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(2S,3S,4S,5R,6S)-4-Benzyloxy-5-hexadecyloxy-2-iodomethyl-6-methoxy-tetrahydro-pyran-3-ol | 878675-44-6

中文名称
——
中文别名
——
英文名称
(2S,3S,4S,5R,6S)-4-Benzyloxy-5-hexadecyloxy-2-iodomethyl-6-methoxy-tetrahydro-pyran-3-ol
英文别名
——
(2S,3S,4S,5R,6S)-4-Benzyloxy-5-hexadecyloxy-2-iodomethyl-6-methoxy-tetrahydro-pyran-3-ol化学式
CAS
878675-44-6
化学式
C30H51IO5
mdl
——
分子量
618.636
InChiKey
CABQJOKZYISQDA-RLXMVLCYSA-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):
    7.61
  • 重原子数:
    36.0
  • 可旋转键数:
    21.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    57.15
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

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
  • 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:
    (2S,3S,4S,5R,6S)-4-Benzyloxy-5-hexadecyloxy-2-iodomethyl-6-methoxy-tetrahydro-pyran-3-ol吡啶 作用下, 以 乙醇二氯甲烷 为溶剂, 反应 6.5h, 生成 (2R,3R,4R)-4-[tert-butyl(dimethyl)silyl]oxy-2-hexadecoxy-3-phenylmethoxyhex-5-enal
    参考文献:
    名称:
    Hydrolytically stable arabinofuranoside analogs for the synthesis of arabinosyltransferase inhibitors
    摘要:
    The first members of two new families of arabinosyltransferase inhibitors, derived from previously reported hybrid compounds covalently associating all iminoalditol with an alpha-D-arabinofuranoside, have been prepared. In place of the arabinofuranoside moiety, they incorporate in their structure a Suitably Substituted tetrahydrofuran (C-glycoside family) or a cyclopentane (carba-sugar family) for mimicking the alpha-D-arabinofuranoside ring. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.12.029
  • 作为产物:
    参考文献:
    名称:
    Hydrolytically stable arabinofuranoside analogs for the synthesis of arabinosyltransferase inhibitors
    摘要:
    The first members of two new families of arabinosyltransferase inhibitors, derived from previously reported hybrid compounds covalently associating all iminoalditol with an alpha-D-arabinofuranoside, have been prepared. In place of the arabinofuranoside moiety, they incorporate in their structure a Suitably Substituted tetrahydrofuran (C-glycoside family) or a cyclopentane (carba-sugar family) for mimicking the alpha-D-arabinofuranoside ring. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2005.12.029
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