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2-[2-(2-furyl)-2-thioxoethylidene]dihydro[1,3]dithiolo[4,6-c]furan-2,5-dione | 1025026-86-1

中文名称
——
中文别名
——
英文名称
2-[2-(2-furyl)-2-thioxoethylidene]dihydro[1,3]dithiolo[4,6-c]furan-2,5-dione
英文别名
——
2-[2-(2-furyl)-2-thioxoethylidene]dihydro[1,3]dithiolo[4,6-c]furan-2,5-dione化学式
CAS
1025026-86-1
化学式
C11H6O4S3
mdl
——
分子量
298.364
InChiKey
BFMPHFKXOJXEEI-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):
    2.14
  • 重原子数:
    18.0
  • 可旋转键数:
    2.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    56.51
  • 氢给体数:
    0.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    2-[2-(2-furyl)-2-thioxoethylidene]dihydro[1,3]dithiolo[4,6-c]furan-2,5-dione氢氧化钾 作用下, 反应 1.0h, 以71.26%的产率得到2-[2-(2-furyl)-2-thioxoethylidene]-1,3-dithiolane-4,5-dicarboxylic acid
    参考文献:
    名称:
    Thiafulvenes and Thiafulvalenes in Organic Chemistry: Synthesis and Study its Behavior towards Some Chemical Reagents
    摘要:
    Trithiafulvenes were prepared through cycloaddition of 3-thioxo-1,2-dithioles to several electrophilic alkenes and alkynes. Treatments of the product with phenylhydrazine and malononitrile afforded the hydrazone and the dinitrilene derivatives respectively. The bromination and subsequent treatment with KCN and malononitrile afforded the diene derivative. The aniline derivative was also obtained by treatment with chloroaniline.
    DOI:
    10.1080/10426500701407730
  • 作为产物:
    描述:
    3,3-dimercapto-1-(2-furyl)-2-propen-1-one 在 phosphorus pentsulfide 作用下, 以 xylene 、 为溶剂, 反应 7.0h, 生成 2-[2-(2-furyl)-2-thioxoethylidene]dihydro[1,3]dithiolo[4,6-c]furan-2,5-dione
    参考文献:
    名称:
    Thiafulvenes and Thiafulvalenes in Organic Chemistry: Synthesis and Study its Behavior towards Some Chemical Reagents
    摘要:
    Trithiafulvenes were prepared through cycloaddition of 3-thioxo-1,2-dithioles to several electrophilic alkenes and alkynes. Treatments of the product with phenylhydrazine and malononitrile afforded the hydrazone and the dinitrilene derivatives respectively. The bromination and subsequent treatment with KCN and malononitrile afforded the diene derivative. The aniline derivative was also obtained by treatment with chloroaniline.
    DOI:
    10.1080/10426500701407730
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