二酮 腊伯罗霉素 浅内红霉素 水绫霉素 棣棠霉素 C 抑胃酶氨酰-21 富士霉素A 四角霉素 丙酸,2-甲基-,(3R,4S)-1,2,3,4,7,12-六氢-8-甲氧基-3-甲基-1,7,12-三羰基苯并[a]蒽-4-基酯 丁二酸,碘-,4-乙基1-甲基酯(9CI) N-{4-[(4-吡啶-2-基哌嗪-1-基)羰基]苯基}-7-(三氟甲基)喹啉-4-胺 8-羟基-3-甲基-3,4-二氢-1,7,12(2H)-苯并[a]蒽三酮 8-甲氧基-3-甲基-3,4-二氢-1,7,12(2H)-四苯e三酮 8,11-二[2-(2-羟基乙基氨基)乙基氨基]-6-甲氧基-1,2,3,4-四氢苯并[a]蒽-7,12-二酮 4a,8,12b-三羟基-4-甲基-1H-苯并[a]蒽-2,7,12-三酮 3-甲氧基苯并(a)蒽-7,12-二酮 1,3-二羟基-8-甲氧基-3-甲基-2,4-二氢-1H-苯并[a]蒽-7,12-二酮 (R)-8-羟基-3-甲基-1,2,3,4-四氢苯并[a]蒽-7,12-二酮 (3S)-6-羟基-8-甲氧基-3-甲基-3,4-二氢-2H-苯并[a]蒽-1,7,12-三酮 (3S)-3-甲基-8-[(2S,3R,4R,5R,6S)-3,4,5-三羟基-6-甲基四氢吡喃-2-基]氧基-3,4-二氢-2H-苯并[a]蒽-1,7,12-三酮 (3S)-11-羟基-8-甲氧基-3-甲基-3,4-二氢-2H-苯并[a]蒽-1,7,12-三酮 (3R)-9-[(2R,4R,5R,6R)-4-[(2S,5S,6S)-5-[(2S,4R,5S,6R)-4,5-二羟基-6-甲基四氢吡喃-2-基]氧基-6-甲基四氢吡喃-2-基]氧基-5-羟基-6-甲基四氢吡喃-2-基]-3,8-二羟基-3-甲基-2,4-二氢苯并[b]菲-1,7,12-三酮 (2S,4S,5S)-4-[(1E,3E,5E)-7-[(2R,6R)-6-[(2R,3S,4aR,12bS)-2,3,4A,8,12B-五羟基-3-甲基-1,7,12-三氧代-2,4-二氢苯并[h]菲-9-基]-2-甲基四氢吡喃-3-基]氧基-7-氧代庚-1,3,5-三烯基]-2,5-二甲基-1,3-二氧戊环-2-羧酸 (2R,3S,4aR,12bS)-2,3,4a,8,12b-五羟基-3-甲基-3,4,4a,12b-四氢-1,7,12(2H)-四苯e三酮 (1S,3S)-10-[[(1S,3S)-1,11-二羟基-8-甲氧基-3-甲基-7,12-二氧代-1,2,3,4-四氢苯并[h]菲-10-基]甲基]-1,11-二羟基-8-甲氧基-3-甲基-1,2,3,4-四氢苯并[B]菲-7,12-二酮 (1S,3S)-1-羟基-8-甲氧基-3-甲基-1,2,3,4-四氢苯并[a]蒽-7,12-二酮 (-)-8-O-甲基四角霉素 methyl 9-fluoro-6-hydroxy-8-methoxy-1,2,3,4-tetrahydrobenz[a]anthracene-7,12-dione-2-carboxylate urdamycinone B amycomycin B 6-hydroxy-5-hydroxymethylbenz[a]anthracene-7,12-dione 6-hydroxy-5-methylbenz[a]anthracene-7,12-dione 6-hydroxy-1,5,8-trimethoxy-3-methyltetraphene-7,12-dione 3,6-Dihydroxy-3-methyl-1,2,3,4-tetrahydrobenzanthracene-7,12-dione Moromycin B Moromycin A 1,2,3,11,12,13-Hexamethoxydibenzanthracen-7,14-chinon 4-methoxybenzanthracene-7,12-dione Fujianmycin B (3R,4aR,12bS)-4a,8,12b-trihydroxy-9-[5-(5-hydroxy-6-methyloxan-2-yl)oxy-6-methyloxan-2-yl]-3-methyl-3-[(6-methyl-5-oxo-2H-pyran-2-yl)oxy]-2,4-dihydrobenzo[a]anthracene-1,7,12-trione 4,11-dihydroxy-dibenz[a,h]anthracene-7,14-dione 5-fluoro-1,2,3,4-tetrahydrobenzanthracene-7,12-dione 10-fluoro-1,2,3,4-tetrahydrobenzanthracene-7,12-dione 3-methoxydibenzanthracene-7,14-dione 4-Hydroxy-benzanthracen-7,12-dion 8-Methoxy-1,2,3,4-tetrahydro-benzo[a]anthracene-7,12-dione 1-Hydroxybenzantracen-7,12-chinon 8-methoxy-3-methyl-7,12-dioxy-1,2,3,4-tetrahydro-benzoanthracene-2-dimethylene dithioacetal