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barium α-D-lactopyranosyl-1-phosphate | 103404-65-5

中文名称
——
中文别名
——
英文名称
barium α-D-lactopyranosyl-1-phosphate
英文别名
O4-β-D-Galactopyranosyl-O1-phosphono-α-D-glucopyranose; Barium;alpha-Lactose-1-phosphate barium salt;barium(2+);[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl] phosphate
barium α-D-lactopyranosyl-1-phosphate化学式
CAS
103404-65-5;104808-99-3;107661-83-6
化学式
Ba*C12H21O14P
mdl
——
分子量
557.594
InChiKey
NPJFAEZSRDFUIM-OKVFJUCHSA-L
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):
    -6.92
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    242
  • 氢给体数:
    7
  • 氢受体数:
    14

安全信息

  • 危险品标志:
    Xn
  • 危险类别码:
    R20/21/22
  • WGK Germany:
    3
  • 安全说明:
    S36

SDS

SDS:8b20d0709560b354ab54f1e118a68725
查看

反应信息

  • 作为反应物:
    描述:
    barium α-D-lactopyranosyl-1-phosphate碳酸氢铵 作用下, 以 重水 为溶剂, 生成 α-D-lactopyranosyl-1-phosphate
    参考文献:
    名称:
    Protecting-Group-Free Synthesis of Glycosyl 1–Phosphates
    摘要:
    Glycosyl 1-phosphates enriched in the alpha-anomer are obtained without the use of protecting groups in two steps starting from the free hemiacetal. Condensation of free hemiacetals with toluenesulfonylhydrazide yields a range of glycosylsulfonohydrazide donors which can be oxidized using cupric chloride in the presence of phosphoric acid and the coordinating additive 2-methyl-2-oxazoline to give useful yields of the fully deprotected glycosyl 1-phosphates.
    DOI:
    10.1021/ol3019083
  • 作为产物:
    描述:
    β-乳糖2-甲基-2-恶唑啉磷酸 、 copper dichloride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 18.0h, 生成 barium α-D-lactopyranosyl-1-phosphate
    参考文献:
    名称:
    Protecting-Group-Free Synthesis of Glycosyl 1–Phosphates
    摘要:
    Glycosyl 1-phosphates enriched in the alpha-anomer are obtained without the use of protecting groups in two steps starting from the free hemiacetal. Condensation of free hemiacetals with toluenesulfonylhydrazide yields a range of glycosylsulfonohydrazide donors which can be oxidized using cupric chloride in the presence of phosphoric acid and the coordinating additive 2-methyl-2-oxazoline to give useful yields of the fully deprotected glycosyl 1-phosphates.
    DOI:
    10.1021/ol3019083
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