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4-[(R)-((4S,5S)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-methoxy-methyl]-hepta-1,6-dien-4-ol | 264891-33-0

中文名称
——
中文别名
——
英文名称
4-[(R)-((4S,5S)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-methoxy-methyl]-hepta-1,6-dien-4-ol
英文别名
4-[(R)-[(4S,5S)-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]-methoxymethyl]hepta-1,6-dien-4-ol
4-[(R)-((4S,5S)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-methoxy-methyl]-hepta-1,6-dien-4-ol化学式
CAS
264891-33-0
化学式
C15H26O5
mdl
——
分子量
286.368
InChiKey
HUMSUFUKSOMQOU-RWMBFGLXSA-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):
    1.2
  • 重原子数:
    20
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.73
  • 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:
    参考文献:
    名称:
    Stereoselective synthesis of 5-monoalkyl and 5,5-dialkylsubstituted noviose derivatives
    摘要:
    fThe stereoselective synthesis of 5-monosubstituted and 5,5-dialkylsubstituted noviose derivatives has been achieved starting from L-arabinose. These noviose derivatives could be used as useful building blocks in probing structure-activity relationships (SAR) of coumarin antibiotics that are inhibitors of DNA gyrase. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(99)02177-2
  • 作为产物:
    描述:
    (3aS,7R,7aS)-7-Methoxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-one烯丙基溴化镁四氢呋喃 为溶剂, 以50%的产率得到4-[(R)-((4S,5S)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-methoxy-methyl]-hepta-1,6-dien-4-ol
    参考文献:
    名称:
    Stereoselective synthesis of 5-monoalkyl and 5,5-dialkylsubstituted noviose derivatives
    摘要:
    fThe stereoselective synthesis of 5-monosubstituted and 5,5-dialkylsubstituted noviose derivatives has been achieved starting from L-arabinose. These noviose derivatives could be used as useful building blocks in probing structure-activity relationships (SAR) of coumarin antibiotics that are inhibitors of DNA gyrase. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(99)02177-2
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