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2-[D3]Methoxy-4-(tetrahydropyran-2-yloxymethyl)phenol | 347894-36-4

中文名称
——
中文别名
——
英文名称
2-[D3]Methoxy-4-(tetrahydropyran-2-yloxymethyl)phenol
英文别名
4-(Oxan-2-yloxymethyl)-2-(trideuteriomethoxy)phenol;4-(oxan-2-yloxymethyl)-2-(trideuteriomethoxy)phenol
2-[D3]Methoxy-4-(tetrahydropyran-2-yloxymethyl)phenol化学式
CAS
347894-36-4
化学式
C13H18O4
mdl
——
分子量
241.26
InChiKey
YYYKXBSTQZFURD-FIBGUPNXSA-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):
    2
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    47.9
  • 氢给体数:
    1
  • 氢受体数:
    4

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
  • 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:
    2-[D3]Methoxy-4-(tetrahydropyran-2-yloxymethyl)phenol甲酸4-甲基苯磺酸吡啶potassium carbonatecaesium carbonate 、 sodium iodide 作用下, 以 乙醇氯仿N,N-二甲基甲酰胺丙酮 为溶剂, 反应 44.0h, 生成
    参考文献:
    名称:
    Synthesis of Deuterium-Labeled Cryptophane-A and Investigation of Xe@Cryptophane Complexation Dynamics by 1D-EXSY NMR Experiments
    摘要:
    We present the synthesis of a series of deuterated cryptophanes 2-6 by a slightly modified procedure used for cryptophane-A. We show that for [Xe@cryptophane] complexes the use of variable-temperature one-dimensional 129Xe magnetization transfer (1D-EX-SY) allows the measurement of exchange rates. From these data the decomplexation activation energy Ea has been estimated to be 37.5+/-2 kJ mol(-1). The decomplexation activation enthalpy, deltaH(++) = 35.5+/-2 kJ mol(-1), and entropy, deltaS(++) = -60+/-5 J mol(-1) K(-1), have also been calculated. The calculated negative activation entropy suggests that the activated complex associated with decomplexation is conformationally more strained than the complex in its ground state.
    DOI:
    10.1002/1521-3765(20010401)7:7<1561::aid-chem1561>3.0.co;2-9
  • 作为产物:
    描述:
    4-(allyloxy)-3-hydroxybenzaldehyde 在 palladium diacetate 、 sodium tetrahydroborate 、 4-甲基苯磺酸吡啶potassium carbonate二乙胺三苯基膦 作用下, 以 四氢呋喃甲醇二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 生成 2-[D3]Methoxy-4-(tetrahydropyran-2-yloxymethyl)phenol
    参考文献:
    名称:
    Synthesis of Deuterium-Labeled Cryptophane-A and Investigation of Xe@Cryptophane Complexation Dynamics by 1D-EXSY NMR Experiments
    摘要:
    We present the synthesis of a series of deuterated cryptophanes 2-6 by a slightly modified procedure used for cryptophane-A. We show that for [Xe@cryptophane] complexes the use of variable-temperature one-dimensional 129Xe magnetization transfer (1D-EX-SY) allows the measurement of exchange rates. From these data the decomplexation activation energy Ea has been estimated to be 37.5+/-2 kJ mol(-1). The decomplexation activation enthalpy, deltaH(++) = 35.5+/-2 kJ mol(-1), and entropy, deltaS(++) = -60+/-5 J mol(-1) K(-1), have also been calculated. The calculated negative activation entropy suggests that the activated complex associated with decomplexation is conformationally more strained than the complex in its ground state.
    DOI:
    10.1002/1521-3765(20010401)7:7<1561::aid-chem1561>3.0.co;2-9
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文献信息

  • Synthesis of Deuterium-Labeled Cryptophane-A and Investigation of Xe@Cryptophane Complexation Dynamics by 1D-EXSY NMR Experiments
    作者:Thierry Brotin、Thomas Devic、Anne Lesage、Lyndon Emsley、André Collet
    DOI:10.1002/1521-3765(20010401)7:7<1561::aid-chem1561>3.0.co;2-9
    日期:2001.4.1
    We present the synthesis of a series of deuterated cryptophanes 2-6 by a slightly modified procedure used for cryptophane-A. We show that for [Xe@cryptophane] complexes the use of variable-temperature one-dimensional 129Xe magnetization transfer (1D-EX-SY) allows the measurement of exchange rates. From these data the decomplexation activation energy Ea has been estimated to be 37.5+/-2 kJ mol(-1). The decomplexation activation enthalpy, deltaH(++) = 35.5+/-2 kJ mol(-1), and entropy, deltaS(++) = -60+/-5 J mol(-1) K(-1), have also been calculated. The calculated negative activation entropy suggests that the activated complex associated with decomplexation is conformationally more strained than the complex in its ground state.
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