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5,7-dioxo(4H,6H)-1,3-dithiolo<4,5-d>pyrimidine-2-selenone | 144339-77-5

中文名称
——
中文别名
——
英文名称
5,7-dioxo(4H,6H)-1,3-dithiolo<4,5-d>pyrimidine-2-selenone
英文别名
5,7-dioxo(4H,6H)-1,3-dithiolo<4,5-d>pyrimidineselenone-2;5,7-dioxo(4H,6H)-1,3-dithiolo<4,5-d>pyrimidine-2-selone;5,7-dioxo-(4H,6H)-1,3-dithiolo[4,5-d]pyrimidine-2-selenone;5,7-dioxo(4H,6H)-1,3-dithiolo[4,5-d]pyrimidine-2-selone;2-selanylidene-4H-[1,3]dithiolo[4,5-d]pyrimidine-5,7-dione
5,7-dioxo(4H,6H)-1,3-dithiolo<4,5-d>pyrimidine-2-selenone化学式
CAS
144339-77-5
化学式
C5H2N2O2S2Se
mdl
——
分子量
265.175
InChiKey
JCFVOYUCQBRJOW-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):
    0.04
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    109
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

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文献信息

  • Synthesis and X-ray crystal structure of a novel tetrathiafulvalene dimethyl[2,4-dioxo(1H,3H)pyrimido]tetrathiafulvalene, able to form intermolecular hydrogen bonds of nucleic acid base-pair type
    作者:Ojars Neilands、Sergey Belyakov、Vija Tilika、Alma Edžina
    DOI:10.1039/c39950000325
    日期:——
    The efficient synthesis, molecular and crystal structure, chemical, spectroscopical and electrochemical properties and charge-transfer salts of dimethyl[2,4-dioxo(1H,3H)pyrimido]tetrathiafulvalene, a novel π-electron donor able to form intermolecular hydrogen bonds of nucleic acid base-pair type, are described.
    二甲基[2,4-二氧(1 H,3 H)嘧啶基]四硫富瓦烯的合成,分子和晶体结构,化学,光谱和电化学性质以及电荷转移盐,一种能够形成分子间氢的新型π电子供体描述了核酸碱基对类型的键。
  • Synthesis of derivatives of new heterocyclic system 5,7-dioxo(4h,6h)-1,3-dithiolo[4,5-d]pyrimidine on the basis of barbituric acid
    作者:O. Ya. Neiland、V. Yu. Khodorkovskii、V. Zh. Tilika
    DOI:10.1007/bf00531299
    日期:1992.12
  • Synthesis of Novel Tetrathiafulvalene System Containing Redox-Active Ribonucleoside and Oligoribonucleotide
    作者:Ojars Neilands、Vilnis Liepinsh、Baiba Turovska
    DOI:10.1021/ol9910868
    日期:1999.12.1
    [GRAPHICS]RNA oligosynthesis block 8 was synthesized from selone 1 by successive silylation, acetylribosylation, coupling with selone 4, desacetylation, and treatment of obtained ribonucleoside 6 with monomethoxytrityl chloride, followed by o-chlorobenzoylation and phosphonylation. Solid-phase oligosynthesis is being performed, and redox-active heptaribonucleotide phosphothioate 9 is obtained which has a lower oxidation potential than ribonucleoside 6.
  • Pyrimidotetrathiafulvalenes. 2. Trimethylsilylation of 5,-dioxo(4H, 6H)-1,3-dithiolo-[4,5-d]pyrimidine-2-selone and the use of the silylated product for the synthesis of 2,4-dioxopyrimidotetrathiafulvalenes
    作者:O. Ya. Neiland、V. Zh. Tilika、A. S. Edzhinya
    DOI:10.1007/bf01171177
    日期:1994.9
  • Pyrimidotetrathiafulvalenes
    作者:O. Ya. Neiland、V. Zh. Tilika、A. S. Edzhinya
    DOI:10.1007/bf00531333
    日期:1992.8
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