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[1-11C]phenol

中文名称
——
中文别名
——
英文名称
[1-11C]phenol
英文别名
(111C)cyclohexatrienol
[1-11C]phenol化学式
CAS
——
化学式
C6H6O
mdl
——
分子量
93.102
InChiKey
ISWSIDIOOBJBQZ-KWCOIAHCSA-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):
    1.5
  • 重原子数:
    7
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    [1-11C]aniline氢溴酸 、 sodium nitrite 作用下, 以 为溶剂, 反应 0.08h, 生成 [1-11C]phenol
    参考文献:
    名称:
    Synthesis of [1-11C]phenol
    摘要:
    The synthesis of no-carrier-added [1-C-11]phenol (3) which is a further important aromatic C-11 unit for potential PET radiotracers is described for the first time. [1-C-11]Aniline (1) was diazotized and the [1-C-11]benzenediazonium bromide (2) formed was concentrated in situ to give 3. Before diazotization, 1 had to be purified twice by means of an adsorber resin and a cation exchange resin. Starting from the purified 1, 3 was obtained in a radiochemical purity of about 79 % within 10 min. Related to crude 1 from the one-pot process, the reproducible radiochemical yield of 3 was about 16 % (decay-corrected). C-13/C-11 Go-labelling experiments were carried out in order to confirm the identity of 3 and the position of the label.
    DOI:
    10.1002/(sici)1099-1344(200005)43:6<557::aid-jlcr341>3.0.co;2-u
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文献信息

  • Synthesis of [1-11C]phenol
    作者:P. M�ding、J. Steinbach
    DOI:10.1002/(sici)1099-1344(200005)43:6<557::aid-jlcr341>3.0.co;2-u
    日期:2000.5
    The synthesis of no-carrier-added [1-C-11]phenol (3) which is a further important aromatic C-11 unit for potential PET radiotracers is described for the first time. [1-C-11]Aniline (1) was diazotized and the [1-C-11]benzenediazonium bromide (2) formed was concentrated in situ to give 3. Before diazotization, 1 had to be purified twice by means of an adsorber resin and a cation exchange resin. Starting from the purified 1, 3 was obtained in a radiochemical purity of about 79 % within 10 min. Related to crude 1 from the one-pot process, the reproducible radiochemical yield of 3 was about 16 % (decay-corrected). C-13/C-11 Go-labelling experiments were carried out in order to confirm the identity of 3 and the position of the label.
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