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5,5-dimethyl-3-(2-thiosemicarbazonopropyl)tetrahydrofuran-2-one | 303965-77-7

中文名称
——
中文别名
——
英文名称
5,5-dimethyl-3-(2-thiosemicarbazonopropyl)tetrahydrofuran-2-one
英文别名
5,5-Dimethyl-3-(2-thiosemicarbazonopropyl)-tetrahydrofuran-2-one;[1-(5,5-dimethyl-2-oxooxolan-3-yl)propan-2-ylideneamino]thiourea
5,5-dimethyl-3-(2-thiosemicarbazonopropyl)tetrahydrofuran-2-one化学式
CAS
303965-77-7
化学式
C10H17N3O2S
mdl
——
分子量
243.33
InChiKey
GVWJKWINDZCJTD-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):
    0.3
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    109
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    5,5-dimethyl-3-(2-oxopropyl)tetrahydrofuran-2-one 、 氨基硫脲硫酸 作用下, 以 乙醇 为溶剂, 反应 1.0h, 以80%的产率得到5,5-dimethyl-3-(2-thiosemicarbazonopropyl)tetrahydrofuran-2-one
    参考文献:
    名称:
    Synthesis of 5-substituted 3-(2-oxopropyl)tetrahydrofuran-2-ones and heterocyclic compounds on their base
    摘要:
    Alkylation of ethyl 2-oxotetrahydrofuran-3-carboxylates with 2,3-dichloroprop-1-ene and 3-bromoprop-1-yne gave new 3,5,5-tri- and 3,3,5,5-tetrasubstituted tetrahydrofuran-2-ones which were converted into the corresponding 3-(2-oxopropyl)tetrahydrofuran-2-ones. Reactions of the latter with semicarabazide, thiosemicarbazide, and phenylhydrazine were studied with a view to obtain new heterocyclic lactones.
    DOI:
    10.1134/s1070428008120130
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文献信息

  • Synthesis of 5-substituted 3-(2-oxopropyl)tetrahydrofuran-2-ones and heterocyclic compounds on their base
    作者:T. V. Kochikyan、E. V. Arutyunyan、V. S. Arutyunyan、A. A. Avetisyan
    DOI:10.1134/s1070428008120130
    日期:2008.12
    Alkylation of ethyl 2-oxotetrahydrofuran-3-carboxylates with 2,3-dichloroprop-1-ene and 3-bromoprop-1-yne gave new 3,5,5-tri- and 3,3,5,5-tetrasubstituted tetrahydrofuran-2-ones which were converted into the corresponding 3-(2-oxopropyl)tetrahydrofuran-2-ones. Reactions of the latter with semicarabazide, thiosemicarbazide, and phenylhydrazine were studied with a view to obtain new heterocyclic lactones.
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