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Dimethyl (2R,2'R,4S,4'S)-2,2'-dimethyl-4,4'-diphenyl-2,2'-azopentanoate | 132539-80-1

中文名称
——
中文别名
——
英文名称
Dimethyl (2R,2'R,4S,4'S)-2,2'-dimethyl-4,4'-diphenyl-2,2'-azopentanoate
英文别名
methyl (2R,4S)-2-[[(2R,4S)-1-methoxy-2-methyl-1-oxo-4-phenylpentan-2-yl]diazenyl]-2-methyl-4-phenylpentanoate
Dimethyl (2R,2'R,4S,4'S)-2,2'-dimethyl-4,4'-diphenyl-2,2'-azopentanoate化学式
CAS
132539-80-1;132618-43-0;132618-44-1;132618-45-2;132618-46-3;132618-47-4
化学式
C26H34N2O4
mdl
——
分子量
438.567
InChiKey
MBVLSAFWHHWDBV-JZKJUIAGSA-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):
    5.69
  • 重原子数:
    32.0
  • 可旋转键数:
    10.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    77.32
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

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

  • 作为产物:
    参考文献:
    名称:
    Synthesis of precursors to model styrene/methyl methacrylate copolymer radicals. .alpha.,.alpha.'-Bis(methoxycarbonyl)azoalkanes
    摘要:
    Several symmetrical alpha,alpha'-bis(methoxycarbonyl)azoalkanes 4 were prepared in high yield in two steps from the appropriate alpha-amino esters 13, or in five steps from 4-substituted 4-phenyl-2-butanones 10. The sequence involves the generation, separation, and purification of symmetrical N,N'-disubstituted sulfamides 14 followed by oxidative rearrangement under modified Ohme-Schmitz-Preuschhof conditions to yield the title compounds. In the absence of the oxidant, the sulfamides are converted quantitatively into 2,4-disubstituted 3-oxo-1,2,5-thiadiazolidine 1,1-dioxides 15. In accord with the above methodology, (4S)-4-phenyl-2-pentanone was transformed into (2R,2'R,4S,4'S)-2,2'-bis(methoxycarbonyl)-4,4'-diphenyl-2,2'-azopentane (4b-Ia), the stereochemistry of which was established from that of its precursor (2R,2'R,4S,4'S)-N,N'-bis[2-[2-(methoxycarbonyl)-4-phenylpentyl]]-sulfamide by single-crystal X-ray analysis.
    DOI:
    10.1021/jo00006a014
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