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  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
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  • 反应信息
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  • 同类化合物
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  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.8
  • 重原子数:
    21
  • 可旋转键数:
    0
  • 环数:
    4.0
  • 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

文献信息

  • BENZANTHRACENE DERIVATIVES FOR ORGANIC ELECTROLUMINESCENT DEVICES
    申请人:Stoessel Philipp
    公开号:US20100187505A1
    公开(公告)日:2010-07-29
    The present invention relates to the compounds of the formula (1) and to organic electroluminescent devices, in particular blue-emitting devices, in which these compounds are used as host material or dopant in the emitting layer and/or as hole-transport material and/or as electron-transport material.
    本发明涉及公式(1)的化合物,以及有机电致发光器件,特别是蓝色发光器件,在这些器件中,这些化合物被用作发射层的主体材料或掺杂剂,和/或作为空穴传输材料和/或电子传输材料。
  • Durch Einwirkung von Strahlung vernetzendes Gemisch und dessen Verwendung zur Herstellung hochtemperaturbeständiger Reliefstrukturen
    申请人:BASF Lacke + Farben Aktiengesellschaft
    公开号:EP0571899A1
    公开(公告)日:1993-12-01
    Die Erfindung betrifft durch Einwirkung von Strahlung vernetzende Gemische, im wesentlichen bestehend aus (I) mindestens einer in polaren organischen Lösungsmitteln löslichen carboxylgruppenhaltigen polymeren Vorstufe hochtemperaturbeständiger heterocyclischer Polymerer, (II) einem copolymerisierbaren ethylenisch ungesättigten ternären Sulfoniumsalz, (III) einem Photoinitiator oder Photoinitiatorsystem und (IV) mindetens einem polaren aprotischen organischen Lösungsmittel. Diese Gemische eignen sich zur Herstellung hochtemperaturbeständiger Reliefstrukturen.
    本发明涉及在辐射作用下交联的混合物,主要包括 (I) 至少一种可溶于极性有机溶剂的耐高温杂环聚合物的含羧基聚合物前体、 (II) 可共聚的乙烯不饱和三元锍盐 (III) 一种光引发剂或光引发剂体系,以及 (IV) 至少一种极性烷基有机溶剂。 这些混合物适用于生产耐高温浮雕结构。
  • Developing solution and method of forming polyimide pattern by using the developing solution
    申请人:Yoshiaki Kawamonzen
    公开号:US20010006767A1
    公开(公告)日:2001-07-05
    Disclosed is a developing solution for a photosensitive polyimide, which consists of an aqueous solution of an amine compound having a base dissociation index pKb [=−log (Kb)=−log (Kw/Ka)=14−pKa, where Kb is a base dissociation constant, Ka is acid dissociation constant of a proton complex, pKa is an acid dissociation index of a proton complex=−log (Ka), and Kw is an ion product of water=1×10 −14 ] of 5 to 8 within an aqueous solution of 25° C.
    本发明公开了一种用于感光聚酰亚胺的显影液,它由一种胺化合物的水溶液组成,该胺化合物的碱解离指数为 pKb [=-log (Kb)=-log (Kw/Ka)=14-pKa,其中 Kb 是碱解离常数,Ka 是质子络合物的酸解离常数,pKa 是质子络合物的酸解离指数=-log (Ka),Kw 是水的离子积=1×10 -14 ]在 25° C 的水溶液中为 5 至 8。
  • Resin-encapsulated semiconductor apparatus and process for its fabrication
    申请人:Hitachi, Ltd.
    公开号:US20020027268A1
    公开(公告)日:2002-03-07
    The present invention provides a resin-encapsulated semiconductor apparatus comprising a semiconductor device having a ferroelectric film and a surface-protective film, and an encapsulant member comprising a resin; the surface-protective film being formed of a polyimide. The present invention also provides a process for fabricating a resin-encapsulated semiconductor apparatus, comprising the steps of forming a film of a polyimide precursor composition on the surface of a semiconductor device having a ferroelectric film; heat-curing the polyimide precursor composition film to form a surface-protective film formed of a polyimide; and encapsulating, with an encapsulant resin, the semiconductor device on which the surface-protective film has been formed. The polyimide may preferably have a glass transition temperature of from 240° C. to 400° C. and a Young's modulus of from 2,600 MPa to 6 GPa. The curing may preferably be carried out at a temperature of from 230° C. to 300° C.
    本发明提供了一种树脂封装半导体装置,该装置包括具有铁电薄膜和表面保护膜的半导体器件,以及由树脂组成的封装件;表面保护膜由聚酰亚胺形成。本发明还提供了一种制造树脂封装半导体设备的工艺,包括以下步骤:在具有铁电薄膜的半导体设备表面形成聚酰亚胺前体组合物薄膜;热固化聚酰亚胺前体组合物薄膜,形成由聚酰亚胺构成的表面保护膜;以及用封装树脂封装已形成表面保护膜的半导体设备。聚酰亚胺最好具有 240°C 至 400°C 的玻璃转化温度和 2,600 MPa 至 6 GPa 的杨氏模量。固化最好在 230 摄氏度至 300 摄氏度的温度下进行。
  • NEWMAN, M. S.;PRABHU, V. S.;VEERARAGHAVAN, S., J. ORG. CHEM., 1983, 48, N 17, 2926-2928
    作者:NEWMAN, M. S.、PRABHU, V. S.、VEERARAGHAVAN, S.
    DOI:——
    日期:——
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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