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3-chloro-3-(4-methylphenoxy)diazirine | 307514-61-0

中文名称
——
中文别名
——
英文名称
3-chloro-3-(4-methylphenoxy)diazirine
英文别名
3-Chloro-3-(4-methylphenoxy)-3H-diazirene
3-chloro-3-(4-methylphenoxy)diazirine化学式
CAS
307514-61-0
化学式
C8H7ClN2O
mdl
——
分子量
182.609
InChiKey
ZPPJRYHPJGDUEL-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):
    3
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    34
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    丁炔二酸二乙酯3-chloro-3-(4-methylphenoxy)diazirine甲苯 为溶剂, 反应 15.0h, 以34%的产率得到1,4-bis(4-methylphenoxy)-1,4-dichloro-2,3-diazabuta-1,3-diene
    参考文献:
    名称:
    Interaction of Aryloxychlorocarbenes with Acetylenedicarboxylate:  Novel Formation of Polyfunctional Butadienes and 8-Oxatricyclo[3.2.1.02.4]oct-6-enes
    摘要:
    The interaction of aryloxychlorocarbenes with dialkyl acetylenedicarboxylates has been examined. Thermolyses of 3-aryloxy-3-chlorodiazirines in the presence of acetylenedicarboxylate resulted in the formation of unexpected polyfunctional 1,3-butadienes and 8-oxatricyclo[3.2.1.0(2.4)]oct-6-enes or of 2-aryoxycarbonylmaleates dependent upon reaction conditions. This work confirmed the nucleophilicity of aryloxychlorocarbenes and underlined their synthetic potential.
    DOI:
    10.1021/jo0501792
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文献信息

  • Interaction of Aryloxychlorocarbenes with Acetylenedicarboxylate:  Novel Formation of Polyfunctional Butadienes and 8-Oxatricyclo[3.2.1.0<sup>2.4</sup>]oct-6-enes
    作者:Ying Cheng、Qing Zhu、Quan Song Li、Otto Meth-Cohn
    DOI:10.1021/jo0501792
    日期:2005.6.1
    The interaction of aryloxychlorocarbenes with dialkyl acetylenedicarboxylates has been examined. Thermolyses of 3-aryloxy-3-chlorodiazirines in the presence of acetylenedicarboxylate resulted in the formation of unexpected polyfunctional 1,3-butadienes and 8-oxatricyclo[3.2.1.0(2.4)]oct-6-enes or of 2-aryoxycarbonylmaleates dependent upon reaction conditions. This work confirmed the nucleophilicity of aryloxychlorocarbenes and underlined their synthetic potential.
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