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ethoxydimethylfluorosilane | 20502-77-6

中文名称
——
中文别名
——
英文名称
ethoxydimethylfluorosilane
英文别名
Ethoxy(fluoro)dimethylsilane;ethoxy-fluoro-dimethylsilane
ethoxydimethylfluorosilane化学式
CAS
20502-77-6
化学式
C4H11FOSi
mdl
——
分子量
122.215
InChiKey
PRTJBJMHOQZJNW-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

物化性质

  • 沸点:
    58-60 °C(Press: 745 Torr)
  • 密度:
    0.8797 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    1.69
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:a8bd67aa5498c9cf0754a3237aedb616
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反应信息

  • 作为产物:
    描述:
    2-氯乙氧基(二甲基)硅烷 在 caesium fluoride 作用下, 反应 0.5h, 以55.6%的产率得到ethoxydimethylfluorosilane
    参考文献:
    名称:
    Organosilicon and organophosphorus compounds with pseudohalogen groups. 1. Synthesis of alkoxydimethylsilyl cyanides and their reactions with metal fluorides
    摘要:
    Alkoxydimethylsilyl cyanides were synthesized by the exchange reaction of the corresponding alkoxydimethylchlorosilanes with trimethylsilyl cyanide, and also by the reaction of the former compounds with HCN in the presence of triethylamine (the latter method is preferential). Reactions of silyl cyanides with SbF3 and ZnF2 were studied. It was found that the reaction of silyl cyanides with SBF3 leads to the formation of Me2SiF2 and the corresponding alkoxydimethylfluorosilanes, which were also obtained by counter-synthesis from alkoxydimethylsilylchlorosilanes and metal fluorides (SbF3, ZnF2, CsF). Dimethylfluorosilyl cyanide was obtained by the reaction of silyl cyanides with ZnF2.
    DOI:
    10.1007/bf00961242
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文献信息

  • Kochler,P. et al., Zeitschrift fur Chemie, 1977, vol. 17, p. 100 - 101
    作者:Kochler,P. et al.
    DOI:——
    日期:——
  • Organosilicon and organophosphorus compounds with pseudohalogen groups. 1. Synthesis of alkoxydimethylsilyl cyanides and their reactions with metal fluorides
    作者:A. A. Krolevets、V. V. Antipova、I. V. Martynov
    DOI:10.1007/bf00961242
    日期:1991.7
    Alkoxydimethylsilyl cyanides were synthesized by the exchange reaction of the corresponding alkoxydimethylchlorosilanes with trimethylsilyl cyanide, and also by the reaction of the former compounds with HCN in the presence of triethylamine (the latter method is preferential). Reactions of silyl cyanides with SbF3 and ZnF2 were studied. It was found that the reaction of silyl cyanides with SBF3 leads to the formation of Me2SiF2 and the corresponding alkoxydimethylfluorosilanes, which were also obtained by counter-synthesis from alkoxydimethylsilylchlorosilanes and metal fluorides (SbF3, ZnF2, CsF). Dimethylfluorosilyl cyanide was obtained by the reaction of silyl cyanides with ZnF2.
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同类化合物

(2-溴乙氧基)-特丁基二甲基硅烷 骨化醇杂质DCP 马来酸双(三甲硅烷)酯 顺式-二氯二(二甲基硒醚)铂(II) 顺-N-(1-(2-乙氧基乙基)-3-甲基-4-哌啶基)-N-苯基苯酰胺 降钙素杂质13 降冰片烯基乙基三甲氧基硅烷 降冰片烯基乙基-POSS 间-氨基苯基三甲氧基硅烷 镁,氯[[二甲基(1-甲基乙氧基)甲硅烷基]甲基]- 锑,二溴三丁基- 铷,[三(三甲基甲硅烷基)甲基]- 铂(0)-1,3-二乙烯-1,1,3,3-四甲基二硅氧烷 钾(4-{[二甲基(2-甲基-2-丙基)硅烷基]氧基}-1-丁炔-1-基)(三氟)硼酸酯(1-) 金刚烷基乙基三氯硅烷 辛醛,8-[[(1,1-二甲基乙基)二甲基甲硅烷基]氧代]- 辛甲基-1,4-二氧杂-2,3,5,6-四硅杂环己烷 辛基铵甲烷砷酸盐 辛基衍生化硅胶(C8)ZORBAX?LP100/40C8 辛基硅三醇 辛基甲基二乙氧基硅烷 辛基三甲氧基硅烷 辛基三氯硅烷 辛基(三苯基)硅烷 辛乙基三硅氧烷 路易氏剂-3 路易氏剂-2 路易士剂 试剂3-[Tris(trimethylsiloxy)silyl]propylvinylcarbamate 试剂2-(Trimethylsilyl)cyclopent-2-en-1-one 试剂11-Azidoundecyltriethoxysilane 西甲硅油杂质14 衣康酸二(三甲基硅基)酯 苯胺,4-[2-(三乙氧基甲硅烷基)乙基]- 苯磺酸,羟基-,盐,单钠聚合甲醛,1,3,5-三嗪-2,4,6-三胺和脲 苯甲醇,a-[(三苯代甲硅烷基)甲基]- 苯基二甲基氯硅烷 苯基二甲基乙氧基硅 苯基乙酰氧基三甲基硅烷 苯基三辛基硅烷 苯基三甲氧基硅烷 苯基三乙氧基硅烷 苯基三丁酮肟基硅烷 苯基三(异丙烯氧基)硅烷 苯基三(2,2,2-三氟乙氧基)硅烷 苯基(3-氯丙基)二氯硅烷 苯基(1-哌啶基)甲硫酮 苯乙基三苯基硅烷 苯丙基乙基聚甲基硅氧烷 苯-1,3,5-三基三(三甲基硅烷)