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3-nitroso-3-methylbutanoic acid methyl ester | 49680-44-6

中文名称
——
中文别名
——
英文名称
3-nitroso-3-methylbutanoic acid methyl ester
英文别名
methyl β-nitrosoisovalerate;Methyl-3-methyl-3-nitrosobutanoat;Methyl 3-methyl-3-nitrosobutanoate
3-nitroso-3-methylbutanoic acid methyl ester化学式
CAS
49680-44-6
化学式
C6H11NO3
mdl
——
分子量
145.158
InChiKey
LQQRIFSFLSDMIW-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:
    174.1±23.0 °C(Predicted)
  • 密度:
    1.05±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    55.7
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    3-nitroso-3-methylbutanoic acid methyl ester 、 dimethoxyaminyl radical 以 乙醚 为溶剂, 反应 0.5h, 以56%的产率得到N(1,1-dimethyl-2-methoxycarbonyl)ethyl-N'-methoxydiazene N-oxide
    参考文献:
    名称:
    Reaction of the dimethoxyaminyl radical with tertiary nitrosoalkanes as a method for the preparation of N-alkyl-N?-methoxydiazene N-oxides
    摘要:
    The reaction of the dimethoxyaminyl radical with functionally substituted nitrosoalkanes (2) in a 2:1 ratio at 20-degrees-C gives the corresponding N-alkyl-N'-methoxydiazene N-oxides (3) as a single isomer in preparative yields.
    DOI:
    10.1007/bf00863834
  • 作为产物:
    参考文献:
    名称:
    Peracid oxidation of imino ethers
    摘要:
    DOI:
    10.1021/jo00940a012
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文献信息

  • Reactions of N-chloro-N-alkoxy-tert-alkylamines with isobutylene and methanol
    作者:V. G. Shtamburg、V. F. Rudchenko、V. M. Grinev、A. A. Dmitrenko、A. P. Pleshkova、R. G. Kostyanovskii
    DOI:10.1007/bf00961356
    日期:1991.5
    The addition of N-chloro-N-methoxy-tert-alkylamines to an olefin, which is assumed to proceed with the participation of alkoxynitrenium ions, was carried out for the first time. The methanolysis of N-chloro-N-alkoxy-tert-alkylamines in the presence of Et3N gives dialkoxyamines, and depending on the type of the N-alkyl substituent is accompanied by side reactions.
  • SHTAMBURG, V. G.;RUDCHENKO, V. F.;GRINEV, V. M.;DMITRENKO, A. A.;PLESHKOV+, IZV. AN CCCP. CEP. XIM.,(1991) N, S. 1069-1072
    作者:SHTAMBURG, V. G.、RUDCHENKO, V. F.、GRINEV, V. M.、DMITRENKO, A. A.、PLESHKOV+
    DOI:——
    日期:——
  • Peracid oxidation of imino ethers
    作者:Donald H. Aue、Darryl Thomas
    DOI:10.1021/jo00940a012
    日期:1974.12
  • Reaction of the dimethoxyaminyl radical with tertiary nitrosoalkanes as a method for the preparation of N-alkyl-N?-methoxydiazene N-oxides
    作者:V. F. Rudchenko、S. M. Ignatov、R. G. Kostyanovskii
    DOI:10.1007/bf00863834
    日期:1992.10
    The reaction of the dimethoxyaminyl radical with functionally substituted nitrosoalkanes (2) in a 2:1 ratio at 20-degrees-C gives the corresponding N-alkyl-N'-methoxydiazene N-oxides (3) as a single isomer in preparative yields.
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