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(5R,6R,14R,15R)-6,14-dibutyl-7,10,13-trioxanonadecane-5,15-diol | 623948-07-2

中文名称
——
中文别名
——
英文名称
(5R,6R,14R,15R)-6,14-dibutyl-7,10,13-trioxanonadecane-5,15-diol
英文别名
(5R,6R)-6-[2-[2-[(5R,6R)-6-hydroxydecan-5-yl]oxyethoxy]ethoxy]decan-5-ol
(5R,6R,14R,15R)-6,14-dibutyl-7,10,13-trioxanonadecane-5,15-diol化学式
CAS
623948-07-2
化学式
C24H50O5
mdl
——
分子量
418.658
InChiKey
KRYPGESAXWQPSA-MOUTVQLLSA-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):
    5.9
  • 重原子数:
    29
  • 可旋转键数:
    22
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    68.2
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    (5R,6R,14R,15R)-6,14-dibutyl-7,10,13-trioxanonadecane-5,15-diol 在 palladium on activated charcoal 氢气 、 sodium hydride 作用下, 以 四氢呋喃乙醇 为溶剂, 生成 (4R,5R,13R,14R)-4,5,13,14-tetrabutyl-3,6,9,12,15-pentaoxa-21-azabicyclo-[15.3.1]heneicosa-17,20-diene-19(21H)-one
    参考文献:
    名称:
    Synthesis of new optically active pyridino- and pyridono-18-crown-6 type ligands containing four lipophilic chains
    摘要:
    Highly lipophilic enantiomerically pure pyridino- and pyridono-18-crown-6 type ligands containing four stereogenic centers to which butyl or butoxymethyl groups are attached have been synthesized. X-Ray analysis of the (R)-1-phenylethylammonium and benzylammonium perchlorate complexes of the unsubstituted pyridono ligand revealed, that, in contrast to the free ligand, in the complex the hydroxypyridine tautomer is present. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0957-4166(03)00590-1
  • 作为产物:
    描述:
    (5R,6R)-decane-5,6-diol 在 palladium on activated charcoal 氢气 、 sodium hydride 、 二异丁基氢化铝对甲苯磺酸 作用下, 以 四氢呋喃乙醇二氯甲烷N,N-二甲基甲酰胺甲苯 为溶剂, 反应 1.25h, 生成 (5R,6R,14R,15R)-6,14-dibutyl-7,10,13-trioxanonadecane-5,15-diol
    参考文献:
    名称:
    Synthesis of new optically active pyridino- and pyridono-18-crown-6 type ligands containing four lipophilic chains
    摘要:
    Highly lipophilic enantiomerically pure pyridino- and pyridono-18-crown-6 type ligands containing four stereogenic centers to which butyl or butoxymethyl groups are attached have been synthesized. X-Ray analysis of the (R)-1-phenylethylammonium and benzylammonium perchlorate complexes of the unsubstituted pyridono ligand revealed, that, in contrast to the free ligand, in the complex the hydroxypyridine tautomer is present. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0957-4166(03)00590-1
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文献信息

  • Synthesis of new optically active pyridino- and pyridono-18-crown-6 type ligands containing four lipophilic chains
    作者:János Gerencsér、Nikoletta Báthori、Mátyás Czugler、Péter Huszthy、Mihály Nógrádi
    DOI:10.1016/s0957-4166(03)00590-1
    日期:2003.9
    Highly lipophilic enantiomerically pure pyridino- and pyridono-18-crown-6 type ligands containing four stereogenic centers to which butyl or butoxymethyl groups are attached have been synthesized. X-Ray analysis of the (R)-1-phenylethylammonium and benzylammonium perchlorate complexes of the unsubstituted pyridono ligand revealed, that, in contrast to the free ligand, in the complex the hydroxypyridine tautomer is present. (C) 2003 Elsevier Ltd. All rights reserved.
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