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1,1'-羰基二咪唑-13C | 181517-09-9

中文名称
1,1'-羰基二咪唑-13C
中文别名
——
英文名称
1,1-carbonyl diimidazole-[13C]
英文别名
1,1'-Carbonyldiimidazole-13C;di(imidazol-1-yl)(113C)methanone
1,1'-羰基二咪唑-13C化学式
CAS
181517-09-9
化学式
C7H6N4O
mdl
——
分子量
163.14
InChiKey
PFKFTWBEEFSNDU-CDYZYAPPSA-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):
    -0.2
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    52.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1,1'-羰基二咪唑-13C 、 4,5,6-triaminopyrimidine-[2-13C-15N3] 以 N,N-二甲基甲酰胺 为溶剂, 反应 12.0h, 生成 8-hydroxyadenine-[1,3,7-15N3-2,8-13C2]
    参考文献:
    名称:
    Synthesis of isotopically labelled DNA degradation products for use in mass spectrometric studies of cellular DNA damage
    摘要:
    Thirteen substituted purines and pyrimidines bearing from three to five carbon, nitrogen and/or deuterium isotopic labels have been synthesized in yields ranging from .1 to 70%. Most of the products originate from the same small number of commercially available labelled starting materials, and in several cases one intermediate leads to two products, thus minimizing the expense and time required. The parent compounds are found in tissue as the result of DNA damage often linked with carcinogenesis and mutagenesis. The synthesized compounds serve as internal standards for the study of DNA damage using mass spectrometry.
    DOI:
    10.1002/(sici)1099-1344(199608)38:8<713::aid-jlcr886>3.0.co;2-i
  • 作为产物:
    描述:
    咪唑光气-13C 为溶剂, 生成 1,1'-羰基二咪唑-13C
    参考文献:
    名称:
    Synthesis of isotopically labelled DNA degradation products for use in mass spectrometric studies of cellular DNA damage
    摘要:
    Thirteen substituted purines and pyrimidines bearing from three to five carbon, nitrogen and/or deuterium isotopic labels have been synthesized in yields ranging from .1 to 70%. Most of the products originate from the same small number of commercially available labelled starting materials, and in several cases one intermediate leads to two products, thus minimizing the expense and time required. The parent compounds are found in tissue as the result of DNA damage often linked with carcinogenesis and mutagenesis. The synthesized compounds serve as internal standards for the study of DNA damage using mass spectrometry.
    DOI:
    10.1002/(sici)1099-1344(199608)38:8<713::aid-jlcr886>3.0.co;2-i
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文献信息

  • Synthesis of isotopically labelled DNA degradation products for use in mass spectrometric studies of cellular DNA damage
    作者:Victor C. Nelson
    DOI:10.1002/(sici)1099-1344(199608)38:8<713::aid-jlcr886>3.0.co;2-i
    日期:1996.8
    Thirteen substituted purines and pyrimidines bearing from three to five carbon, nitrogen and/or deuterium isotopic labels have been synthesized in yields ranging from .1 to 70%. Most of the products originate from the same small number of commercially available labelled starting materials, and in several cases one intermediate leads to two products, thus minimizing the expense and time required. The parent compounds are found in tissue as the result of DNA damage often linked with carcinogenesis and mutagenesis. The synthesized compounds serve as internal standards for the study of DNA damage using mass spectrometry.
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