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(3aR,5R,6R,7S,7aS)-2-azidomethyl-7-benzyloxy-5-hydroxymethyl-hexahydro-furo[3,2-b]pyran-6-ol | 776313-94-1

中文名称
——
中文别名
——
英文名称
(3aR,5R,6R,7S,7aS)-2-azidomethyl-7-benzyloxy-5-hydroxymethyl-hexahydro-furo[3,2-b]pyran-6-ol
英文别名
——
(3aR,5R,6R,7S,7aS)-2-azidomethyl-7-benzyloxy-5-hydroxymethyl-hexahydro-furo[3,2-b]pyran-6-ol化学式
CAS
776313-94-1
化学式
C16H21N3O5
mdl
——
分子量
335.36
InChiKey
YCYZQJMZFQURTL-WCJVTGSSSA-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):
    1.16
  • 重原子数:
    24.0
  • 可旋转键数:
    6.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    116.91
  • 氢给体数:
    2.0
  • 氢受体数:
    6.0

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:
    (3aR,5R,6R,7S,7aS)-2-azidomethyl-7-benzyloxy-5-hydroxymethyl-hexahydro-furo[3,2-b]pyran-6-ol异氰-3-氟基苯酯环丙甲酸 以5.8 mg的产率得到cyclopropanecarboxylic acid (3aR,5R,6R,7R,7aS)-7-benzyloxy-2-[3-(3-fluoro-phenyl)-ureidomethyl]-5-hydroxymethyl-hexahydro-furo[3,2-b]pyran-6-yl ester
    参考文献:
    名称:
    Bicyclic carbohydrate-derived scaffolds for combinatorial libraries
    摘要:
    A bicyclic scaffold derived from the natural monosaccharide D-glucose, and possessing several diversity sites, was linked to various resins through the primary (C-6) hydroxyl and decorated on the solid phase: the hydroxyl group at C-4 was functionalized as ester, ether, and carbamate, the amino group ill the second cycle (C-3' position) was functionalized as amide, sulfonamide, and ureido- and thioureido-derivatives. The compounds synthesized oil the solid phase were tested for their antiproliferative activity oil tumor cell lines. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2005.12.055
  • 作为产物:
    参考文献:
    名称:
    Bicyclic carbohydrate-derived scaffolds for combinatorial libraries
    摘要:
    A bicyclic scaffold derived from the natural monosaccharide D-glucose, and possessing several diversity sites, was linked to various resins through the primary (C-6) hydroxyl and decorated on the solid phase: the hydroxyl group at C-4 was functionalized as ester, ether, and carbamate, the amino group ill the second cycle (C-3' position) was functionalized as amide, sulfonamide, and ureido- and thioureido-derivatives. The compounds synthesized oil the solid phase were tested for their antiproliferative activity oil tumor cell lines. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2005.12.055
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