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methyl 2-prop-2-enyl-2H-chromene-3-carboxylate | 1010721-87-5

中文名称
——
中文别名
——
英文名称
methyl 2-prop-2-enyl-2H-chromene-3-carboxylate
英文别名
——
methyl 2-prop-2-enyl-2H-chromene-3-carboxylate化学式
CAS
1010721-87-5
化学式
C14H14O3
mdl
——
分子量
230.263
InChiKey
GQSMQLGIZAJFAB-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):
    3
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    methyl 2-[(4-methylphenyl)sulfonylamino]-2H-chromene-3-carboxylate烯丙基三甲基硅烷四氯化钛 作用下, 以 四氢呋喃甲苯 为溶剂, 反应 3.0h, 以23 mg的产率得到methyl 2-prop-2-enyl-2H-chromene-3-carboxylate
    参考文献:
    名称:
    Three-Component Coupling Reaction and Cyclization of N-Tosylimines and TMS-Substituted Propiolate Mediated by DABCO
    摘要:
    [GRAPHICS]A new three-component coupling reaction of methyl 3-trimethylsilylpropiolate, N-tosylimine, and tosylamide mediated by DABCO was developed. This reaction was based on the consecutive alpha- and beta-activation method of propiolate involving intramolecular silyl migration previously developed by our group. On the basis of these results, a new cyclization reaction was designed to find a chrome ne-formin g reaction utilizing salicyl N-tosylimine as a bifunctional substrate.
    DOI:
    10.1021/jo702649q
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文献信息

  • Three-Component Coupling Reaction and Cyclization of <i>N</i>-Tosylimines and TMS-Substituted Propiolate Mediated by DABCO
    作者:Yuji Matsuya、Kousuke Hayashi、Akiho Wada、Hideo Nemoto
    DOI:10.1021/jo702649q
    日期:2008.3.1
    [GRAPHICS]A new three-component coupling reaction of methyl 3-trimethylsilylpropiolate, N-tosylimine, and tosylamide mediated by DABCO was developed. This reaction was based on the consecutive alpha- and beta-activation method of propiolate involving intramolecular silyl migration previously developed by our group. On the basis of these results, a new cyclization reaction was designed to find a chrome ne-formin g reaction utilizing salicyl N-tosylimine as a bifunctional substrate.
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