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di-tert-butyldiazidosilane | 116077-31-7

中文名称
——
中文别名
——
英文名称
di-tert-butyldiazidosilane
英文别名
Diazido(ditert-butyl)silane
di-tert-butyldiazidosilane化学式
CAS
116077-31-7
化学式
C8H18N6Si
mdl
——
分子量
226.357
InChiKey
YEXHDDGEKUVERC-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):
    4.65
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    28.7
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    di-tert-butyldiazidosilane正戊烷 为溶剂, 生成 4,8-bis(bis(trimethylsilyl)methyl)-6,6-di-tert-butyl-2,2,10,10-tetramethyl-3,9-bis(trimethylsilyl)-5,7-diaza-2,6,10-trisila-4,8-digermaundecane-4,8-diol
    参考文献:
    名称:
    双(锗烷亚胺)的合成,结构和光反应
    摘要:
    The reaction of bis[bis(trimethylsilyl)methyl]-germylene (1) with N-(azidosilyl)germanimines 3a,b at room temperature gave bis(germanimines) 4a,b in quantitative yield whose structures have been confirmed by single-crystal X-ray diffraction. The photolysis of 4a gave the cyclic silanimine 6 as an unexpected product.
    DOI:
    10.1021/om00014a013
  • 作为产物:
    描述:
    二叔丁基氯硅烷 在 sodium azide 作用下, 以 乙腈 为溶剂, 反应 3.0h, 以93%的产率得到di-tert-butyldiazidosilane
    参考文献:
    名称:
    The photochemistry of matrix-isolated di-tert-butyldiazidosilane. Observation of di-tert-butylsilylene and N,N'-di-tert-butylsilanediimine
    摘要:
    DOI:
    10.1021/ja00228a014
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文献信息

  • WELSH, KEVIN M.;MICHI, JOSEF;WEST, ROBERT, J. AMER. CHEM. SOC., 110,(1988) N 20, C. 6689-6696
    作者:WELSH, KEVIN M.、MICHI, JOSEF、WEST, ROBERT
    DOI:——
    日期:——
  • The photochemistry of matrix-isolated di-tert-butyldiazidosilane. Observation of di-tert-butylsilylene and N,N'-di-tert-butylsilanediimine
    作者:Kevin M. Welsh、Josef. Michl、Robert. West
    DOI:10.1021/ja00228a014
    日期:1988.9
  • Synthesis, Structure, and Photoreaction of Bis(germanimines)
    作者:Wataru Ando、Toshiyuki Ohtaki、Yoshio Kabe
    DOI:10.1021/om00014a013
    日期:1994.2
    The reaction of bis[bis(trimethylsilyl)methyl]-germylene (1) with N-(azidosilyl)germanimines 3a,b at room temperature gave bis(germanimines) 4a,b in quantitative yield whose structures have been confirmed by single-crystal X-ray diffraction. The photolysis of 4a gave the cyclic silanimine 6 as an unexpected product.
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同类化合物

叠氮(二丁基)硼烷 二乙酰氧基二甲基硅烷 三甲基甲硅烷基锡 三正丁基叠氮化锡 N,N,N',N'-四甲基胍叠氮化物 BROMO-PEG1-AZIDE,BROMO-PEG1-N3,溴代-聚乙二醇-叠氮 1,3-二叠氮基-1,1,3,3-四丁基二锡氧烷 (c-C6H11)2BN3 Me2AlN3 [triethyl][azido]tin 3-(4-azidophenyl)propiolonitrile diazido[tris(trimethylsilyl)methyl]borane azotriethyleneoxydodecane disulfide Azido-bromo-di-tert-butylsilan Azido-di-tert-butyl-fluorsilan Dibutylphosphoryl-azid 1,1-Dicyano-2,2-diazidoethylene Azido-di(propan-2-yl)borane Azido-bis(2-methylpropyl)borane bis-(azido-di-n-propyl-tin)-oxide Trimethyl-germanylazid O-Aethyl-methylphosphonazidothioat tBuSi(N3)3 1-azido-2,2,3,4,4-pentamethyl-phosphetane 1-oxide Dimethylthionophosphinsaeureazid diazidomethane Diazidopropanedinitrile N-azido-N-methoxyformamide Tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)stannanylium;azide 1,3,5,7-tetra(tert-butyl)-2,4,6,8-tetraazido-borazocine diszidomethylsilane 2-Azido-1,3-dimethyl-1,3,2-diazaborolidin tris(cyclohexyl)tin azide 2,2-diazido-3-methyl-butane N-[azido-bromo-bis(dimethylamino)-lambda5-phosphanyl]-N-methylmethanamine Azidodi-tert-butylsilan azidodichlorobis(2,2,2-trichloro-1,1-dimethylethyl)phosphorane triethylammonium azide azidodimethylborane dipropyl-boron azide di-isopropylphosphinic azide diazido-tert-butylborane azido isocyanate dimethylzinndiazid Diethylgallium azide dimethylgallium azide 2,2,3-Triazido-1-(3,3,4-triazidobutan-2-yloxy)butane Bis(azidosulfanyl)methane