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ethyl-malonic acid dihydrazide | 25457-53-8

中文名称
——
中文别名
——
英文名称
ethyl-malonic acid dihydrazide
英文别名
Aethyl-malonsaeure-dihydrazid;Monoethyl-malonsaeuredihydrazid;Monoethylmalonsaeure-dihydrazid;Ethyl-malonsaeurebishydrazid;Ethylmaloylhydrazid;Propanedioic acid, ethyl-, dihydrazide;2-ethylpropanedihydrazide
ethyl-malonic acid dihydrazide化学式
CAS
25457-53-8
化学式
C5H12N4O2
mdl
MFCD00093418
分子量
160.176
InChiKey
HNSKYWPKSJEQTA-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:
    166 °C(Solv: ethanol (64-17-5))
  • 沸点:
    488.9±28.0 °C(Predicted)
  • 密度:
    1.225±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.6
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    110
  • 氢给体数:
    4
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2928000090

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    ethyl-malonic acid dihydrazide2-二苯基膦苯甲醛 以75%的产率得到2-ethylmalonic acid 1,3-bis[2-[2-(diphenylphosphino)phenylmethylene]hydrazide]
    参考文献:
    名称:
    Synthesis and characterization of novel bis(diphenylphosphino)-oxalyl and (substituted) malonyl dihydrazones: P,N,N,P-tetradentate complexes of an oxalyl derivative with Cu(II), Pd(II), and Mn(II)
    摘要:
    Novel ligands of bis(diphenylphosphino)-oxalyl, malonyl, and methyl- and ethyl-malonyl dihydrazones were synthesized by condensation of oxalyl, malonyl, methyl-malonyl, and ethyl-malonyl dihydrazide with o-(diphenylphosphino)benzaldehyde in different conditions. The dihydrazones exhibit three different tautomeric structures detected by NMR and IR spectra. The P-31 NMR spectrum demonstrates four different singlet signals, i.e., chemical shifts, of the three respective tautomers. Complexes of the oxalyl ligand with Pd2+, Cu2+, and Mn2+ ions are formed in 1:1 molar ratio. Their structures were characterized by IR, NMR, EPR, MS, EA, and TGA, in which the oxalyl ligand acts as a neutral P,N,N,P-tetradentate chelate. The pH stability of the complexes is in the region of ca. 4.5-7.5 and their activation energy was calculated from the conductivity measurements.
    DOI:
    10.1007/s00706-013-1122-4
  • 作为产物:
    参考文献:
    名称:
    不饱和四和三酯与水合肼和氨基脲的反应
    摘要:
    已分离出各种4,5-二取代的吡唑烷基-3-酮(IIc-f)作为3-取代的四乙基丙烯-1,1,3,3-四羧酸酯(I)与水合肼之间反应的中间体。在反应的3-取代的三乙基丙烯-1,1,3-三羧酸盐(VI)之间,并用水合肼,这给乙基-5-氧代Δ没有获得这样的中间体2 -吡唑啉-4-羧酸叔丁酯(III)和适当的饱和酯(VII)。氨基脲盐酸盐与各种酯类似地反应,得到与水合肼相同的最终产物。
    DOI:
    10.1039/p19720001022
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文献信息

  • Microstructure and mechanical properties of Ti–Si–N coatings
    作者:W. J. Meng、X. D. Zhang、B. Shi、R. C. Tittsworth、L. E. Rehn、P. M. Baldo
    DOI:10.1557/jmr.2002.0381
    日期:2002.10

    A series of Ti–Si–N coatings with 0 < Si < 20 at.% were synthesized by inductively coupled plasma assisted vapor deposition. Coating composition, structure, atomic short-range order, and mechanical response were characterized by Rutherford backscattering spectrometry, transmission electron microscopy, x-ray absorption near-edge structure spectroscopy, and instrumented nanoindentation. These experiments show that the present series of Ti–Si–N coatings consists of a mixture of nanocrystalline titanium nitride (TiN) and amorphous silicon nitride (a-Si:N); i.e., they are TiN/a-Si:N ceramic/ceramic nanocomposites. The hardness of the present series of coatings was found to be less than 32 GPa and to vary smoothly with the Si composition.

    通过电感耦合等离子体辅助气相沉积法合成了一系列 0 < Si < 20 at.% 的 Ti-Si-N 涂层。通过卢瑟福背散射光谱法、透射电子显微镜、X 射线吸收近边结构光谱法和仪器纳米压痕法对涂层的成分、结构、原子短程有序性和机械响应进行了表征。这些实验表明,本系列 Ti-Si-N 涂层由纳米晶氮化钛(TiN)和无定形氮化硅(a-Si:N)的混合物组成,即它们是 TiN/a-Si:N 陶瓷/陶瓷纳米复合材料。研究发现,这一系列涂层的硬度低于 32 GPa,并随硅成分的变化而变化。
  • Curtius, Journal fur praktische Chemie (Leipzig 1954), 1916, vol. <2>94, p. 288
    作者:Curtius
    DOI:——
    日期:——
  • Buelow; Bozenhardt, Chemische Berichte, 1909, vol. 42, p. 4800
    作者:Buelow、Bozenhardt
    DOI:——
    日期:——
  • Braeuniger; Moede, Pharmazie, 1969, vol. 24, # 12, p. 720 - 727
    作者:Braeuniger、Moede
    DOI:——
    日期:——
  • Dornow; Bruncken, Chemische Berichte, 1949, vol. 82, p. 121
    作者:Dornow、Bruncken
    DOI:——
    日期:——
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