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N-tosyl-bis(3-iodopropyl)amine | 1326626-44-1

中文名称
——
中文别名
——
英文名称
N-tosyl-bis(3-iodopropyl)amine
英文别名
N-tosylbis(3-iodopropyl)amine
N-tosyl-bis(3-iodopropyl)amine化学式
CAS
1326626-44-1
化学式
C13H19I2NO2S
mdl
——
分子量
507.174
InChiKey
HLJNNYDEZJGQII-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):
    3.64
  • 重原子数:
    19.0
  • 可旋转键数:
    8.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    37.38
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

上下游信息

  • 上游原料
    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:
    N-tosyl-bis(3-iodopropyl)amine 在 lithium aluminium tetrahydride 、 caesium carbonate 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 102.0h, 生成 1,9-diaza-5,13-dithiocyclohexadecane
    参考文献:
    名称:
    Synthesis and characterisation of new porphyrazinato magnesium containing macrobicyclic moieties
    摘要:
    Novel porphyrazinato magnesium (MgPz) containing symmetrically four diaza-tetrathia-macrobicycles on peripheral positions was synthesized by the cyclotetramerisation reaction of 5,8,16,23-tetrathia-1,12-diazabicyclo[9.7.7]pentacosane-6-en-6,7-dicarbodinitril (9), which was prepared by sequence reaction of N-tosyl-bis[3-bis(tosyloxypropyl)] amine (1) and disodium cis-1,2-dicyano-1,2-ethylenedithiolate (8). Elemental analysis, IR, NMR, MS and UV-vis data confirmed the ability of bulky cryptand moieties to induce steric isolation of Pz core in the solid state.
    DOI:
    10.1080/10610278.2011.575468
  • 作为产物:
    描述:
    bis(3-tosyloxypropyl)tosylamine 在 sodium iodide 作用下, 以 丙酮 为溶剂, 反应 3.0h, 以81.1%的产率得到N-tosyl-bis(3-iodopropyl)amine
    参考文献:
    名称:
    Synthesis and characterisation of new porphyrazinato magnesium containing macrobicyclic moieties
    摘要:
    Novel porphyrazinato magnesium (MgPz) containing symmetrically four diaza-tetrathia-macrobicycles on peripheral positions was synthesized by the cyclotetramerisation reaction of 5,8,16,23-tetrathia-1,12-diazabicyclo[9.7.7]pentacosane-6-en-6,7-dicarbodinitril (9), which was prepared by sequence reaction of N-tosyl-bis[3-bis(tosyloxypropyl)] amine (1) and disodium cis-1,2-dicyano-1,2-ethylenedithiolate (8). Elemental analysis, IR, NMR, MS and UV-vis data confirmed the ability of bulky cryptand moieties to induce steric isolation of Pz core in the solid state.
    DOI:
    10.1080/10610278.2011.575468
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文献信息

  • Synthesis and characterization of metal-free phthalocyanine containing 16-membered N2S2-donor macrocycles linked to a 2-pyridinyl methyl moiety
    作者:Nilgün Kabay、Yaşar Gök
    DOI:10.1016/j.tetlet.2013.05.125
    日期:2013.7
    A metal-free phthalocyanine (H2Pc) containing four diazadithiamacrocycles a with 2-pyridinyl methyl groups attached was synthesized via cyclotetramerization of 4,5-bis2-[13(2-pyridinylmethyl)-1,9-dithia-5,13-diazacyclohexadecanyl-5]ethyl} thiophthalonitrile in the presence of DBU as a strong organic base. New compounds were characterized by a combination of elemental analysis, 1H NMR, 13C NMR, IR
    通过4,5-双2- [13-(2-吡啶基甲基)-1,9-dithia-5,]的环四聚反应合成了包含四个带有2-吡啶基甲基的重氮二氮杂大环a的无酞菁(H 2 Pc)。在作为强有机碱的DBU存在下的13-二氮环六癸基-5]乙基}代邻苯二甲腈。新化合物通过元素分析,1 H NMR,13 C NMR,IR,UV / vis和MS光谱数据的组合进行表征。
  • Synthesis and characterization of a new zinc phthalocyanine containing macrobicyclic moieties
    作者:Nuray Demirayak、Fatma Akkuş、Yaşar Gök
    DOI:10.1016/j.inoche.2013.09.050
    日期:2013.11
    Novel zinc phthalocyanine (ZnPc) containing symmetrically eight triaza-tetraoxa macrobicycles on peripheral positions has been synthesized in a multistep reaction sequence. The cyclotetramerization reaction was accomplished with 4,5-bis[2-(4,7,13,16-tetraoxa-1,10,22-triazabicyclo[8.8.7]pentacosane-22-yl)ethylthiolphthalonitrile (6) which was prepared by the reaction of 12-bis(2-iodoethoxy)-4,5-dicyanobenzene (5) and 4.7,13,16-tetraoxa-1,10,22-triazabicyclo[8.8.7]pentacosane (4). The novel compounds were characterized by a combination of elemental analysis, H-1 and C-13 NMR, IR, UV-vis and MS spectral data. (C) 2013 Elsevier B.V. All rights reserved.
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