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1,5-bis(aminooxy)pentane | 444729-87-7

中文名称
——
中文别名
——
英文名称
1,5-bis(aminooxy)pentane
英文别名
O,O'-pentane-1,5-diyl-bis-hydroxylamine;1,5-bis-aminooxy-pentane;1,5-Bis-aminooxy-pentan;O-(5-aminooxypentyl)hydroxylamine
1,5-bis(aminooxy)pentane化学式
CAS
444729-87-7
化学式
C5H14N2O2
mdl
——
分子量
134.178
InChiKey
LRKBNURBAREDAJ-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

  • 沸点:
    132 °C(Press: 15 Torr)
  • 密度:
    1.023±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.5
  • 重原子数:
    9
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    70.5
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1,5-bis(aminooxy)pentaneN,N'-羰基二咪唑 作用下, 反应 1.25h, 生成 2-Amino-N-[5-(2-amino-acetylaminooxy)-pentyloxy]-acetamide; compound with trifluoro-acetic acid
    参考文献:
    名称:
    Johnson; Boxer; Drummond, Arzneimittel-Forschung/Drug Research, 1989, vol. 39, # 4, p. 432 - 437
    摘要:
    DOI:
  • 作为产物:
    描述:
    1,5-Bis-phthalimiidooxy-pentan 在 一水合肼 作用下, 以 乙醇 为溶剂, 生成 1,5-bis(aminooxy)pentane
    参考文献:
    名称:
    Synthesis and Characterization of Methoxy-Substituted Salamo-Type Bisoximes Based on Bis(aminooxy)alkane and 3-Methoxy-2-hydroxybenzaldehyde
    摘要:
    四种新的甲氧基取代的萨拉莫型双肟化合物6,6-二甲氧基-2,2-[(丙烯-1,3-二基二氧基)双(次氮基亚甲基)]联苯酚(H2L1)、6,6-二甲氧基-2、 2-[(丁烯-1,4-二基二氧基)双(次氮基亚甲基)]联苯酚(H2L2)、6,6-二甲氧基-2,2-[(丙烷-1,5-二基二氧基)双(次氮基亚甲基)]联苯酚(HH2L3)和6,6-二甲氧基-2,2-[(己烷-1,6-二基二氧基)双(次氮基亚甲基)]联苯酚(H2L4)分别在热乙醇介质下通过缩合反应合成,并表征为元素分析、红外光谱、紫外-可见光谱和 1H NMR 光谱。
    DOI:
    10.14233/ajchem.2014.17468
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文献信息

  • Synthesis and Dipolymer Structure of Salen-type N2O2 Ligand 2,2'-[(Pentane-1,5-diyldioxy-bis)-bis-(nitrilomethylidyne)]dinaphthalene
    作者:Li Zhao、Yu-Jie Zhang、Shou-Ting Zhang、Hong-Xia Guo、Qian Cheng
    DOI:10.14233/ajchem.2013.14602
    日期:——
    The compound, 2,2-[(pentane-1,5-diyldioxy-bis)-bis-(nitrilomethylidyne)]dinaphthalene has been synthesized by 1,5-bis-(aminooxy)pentane and 2-naphthaldehyde in ethanol solution and characterized structurally by X-ray crystallography. The molecule of the title compound, C27H26N2O2, assumes a dipolymer structure through a weak C-H···C hydrogen-bonding interactions. And the single crystal structure of the compound revealed all-conformation of the (-CH=N-O-(CH2)5-O-N=CH-) linkage, which resulted in the structure with two nitrilomethylidyne units apart from each other. The compound is sufficiently stable to resist scrambling of the C=N bonds. This may be ascribed to lower reactivity of the C=N-O bonds toward nucleophiles.
    2,2-[(pentane-1,5-diyldioxy-bis)-bis-(nitrilomethidyne)]dinaphthalene 这个化合物是由 1,5--bis-(aminooxy)pentane 和 2-naphthaldehyde 在乙醇溶液中合成的,并通过 X 射线晶体学对其结构进行了表征。标题化合物 C27H26N2O2 的分子通过微弱的 C-H-C 氢键作用形成二聚体结构。该化合物的单晶结构显示了(-CH=N-O-(CH2)5-O-N=CH-)连接的全构象,从而形成了两个相距较远的氮甲基单元的结构。该化合物具有足够的稳定性,可以抵御 C=N 键的破坏。这可能是因为 C=N-O 键对亲核物的反应性较低。
  • Synthesis and Characterization of Five Bisoxime-Type Chelating Ligands Based on Bis(aminooxy)alkane and 2-Naphthaldehyde
    作者:Gang Li、Su-Xia Gao、Zong-Li Ren、Na We、Li Wang、Xiu-Yan Dong
    DOI:10.14233/ajchem.2014.17492
    日期:——
    Five bisoxime chelating ligands L1-L5 have been synthesized from 2-naphthaldehyde and 1,2-bis(aminooxy)ethane, 1,3-bis(aminooxy)-propane, 1,4-bis(aminooxy)butane, 1,5-bis(aminooxy)pentane and 1,6-bis(aminooxy)hexane in hot ethanolic medium, respectively and characterized by elemental analyses, IR, UV-visible spectra and 1H NMR spectroscopy. The bisoxime chelating ligands L1-L5 may be promising units for the construction of supramolecular metal complexes.
    在热乙醇介质中,以 2-萘甲醛和 1,2-双(氨基氧)乙烷、1,3-双(氨基氧)丙烷、1,4-双(氨基氧)丁烷、1,5-双(氨基氧)戊烷和 1,6-双(氨基氧)己烷为原料,分别合成了五种双肟螯合配体 L1-L5,并通过元素分析、红外光谱、紫外可见光谱和 1H NMR 光谱对其进行了表征。双肟螯合配体 L1-L5 可能是构建超分子金属配合物的有前途的单元。
  • Synthesis and Characterization of Nitro Salamo-Type Bisoxime Compounds
    作者:Gang Li、Li Wang、Yu-Hua Yang、Meng-Meng Zhao、Yu-Jie Zhang
    DOI:10.14233/ajchem.2013.15445
    日期:——
    A series of nitro salamo-type bisoxime compounds have been synthesized from 2-hydroxy-5-nitrobenzaldehyde and 1,2-bis(aminooxy)-ethane, 1,3-bis(aminooxy)propane, 1,4-bis(aminooxy)butane or 1,5-bis(aminooxy)pentane in ethanol medium, respectively and characterized by elemental analyses as well as IR, UV-visible and 1H NMR spectroscopy.
    在乙醇介质中,以 2-hydroxy-5-nitrobenzaldehyde 和 1,2-bis(aminooxy)-ethane、1,3-bis(aminooxy)propane、1,4-bis(aminooxy)butane 或 1,5-bis(aminooxy)pentane 为原料,分别合成了一系列硝基水杨酸类双肟化合物,并通过元素分析以及红外光谱、紫外可见光谱和 1H NMR 光谱进行了表征。
  • Synthesis and Characterization of Bromo-Substituted Salamo-Type Bisoxime Compounds Series
    作者:Li Xu、Na Li、Yang Zhang、Na Wen、Li-Chun Zhu、Xiu-Yan Dong
    DOI:10.14233/ajchem.2014.17398
    日期:——
    Four novel bromo-substituted Salamo-type bisoxime compounds H2L1-H2L4 have been synthesized from 5-bromo-2-hydroxybenzaldehyde and 1,3-bis(aminooxy)propane, 1,4-bis(aminooxy)butane, 1,5-bis(aminooxy)pentane or 1,6-bis(aminooxy)henane in hot ethanolic medium, respectively and characterized by elemental analyses, IR, UV-visible spectra and 1H NMR spectroscopy.
    以5-溴-2-羟基苯甲醛和1,3-双(氨氧基)丙烷、1,4-双(氨氧基)丁烷、1,5-双为原料合成了四种新型溴取代Salamo型双肟化合物H2L1-H2L4分别在热乙醇介质中的(氨基氧基)戊烷或 1,6-双(氨基氧基)己烷,并通过元素分析、红外、紫外-可见光谱和 1H NMR 光谱进行表征。
  • Synthesis and Characterization of Methoxy-Substituted Salamo-Type Bisoximes Based on Bis(aminooxy)alkane and 3-Methoxy-2-hydroxybenzaldehyde
    作者:Zong-Li Ren、Su-Xia Gao、Yang Zhang、Li Wang、Xiu-Yan Dong
    DOI:10.14233/ajchem.2014.17468
    日期:——
    Four new methoxy-substituted Salamo-type bisoxime compounds 6,6-dimethoxy-2,2-[(propylene-1,3-diyldioxy)bis(nitrilo-methylidyne)]diphenol (H2L1), 6,6-dimethoxy-2,2-[(butylene-1,4-diyldioxy)bis(nitrilomethylidyne)]diphenol (H2L2), 6,6-dimethoxy-2,2-[(propane-1,5-diyldioxy)bis(nitrilome-thylidyne)]diphenol (HH2L3) and 6,6-dimethoxy-2,2-[(hexane-1,6-diyldioxy)bis(nitrilo-methylidyne)]diphenol (H2L4) have been synthesized through condensation reactions under hot ethanol medium, respectively and characterized by elemental analyses, IR, UV-visible and 1H NMR spectra.
    四种新的甲氧基取代的萨拉莫型双肟化合物6,6-二甲氧基-2,2-[(丙烯-1,3-二基二氧基)双(次氮基亚甲基)]联苯酚(H2L1)、6,6-二甲氧基-2、 2-[(丁烯-1,4-二基二氧基)双(次氮基亚甲基)]联苯酚(H2L2)、6,6-二甲氧基-2,2-[(丙烷-1,5-二基二氧基)双(次氮基亚甲基)]联苯酚(HH2L3)和6,6-二甲氧基-2,2-[(己烷-1,6-二基二氧基)双(次氮基亚甲基)]联苯酚(H2L4)分别在热乙醇介质下通过缩合反应合成,并表征为元素分析、红外光谱、紫外-可见光谱和 1H NMR 光谱。
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