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benzoylacetone mono-{2-hydroxy-ethylimine} | 7223-53-2

中文名称
——
中文别名
——
英文名称
benzoylacetone mono-{2-hydroxy-ethylimine}
英文别名
benzoylacetoneethanolimine;3-(2-Hydroxyethylimino)-1-phenylbutan-1-one
benzoylacetone mono-{2-hydroxy-ethylimine}化学式
CAS
7223-53-2
化学式
C12H15NO2
mdl
——
分子量
205.257
InChiKey
UELZWCJSSAKIIU-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

物化性质

  • 熔点:
    91.2 °C(Solv: methanol (67-56-1); water (7732-18-5)(1:1))
  • 沸点:
    359.2±27.0 °C(Predicted)
  • 密度:
    1.04±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    49.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Spectral and thermal studies of some chromium and molybdenum complexes with ONO donor Schiff bases
    摘要:
    Reactions of M(CO)(6), where M = Cr and Mo with Schiff bases prepared by the condensation of ethanolamine with either acetylacetone or benzoylacetone were investigated. The reactions of Cr(CO)(6) in benzene resulted in the formation of the tricarbonyl drivatives [Cr(CO)(3)(HL)], HL = acaceaH or baceaH. The HL proved to act as a tridentate ligand. The corresponding reactions with MO(CO)(6) in dioxane gave the oxo complexes [Mo2O6(HL)(2)] with HL was a bidentate. All prepared complexes were investigated using elemental analysis, IR, mass spectrometry, UV-vis absorption spectra and magnetic measurement. Thermal behaviors of the complexes were studied using by thermogravimetry (TG). Schemes for the thermal decomposition were proposed along with their mass fragmentation patterns. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.saa.2006.01.016
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文献信息

  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Ni: MVol.C2, 7.9, page 711 - 715
    作者:
    DOI:——
    日期:——
  • Jaeger, E. G., Zeitschrift fur Chemie, 1966, vol. 6, p. 111
    作者:Jaeger, E. G.
    DOI:——
    日期:——
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