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N-(l4-boraneyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine | 186796-04-3

中文名称
——
中文别名
——
英文名称
N-(l4-boraneyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine
英文别名
——
N-(l4-boraneyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine化学式
CAS
186796-04-3
化学式
C6H22BNSi2
mdl
——
分子量
175.229
InChiKey
DUVRFEWKWIIWJI-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Reaction of Hexamethyldisilazane with Borane in Tetrahydrofuran
    摘要:
    AbstractHexamethyldisilazane 1 reacts with borane in tetrahydrofuran (THFBH3, 2) first by formation of an adduct (Me3Si)2NHBH3 (3), and then either to the N,N‐bis‐(trimethylsilyl)‐μ‐aminodiborane 5 or to the mixture of 5 and N‐trimethylsilyl‐μ‐aminodiborane(6) 6, depending on the reaction conditions. The compounds 5 and 6 can be quantitatively converted to the N,N′,N″‐tris(trimethylsilyl)borazine 4. Three intermediates can be identified, namely N,N‐bis(trimethylsilyl)borane 7, N,N‐bis(trimethylsilyl)amino(N′‐trimethylsilylamino)borane 8 and N‐trimethylsilylaminoborane‐trimer. All products and intermediates were characterized by multinuclear NMR spectroscopy, and coupling constant 1J(29Si, 15N) were measured from 29Si NMR spectra by using the Hahn‐echo‐extended (HEED) INEPT pulse sequence.
    DOI:
    10.1002/zaac.19966221208
  • 作为产物:
    参考文献:
    名称:
    Reaction of Hexamethyldisilazane with Borane in Tetrahydrofuran
    摘要:
    AbstractHexamethyldisilazane 1 reacts with borane in tetrahydrofuran (THFBH3, 2) first by formation of an adduct (Me3Si)2NHBH3 (3), and then either to the N,N‐bis‐(trimethylsilyl)‐μ‐aminodiborane 5 or to the mixture of 5 and N‐trimethylsilyl‐μ‐aminodiborane(6) 6, depending on the reaction conditions. The compounds 5 and 6 can be quantitatively converted to the N,N′,N″‐tris(trimethylsilyl)borazine 4. Three intermediates can be identified, namely N,N‐bis(trimethylsilyl)borane 7, N,N‐bis(trimethylsilyl)amino(N′‐trimethylsilylamino)borane 8 and N‐trimethylsilylaminoborane‐trimer. All products and intermediates were characterized by multinuclear NMR spectroscopy, and coupling constant 1J(29Si, 15N) were measured from 29Si NMR spectra by using the Hahn‐echo‐extended (HEED) INEPT pulse sequence.
    DOI:
    10.1002/zaac.19966221208
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