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1,2-bis(2-ethoxy-5-phenyl-3-thienyl)perfluorocyclopentene | 443890-91-3

中文名称
——
中文别名
——
英文名称
1,2-bis(2-ethoxy-5-phenyl-3-thienyl)perfluorocyclopentene
英文别名
1,2-bis[2-ethoxy-5-phenyl-3-thienyl]perfluorocyclopentene;1,2-Bis(2-ethoxy-5-phenyl-3-thienyl)-3,3,4,4,5,5-hexafluoro-1-cyclopentene;2-ethoxy-3-[2-(2-ethoxy-5-phenylthiophen-3-yl)-3,3,4,4,5,5-hexafluorocyclopenten-1-yl]-5-phenylthiophene
1,2-bis(2-ethoxy-5-phenyl-3-thienyl)perfluorocyclopentene化学式
CAS
443890-91-3
化学式
C29H22F6O2S2
mdl
——
分子量
580.615
InChiKey
POKZSGZUQYDRFN-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):
    8.8
  • 重原子数:
    39
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    74.9
  • 氢给体数:
    0
  • 氢受体数:
    10

反应信息

  • 作为反应物:
    描述:
    1,2-bis(2-ethoxy-5-phenyl-3-thienyl)perfluorocyclopentene正己烷 为溶剂, 生成 9a,9b-Diethoxy-4,4,5,5,6,6-hexafluoro-2,8-diphenyl-5,6,9a,9b-tetrahydro-4H-1,9-dithia-trindene
    参考文献:
    名称:
    Dithienylethenes with a Novel Photochromic Performance
    摘要:
    Dithienylethenes with low decoloration quantum yields and thermal reversibility at high temperature above 100degreesC were prepared. Introduction of bulky alkoxy substituents at 2- and 2'-positions of the thiophene rings strongly suppressed the cycloreversion quantum yields. The quantum yields were lower than 10(-3), and the photogenerated color remained stable enough under room light. On the other hand, the bulky alkoxy substituent decreased the thermal stability of the colored closed-ring isomers at high temperature. The color of the dithienylethene with cyclohexyloxy substituents faded out in less than 1 min at 160degreesC.
    DOI:
    10.1021/jo020114o
  • 作为产物:
    参考文献:
    名称:
    Dithienylethenes with a Novel Photochromic Performance
    摘要:
    Dithienylethenes with low decoloration quantum yields and thermal reversibility at high temperature above 100degreesC were prepared. Introduction of bulky alkoxy substituents at 2- and 2'-positions of the thiophene rings strongly suppressed the cycloreversion quantum yields. The quantum yields were lower than 10(-3), and the photogenerated color remained stable enough under room light. On the other hand, the bulky alkoxy substituent decreased the thermal stability of the colored closed-ring isomers at high temperature. The color of the dithienylethene with cyclohexyloxy substituents faded out in less than 1 min at 160degreesC.
    DOI:
    10.1021/jo020114o
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文献信息

  • Pohtochromic material
    申请人:JAPAN SCIENCE AND TECHNOLOGY CORPORATION
    公开号:US20040049040A1
    公开(公告)日:2004-03-11
    A photochromic material having a ring opening quantum yield of 10 −3 or lower which does not fade under ambient light is provided. The material comprises a compound belonging to the diheteroarylethene class. The compound has alkoxy group and aryl group on the heteroaryl group.
    提供一种具有环开放量子产率为10^-3或更低且不会在常温光线下褪色的光致变色材料。该材料包括属于二杂环乙烯类的化合物。该化合物在杂环基上具有烷氧基和芳基。
  • PHOTOCHROMIC MATERIAL
    申请人:Japan Science and Technology Agency
    公开号:EP1367111B1
    公开(公告)日:2009-07-22
  • DEVELOPERS AND METHOD OF COLORING LITHOGRAPHIC PRINTING MEMBERS
    申请人:Figov Murray
    公开号:US20120045720A1
    公开(公告)日:2012-02-23
    A color contrast image in imaged lithographic printing precursors can be obtained by contacting the imaged precursor with a coloration solution containing a colorless form of a photochromic compound. Residual amounts of this compound attached to the oleophilic surface of the imaged precursor can be changed to its colored form when exposed to UV light. The coloration solution can be an alkaline or acidic developer or an alkaline or acidic solution used separately after development. The coloration solution can also be a gum solution.
  • US7057054B2
    申请人:——
    公开号:US7057054B2
    公开(公告)日:2006-06-06
  • US8420297B2
    申请人:——
    公开号:US8420297B2
    公开(公告)日:2013-04-16
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同类化合物

阿罗洛尔 阿替卡因 阿克兰酯 锡烷,(5-己基-2-噻吩基)三甲基- 邻氨基噻吩(2盐酸) 辛基5-(1,3-二氧戊环-2-基)-2-噻吩羧酸酯 辛基4,6-二溴噻吩并[3,4-b]噻吩-2-羧酸酯 辛基2-甲基异巴豆酸酯 血管紧张素IIAT2受体激动剂 葡聚糖凝胶LH-20 苯螨噻 苯并[c]噻吩-1-羧酸,5-溴-4,5,6,7-四氢-3-(甲硫基)-4-羰基-,乙基酯 苯并[b]噻吩-2-胺 苯并[b]噻吩-2-胺 苯基-[5-(4,4,5,5-四甲基-[1,3,2]二氧杂硼烷-2-基)-噻吩-2-基亚甲基]-胺 苯基-(5-氯噻吩-2-基)甲醇 苯乙酸,-α--[(1-羰基-2-丙烯-1-基)氨基]- 苯乙酰胺,3,5-二氨基-a-羟基-2,4,6-三碘- 苯乙脒,2,6-二氯-a-羟基- 腈氨噻唑 聚(3-丁基噻吩-2,5-二基),REGIOREGULAR 硝呋肼 硅烷,(3-己基-2,5-噻吩二基)二[三甲基- 硅噻菌胺 盐酸阿罗洛尔 盐酸阿罗洛尔 盐酸多佐胺 甲酮,[5-(1-环己烯-1-基)-4-(2-噻嗯基)-1H-吡咯-3-基]-2-噻嗯基- 甲基5-甲酰基-4-甲基-2-噻吩羧酸酯 甲基5-乙氧基-3-羟基-2-噻吩羧酸酯 甲基5-乙基-3-肼基-2-噻吩羧酸酯 甲基5-(氯甲酰基)-2-噻吩羧酸酯 甲基5-(氯乙酰基)-2-噻吩羧酸酯 甲基5-(氨基甲基)噻吩-2-羧酸酯 甲基5-(4-甲氧基苯基)-2-噻吩羧酸酯 甲基5-(4-甲基苯基)-2-噻吩羧酸酯 甲基5-(1,3-二氧戊环-2-基)-2-噻吩羧酸酯 甲基4-硝基-2-噻吩羧酸酯 甲基4-氰基-5-(4,6-二氨基吡啶-2-基)偶氮-3-甲基噻吩-2-羧酸酯 甲基4-氨基-5-(甲硫基)-2-噻吩羧酸酯 甲基4-{[(2E)-2-(4-氰基苯亚甲基)肼基]磺酰}噻吩-3-羧酸酯 甲基4-(氯甲酰基)-3-噻吩羧酸酯 甲基4-(氨基磺酰基氨基)-3-噻吩羧酸酯 甲基3-甲酰氨基-4-甲基-2-噻吩羧酸酯 甲基3-氨基-5-异丙基-2-噻吩羧酸酯 甲基3-氨基-5-(4-溴苯基)-2-噻吩羧酸酯 甲基3-氨基-4-苯基-5-(三氟甲基)-2-噻吩羧酸酯 甲基3-氨基-4-氰基-5-甲基-2-噻吩羧酸酯 甲基3-氨基-4-丙基-2-噻吩羧酸酯 甲基3-[[(4-甲氧基苯基)亚甲基氨基]氨基磺酰基]噻吩-2-羧酸酯