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Silane, (iodomethyl)dimethylpropyl-

中文名称
——
中文别名
——
英文名称
Silane, (iodomethyl)dimethylpropyl-
英文别名
iodomethyl-dimethyl-propylsilane
Silane, (iodomethyl)dimethylpropyl-化学式
CAS
——
化学式
C6H15ISi
mdl
——
分子量
242.175
InChiKey
NQRKKHGWHOEHMI-UHFFFAOYSA-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):
    3.08
  • 重原子数:
    8
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    Silane, (iodomethyl)dimethylpropyl- 在 palladium on activated charcoal 甲醇甲酸三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 (2R,3R,4R,5S)-1-(Dimethyl-propyl-silanylmethyl)-2-hydroxymethyl-piperidine-3,4,5-triol
    参考文献:
    名称:
    New deoxynojirimycin derivatives as potent inhibitors of intestinal α-glucohydrolases
    摘要:
    New N-alkyl, alkenyl and benzyl substituted DNJ derivatives incorporating a silicon atom in the substituent were synthesised. Kinetic parameters (K-i, t(1/2)) for inhibition of rat intestinal alpha-glucohydrolases as well as human lysosomal alpha-glucosidases were measured. New DNJ derivatives are potent and selective inhibitors of intestinal alpha-glucohydrolases. (C) 1997, Elsevier Science Ltd.
    DOI:
    10.1016/s0960-894x(97)00012-7
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文献信息

  • Foeldeak, Sandor; Molnar, Maria; Lokoes, Magdalena, Liebigs Annalen der Chemie, 1994, # 2, p. 211 - 212
    作者:Foeldeak, Sandor、Molnar, Maria、Lokoes, Magdalena
    DOI:——
    日期:——
  • New deoxynojirimycin derivatives as potent inhibitors of intestinal α-glucohydrolases
    作者:Brigitte Lesur、Jean-Bernard Ducep、Marie-Noelle Lalloz、Anne Ehrhard、Charles Danzin
    DOI:10.1016/s0960-894x(97)00012-7
    日期:1997.2
    New N-alkyl, alkenyl and benzyl substituted DNJ derivatives incorporating a silicon atom in the substituent were synthesised. Kinetic parameters (K-i, t(1/2)) for inhibition of rat intestinal alpha-glucohydrolases as well as human lysosomal alpha-glucosidases were measured. New DNJ derivatives are potent and selective inhibitors of intestinal alpha-glucohydrolases. (C) 1997, Elsevier Science Ltd.
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