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Tert-butyl 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]ethyl carbonate | 305857-41-4

中文名称
——
中文别名
——
英文名称
Tert-butyl 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]ethyl carbonate
英文别名
——
Tert-butyl 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]ethyl carbonate化学式
CAS
305857-41-4
化学式
C13H25NO5
mdl
——
分子量
275.345
InChiKey
VCDYNBBQFZHIIJ-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):
    2.4
  • 重原子数:
    19
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.85
  • 拓扑面积:
    65.1
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Di-<i>tert</i>-butyl Dicarbonate and 4-(Dimethylamino)pyridine Revisited. Their Reactions with Amines and Alcohols<sup>1</sup>
    作者:Yochai Basel、Alfred Hassner
    DOI:10.1021/jo000257f
    日期:2000.10.1
    The reaction of BOC2O in the presence and absence of DMAP was examined with some amines, alcohols, diols, amino alcohols, and aminothiols. Often, unusual products were observed depending on the ratio of reagents, reaction time, polarity of solvent, pK(a) of alcohols, or type of amine (primary or secondary). In reactions of aliphatic alcohols with BOC2O/DMAP, we isolated for the first time carbonic-carbonic anhydride intermediates; this helps explain the formation of symmetrical carbonates in addition to the O-BOC products. In the case of secondary amines, we succeeded to isolate unstable carbamic-carbonic anhydride intermediates that in the presence of DMAP led to the final N-BOC product. The effect of N-methylimidazole in place of DMAP was also examined.
  • DRUG COMPOSITION HAVING ACTIVE INGREDIENT ADHERED AT HIGH CONCENTRATION TO SPHERICAL CORE
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP1602362B1
    公开(公告)日:2016-09-28
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