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(8-Hydroxymethyl-3,6-dimethoxy-naphthalen-1-yl)-methanol | 159434-54-5

中文名称
——
中文别名
——
英文名称
(8-Hydroxymethyl-3,6-dimethoxy-naphthalen-1-yl)-methanol
英文别名
[8-(Hydroxymethyl)-3,6-dimethoxynaphthalen-1-yl]methanol
(8-Hydroxymethyl-3,6-dimethoxy-naphthalen-1-yl)-methanol化学式
CAS
159434-54-5
化学式
C14H16O4
mdl
——
分子量
248.279
InChiKey
QGWONEVFCOODES-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):
    1.3
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    58.9
  • 氢给体数:
    2
  • 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:
    (8-Hydroxymethyl-3,6-dimethoxy-naphthalen-1-yl)-methanol吡啶chromium(VI) oxide4-二甲氨基吡啶双[Α,Α-双(三氟甲基)苯甲醇合]二苯硫二甲基硫乙醇硫酸sodium methylate三溴化磷lithium 、 sodium hydride 、 对甲苯磺酸臭氧三乙胺 、 lithium bromide 作用下, 以 四氢呋喃甲醇乙醚二氯甲烷溶剂黄146丙酮 为溶剂, 反应 26.0h, 生成 Methanesulfonic acid 5,8-bis-methanesulfonyloxy-dodecahydro-phenalen-2-yl ester
    参考文献:
    名称:
    Conformationally Rigid Tricyclic Tripods: Synthesis and Application to Preparation of Enterobactin Analogs
    摘要:
    The syntheses of the conformationally rigid triol 2 and triamine 3 are described. One of the key features of these syntheses was that each of the intermediates involved contained a symmetry element, which made their structure elucidation facile and conclusive. The structural similarity between the platform of enterobactin in its metal binding state and triamine 3 was recognized, and the enterobactin analog 14 was synthesized. The K-f value observed for 14 was as high as the K-f value for enterobactin itself, and higher than the K-f value for any enterobactin analog ever reported. In comparison with a number of synthetic enterobactin analogs, it became evident that the conformational rigidity of the enterobactin platform, resulting in good preorganization of the three catechol moieties toward Fe(III)-chelation, was an important factor contributing to its extraordinarily high K-f.
    DOI:
    10.1021/jo00104a043
  • 作为产物:
    参考文献:
    名称:
    Conformationally Rigid Tricyclic Tripods: Synthesis and Application to Preparation of Enterobactin Analogs
    摘要:
    The syntheses of the conformationally rigid triol 2 and triamine 3 are described. One of the key features of these syntheses was that each of the intermediates involved contained a symmetry element, which made their structure elucidation facile and conclusive. The structural similarity between the platform of enterobactin in its metal binding state and triamine 3 was recognized, and the enterobactin analog 14 was synthesized. The K-f value observed for 14 was as high as the K-f value for enterobactin itself, and higher than the K-f value for any enterobactin analog ever reported. In comparison with a number of synthetic enterobactin analogs, it became evident that the conformational rigidity of the enterobactin platform, resulting in good preorganization of the three catechol moieties toward Fe(III)-chelation, was an important factor contributing to its extraordinarily high K-f.
    DOI:
    10.1021/jo00104a043
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文献信息

  • Conformationally Rigid Tricyclic Tripods: Synthesis and Application to Preparation of Enterobactin Analogs
    作者:Bruno Tse、Yoshito Kishi
    DOI:10.1021/jo00104a043
    日期:1994.12
    The syntheses of the conformationally rigid triol 2 and triamine 3 are described. One of the key features of these syntheses was that each of the intermediates involved contained a symmetry element, which made their structure elucidation facile and conclusive. The structural similarity between the platform of enterobactin in its metal binding state and triamine 3 was recognized, and the enterobactin analog 14 was synthesized. The K-f value observed for 14 was as high as the K-f value for enterobactin itself, and higher than the K-f value for any enterobactin analog ever reported. In comparison with a number of synthetic enterobactin analogs, it became evident that the conformational rigidity of the enterobactin platform, resulting in good preorganization of the three catechol moieties toward Fe(III)-chelation, was an important factor contributing to its extraordinarily high K-f.
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