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2-tripropylstannylmaleate | 98493-63-1

中文名称
——
中文别名
——
英文名称
2-tripropylstannylmaleate
英文别名
Tripropyl-<1.2-bis-ethoxycarbonyl-vinyl>-zinn
2-tripropylstannylmaleate化学式
CAS
98493-63-1
化学式
C17H32O4Sn
mdl
——
分子量
419.149
InChiKey
KRVPRPMOXSZMMP-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):
    4.26
  • 重原子数:
    22.0
  • 可旋转键数:
    11.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.76
  • 拓扑面积:
    52.6
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    三丙基锡丁炔二酸二乙酯 以66%的产率得到2-tripropylstannylmaleate
    参考文献:
    名称:
    Lutsenko, I. F.; Ponomarev, S. V.; Petru, O. P., Zhurnal Obshchei Khimii, 1962, vol. 32, p. 886 - 889
    摘要:
    DOI:
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文献信息

  • Kinetics of the Uncatalyzed Hydrostannation of Diethyl Acetylenedicarboxylate
    作者:John C. Cochran、Kevin L. Caran、Elizabeth A. Pierz、David M. Miller
    DOI:10.1081/sim-120021643
    日期:2003.1.6
    Hydrostannation of carbon-carbon triple bonds is usually catalyzed by a free radical initiator or by metal complexes of palladium, molybdenum or rhodium. However, when the triple bond is substituted with an effective electron-withdrawing group, the addition reaction will proceed in the absence of a catalyst. In this paper we report the kinetics of hydrostannation of diethyl acetylenedicarboxylate, (1), with trimethylstannane (2a), tri-n-propylstannane (2b), tri-n-butylstannane (2c), and triphenylstannane, (2d). Rate constants for these reactants were determined in acetonitrile at 25, 35, and 45 degreesC. Also, rate constants for trimethylstannane and tripropylstannane were determined in cyclohexane and trimethylstannane-d(1) (2e), in acetonitrile. Finally, the hydrostannation with tributylstannane was run at 25, 35, and 45 degreesC in 95% ethanol. Where appropriate, enthalpies and entropies of activation were determined.
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Sn: Org.Verb.2, 1.1.2.3.2, page 259 - 263
    作者:
    DOI:——
    日期:——
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