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methoxydimethylsilyl cyanide | 23272-12-0

中文名称
——
中文别名
——
英文名称
methoxydimethylsilyl cyanide
英文别名
[methoxy(dimethyl)silyl]formonitrile
methoxydimethylsilyl cyanide化学式
CAS
23272-12-0
化学式
C4H9NOSi
mdl
——
分子量
115.207
InChiKey
QCTXGOKPKPFAEO-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:
    56 °C(Press: 60 Torr)
  • 密度:
    0.8851 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    7
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    33
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:16196626f34c9b1685f1d1b59a1f5fc7
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反应信息

  • 作为反应物:
    描述:
    methoxydimethylsilyl cyanide三氯化磷 以 neat (no solvent) 为溶剂, 以96.7%的产率得到二氰基膦基氢氰酸
    参考文献:
    名称:
    Organosilicon and organophosphorus compounds with pseudohalide groups. 2. Reactions of alkoxydimethylsilyl cyanides with chlorides of tricoordinated phosphorus
    摘要:
    Reactions of alkoxydimethylsilyl cyanides with some chlorides of tricoordinated phosphorus ("phosphorous chlorides") have been studied. It is shown that, depending on the nature of the phosphorous chloride, the chlorine atoms can either be substituted only for cyano groups, or for alkoxy and cyano groups simultaneously. The results obtained in this work clearly show that alkoxydimethylsilyl cyanides are more reactive reagents for attaching cyano groups to a phosphorus atom than trimethylsilyl cyanide.
    DOI:
    10.1007/bf00959728
  • 作为产物:
    描述:
    氢氰酸二甲基甲氧基氯硅烷三乙胺 作用下, 以 乙醚 为溶剂, 反应 5.0h, 以70.3%的产率得到methoxydimethylsilyl cyanide
    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

  • Krolevets, A. A.; Martynov, I. V., Journal of general chemistry of the USSR, 1991, vol. 61, # 1.2, p. 236
    作者:Krolevets, A. A.、Martynov, I. V.
    DOI:——
    日期:——
  • Organosilicon and organophosphorus compounds with pseudohalide groups
    作者:A. A. Krolevets、V. V. Antipova、P. V. Petrovskii、I. V. Martynov
    DOI:10.1007/bf00863934
    日期:1992.1
    The reactions of alkoxydimethylsilyl cyanides with some tetracoordinated phosphorus chlorides and fluorides were investigated. It was shown that the investigated reactions are realized primarily with the replacement of two halogen atoms by functional groups. The transformations of the phosphorus acid cyanides obtained with metal fluorides were studied.
  • Krolevets, A. A.; Martynov, I. V., Journal of general chemistry of the USSR, 1991, vol. 61, p. 236 - 236
    作者:Krolevets, A. A.、Martynov, I. V.
    DOI:——
    日期:——
  • KROLEVETS, A. A.;MARTYNOV, I. V., ZH. OBSHCH. XIMII, 61,(1991) N, S. 259
    作者:KROLEVETS, A. A.、MARTYNOV, I. V.
    DOI:——
    日期:——
  • KROLEVETS, A. A.;ANTIPOVA, V. V.;MARTYNOV, P. V., IZV. AN CCCP. CEP. XIM.,(1991) N, S. 1593-1597
    作者:KROLEVETS, A. A.、ANTIPOVA, V. V.、MARTYNOV, P. V.
    DOI:——
    日期:——
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同类化合物

(2-溴乙氧基)-特丁基二甲基硅烷 鲸蜡基聚二甲基硅氧烷 骨化醇杂质DCP 马沙骨化醇中间体 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 镓,二(1,1-二甲基乙基)甲基- 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 酰氧基丙基双封头 达格列净杂质 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Cyanomethyl[3-(trimethoxysilyl)propyl]trithiocarbonate 试剂3-[Tris(trimethylsiloxy)silyl]propylvinylcarbamate 试剂3-(Trimethoxysilyl)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]- 苯并磷杂硅杂英,5,10-二氢-10,10-二甲基-5-苯基- 苯基二甲基氯硅烷 苯基二甲基乙氧基硅 苯基二甲基(2'-甲氧基乙氧基)硅烷 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