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2-(2-呋喃基亚甲基氨基)乙酸 | 375365-51-8

中文名称
2-(2-呋喃基亚甲基氨基)乙酸
中文别名
——
英文名称
{[1-Furan-2-yl-meth-(E)-ylidene]-amino}-acetic acid
英文别名
Glycine, N-(2-furanylmethylene)-;2-(furan-2-ylmethylideneamino)acetic acid
2-(2-呋喃基亚甲基氨基)乙酸化学式
CAS
375365-51-8
化学式
C7H7NO3
mdl
——
分子量
153.137
InChiKey
HBKWGWXLBXMSTG-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):
    0.7
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    62.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    二乙氧基二甲基硅烷2-(2-呋喃基亚甲基氨基)乙酸 为溶剂, 生成 [[2-(Furan-2-ylmethylideneamino)acetyl]oxy-dimethylsilyl] 2-(furan-2-ylmethylideneamino)acetate
    参考文献:
    名称:
    COORDINATION BEHAVIOR OF BIOLOGICALLY ACTIVE SCHIFF BASES OF AMINO ACIDS TOWARDS SILICON(IV) ION
    摘要:
    Reactions of diethoxydimethylsilane with Schiff bases derived from the condensation of fur-furaldehyde, indole-3-carbaldehyde with alanine, glycine, valine, isoleucine and tryptophan in a 1:2 molar ratio give a new series of Me2Si ((N O) over cap)(2) type of organosilicon (IV) complexes. The complexes are monomeric and non-electrolytic in nature. The coordination behaviour of Schiff bases through organosilicon (IV) has been investigated by IR, H-1, C-13 & Si-29 NMR spectral studies. Schiff bases and their silicon complexes have also been screened for their antifungal activity. Several of these complexes were found to be quite active in this respect.
    DOI:
    10.1080/10426500108040248
  • 作为产物:
    描述:
    糠醛聚甘氨酸乙醇 为溶剂, 反应 5.0h, 生成 2-(2-呋喃基亚甲基氨基)乙酸
    参考文献:
    名称:
    COORDINATION BEHAVIOR OF BIOLOGICALLY ACTIVE SCHIFF BASES OF AMINO ACIDS TOWARDS SILICON(IV) ION
    摘要:
    Reactions of diethoxydimethylsilane with Schiff bases derived from the condensation of fur-furaldehyde, indole-3-carbaldehyde with alanine, glycine, valine, isoleucine and tryptophan in a 1:2 molar ratio give a new series of Me2Si ((N O) over cap)(2) type of organosilicon (IV) complexes. The complexes are monomeric and non-electrolytic in nature. The coordination behaviour of Schiff bases through organosilicon (IV) has been investigated by IR, H-1, C-13 & Si-29 NMR spectral studies. Schiff bases and their silicon complexes have also been screened for their antifungal activity. Several of these complexes were found to be quite active in this respect.
    DOI:
    10.1080/10426500108040248
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文献信息

  • Shukla, P. R.; Pandey, O. P.; Narain, Gopal, Journal of the Indian Chemical Society, <hi>1983</hi>, vol. 60, p. 397 - 399
    作者:Shukla, P. R.、Pandey, O. P.、Narain, Gopal
    DOI:——
    日期:——
  • COORDINATION BEHAVIOR OF BIOLOGICALLY ACTIVE SCHIFF BASES OF AMINO ACIDS TOWARDS SILICON(IV) ION
    作者:M. Sharma、B. Khungar、S. Varshney、H. L. Singh、U. D. Tripaathi、A. K. Varshney
    DOI:10.1080/10426500108040248
    日期:2001.8.1
    Reactions of diethoxydimethylsilane with Schiff bases derived from the condensation of fur-furaldehyde, indole-3-carbaldehyde with alanine, glycine, valine, isoleucine and tryptophan in a 1:2 molar ratio give a new series of Me2Si ((N O) over cap)(2) type of organosilicon (IV) complexes. The complexes are monomeric and non-electrolytic in nature. The coordination behaviour of Schiff bases through organosilicon (IV) has been investigated by IR, H-1, C-13 & Si-29 NMR spectral studies. Schiff bases and their silicon complexes have also been screened for their antifungal activity. Several of these complexes were found to be quite active in this respect.
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