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2,5-dicyano-3,4-dihydroxyselenophene | 610307-67-0

中文名称
——
中文别名
——
英文名称
2,5-dicyano-3,4-dihydroxyselenophene
英文别名
3,4-Dihydroxyselenophene-2,5-dicarbonitrile
2,5-dicyano-3,4-dihydroxyselenophene化学式
CAS
610307-67-0
化学式
C6H2N2O2Se
mdl
——
分子量
213.054
InChiKey
KVANLZQJJPOTSZ-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):
    -0.1
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    88
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    2,5-dicyano-3,4-dihydroxyselenophene碘苯二乙酸溶剂黄146 作用下, 以 二氯甲烷 为溶剂, 反应 4.5h, 生成 Selenolo[3,4-b]quinoxaline-1,3-dicarbonitrile
    参考文献:
    名称:
    Synthesis of Stable Seleno[3,4-b]quinoxaline Derivatives
    摘要:
    [GRAPHIC]The unstable seleno[2,3-b]quinoxoline was generated and functionalized in situ to give the stable dialdehyde and diester derivatives. The dicyano compound was made in several steps from biscyanomethyl selenide and was found to be very stable.
    DOI:
    10.1021/ol035488y
  • 作为产物:
    描述:
    草酸二乙酯 、 bis(cyanomethyl)selenide 在 sodium硫酸 作用下, 以 乙醇 为溶剂, 反应 15.0h, 以39%的产率得到2,5-dicyano-3,4-dihydroxyselenophene
    参考文献:
    名称:
    Synthesis of Stable Seleno[3,4-b]quinoxaline Derivatives
    摘要:
    [GRAPHIC]The unstable seleno[2,3-b]quinoxoline was generated and functionalized in situ to give the stable dialdehyde and diester derivatives. The dicyano compound was made in several steps from biscyanomethyl selenide and was found to be very stable.
    DOI:
    10.1021/ol035488y
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文献信息

  • Synthesis of Stable Seleno[3,4-<i>b</i>]quinoxaline Derivatives
    作者:Emad Aqad、M. V. Lakshmikantham、Michael P. Cava
    DOI:10.1021/ol035488y
    日期:2003.10.1
    [GRAPHIC]The unstable seleno[2,3-b]quinoxoline was generated and functionalized in situ to give the stable dialdehyde and diester derivatives. The dicyano compound was made in several steps from biscyanomethyl selenide and was found to be very stable.
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同类化合物

硒酚 硒吩并[3,2-B]噻吩 硒吩-3-羧酸 硒吩-2-羧酸 硒吩-2-硼酸 5-甲基-2-硒吩羰基氯化物 5-甲基-2-硒吩亚磺酸 3-硒吩羰基氯化物 3-甲基硒吩 3,4-双(氯甲基)-2,5-二甲基硒吩 2-甲基-硒吩 2-乙烯基硒吩 2,5-二-(2'-噻吩基)硒吩 2,2'-双硒 2,6-di(selenophen-2-yl)tetrahydro-4H-selenopyran-4-one 2-(2-(selenophen-2-yl)ethynyl)selenophene (2-selenophene-2-yl)lithium 2-(dec-1-ynyl)selenophene (3-selenienyl)di(1-adamantyl)methanol 5-Methyl-2-mercapto-selenophen seleno[3,4-b]thiophene 3-Selenophenethiol, 2,5-dimethyl- 2-dicyanomethylselenophene bis(3-selenienyl)methanol 2-Propyl-selenophen 2-(5'-hydroxymethyl-2'-selenyl)-thiophene 4,4,6,6-tetramethyl-2-{[(methylsulfonyl)thio]methyl}-4,6-dihydro-5H-selenolo[2,3-c]pyrrol-5-yloxyl radical selenosulflower 5-Carboxyseleno<2,3-b>thiophen methyl 4-[(dimethylamino)diazenyl]-5-methylselenophene-2-carboxylate ethyl selenopheno[3,2-b]thiophene-5-carboxylate 3-Cyanoselenophen 2,4-Ditert-butylselenophene 5-Hydroxymethyl-selenophen-2-carbonsaeure 1,3-Dithiolo<4,5-c>selenophene-2-thione methyl 3-amino-5-(methoxycarbonyl)selenophene-2-carboxylate tetramethyl 2,3,4,5-selenophenetetracarboxylate 2,2'-{5,5'-[5,5'-(selenophene-2,5-diyl)bis(3,4-dibutylthien-5,2-diyl)]bis-(selenophene-5,2-diyl)}bis(methan-1-yl-1-ylidene)dimalononitrile 2-(2-bromoethylsulfonyl)selenophene 2-(4,4-bis(methoxymethyl)-7-(selenophen-2-yl)hepta-1,6-diynyl)selenophene cyclopenta[c]selenophene-(CH2OMe)2 2-[5,5-Bis(methoxymethyl)-3-thiophen-2-yl-4,6-dihydrocyclopenta[c]selenophen-1-yl]thiophene 3,6-dimethylselenolo<3,2-b>selenophene 2,5-Bis(2-selenienyl)furan tetramethyl-selenophene 2,3,4-trimethyl-selenophene 2,3,5-trimethyl-selenophene selenophen-2-yl-methanol 1-selenophen-2-yl-ethanol 2-carbomethoxyselenophene