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5-(4-(2-(fluoro-18F)ethoxy)phenyl)-2-phenyl-2H-tetrazole | 1319719-73-7

中文名称
——
中文别名
——
英文名称
5-(4-(2-(fluoro-18F)ethoxy)phenyl)-2-phenyl-2H-tetrazole
英文别名
——
5-(4-(2-(fluoro-18F)ethoxy)phenyl)-2-phenyl-2H-tetrazole化学式
CAS
1319719-73-7
化学式
C15H13FN4O
mdl
——
分子量
283.294
InChiKey
FQTTVMZVGOYHCE-GKTGUEEDSA-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):
    2.68
  • 重原子数:
    21.0
  • 可旋转键数:
    5.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    52.83
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

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

  • 作为反应物:
    描述:
    5-(4-(2-(fluoro-18F)ethoxy)phenyl)-2-phenyl-2H-tetrazole乙腈 为溶剂, 反应 0.08h, 生成
    参考文献:
    名称:
    Photoactivated 1,3-dipolar cycloaddition for the rapid preparation of 18F labelled radiotracers
    摘要:
    An F-18-labelled 2,5-diaryl tetrazole reagent has been prepared and reacted with substituted alkene dipolarophiles through a photoactivated 1,3-dipolar cycloaddition reaction. The radiobioconjugation reaction furnished the desired product in 5 min with radiochemical conversions of 85-95% at room temperature. Remarkably, for the activated dipolarophiles, these results were obtained in highly dilute solutions (10-100 mu M). (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.05.122
  • 作为产物:
    描述:
    参考文献:
    名称:
    Photoactivated 1,3-dipolar cycloaddition for the rapid preparation of 18F labelled radiotracers
    摘要:
    An F-18-labelled 2,5-diaryl tetrazole reagent has been prepared and reacted with substituted alkene dipolarophiles through a photoactivated 1,3-dipolar cycloaddition reaction. The radiobioconjugation reaction furnished the desired product in 5 min with radiochemical conversions of 85-95% at room temperature. Remarkably, for the activated dipolarophiles, these results were obtained in highly dilute solutions (10-100 mu M). (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.05.122
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