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4-Benzyloxy-3-fluoro-2-mercapto-phenol | 620626-91-7

中文名称
——
中文别名
——
英文名称
4-Benzyloxy-3-fluoro-2-mercapto-phenol
英文别名
3-Fluoro-4-phenylmethoxy-2-sulfanylphenol
4-Benzyloxy-3-fluoro-2-mercapto-phenol化学式
CAS
620626-91-7
化学式
C13H11FO2S
mdl
——
分子量
250.294
InChiKey
JCSJLPHYQLLWJA-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):
    3.3
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    30.5
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-Benzyloxy-3-fluoro-2-mercapto-phenol三乙基硅烷三乙胺三氟乙酸 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 4-[(2S,3R)-6-Benzyloxy-5-fluoro-3-(4-triisopropylsilanyloxy-phenyl)-2,3-dihydro-benzo[1,4]oxathiin-2-yl]-phenol
    参考文献:
    名称:
    Estrogen receptor ligands. Part 4: The SAR of the syn-dihydrobenzoxathiin SERAMs
    摘要:
    A series of estrogen receptor ligands based on a dihydrobenzoxathiin scaffold is described and evaluated for estrogen/anti-estrogen activity in both in vitro and in vivo models. The most active analogue, 22, was found to be 40-fold ERalpha selective in a competitive binding assay, and 22 demonstrated very potent in vivo antagonism of estradiol driven proliferation in an immature rat uterine weight gain assay. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.03.074
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文献信息

  • Estrogen receptor ligands. Part 4: The SAR of the syn-dihydrobenzoxathiin SERAMs
    作者:Seongkon Kim、Jane Wu、Helen Y. Chen、Elizabeth T. Birzin、Wanda Chan、Yi Tien Yang、Lawrence Colwell、Susan Li、Johanna Dahllund、Frank DiNinno、Susan P. Rohrer、James M. Schaeffer、Milton L. Hammond
    DOI:10.1016/j.bmcl.2004.03.074
    日期:2004.6
    A series of estrogen receptor ligands based on a dihydrobenzoxathiin scaffold is described and evaluated for estrogen/anti-estrogen activity in both in vitro and in vivo models. The most active analogue, 22, was found to be 40-fold ERalpha selective in a competitive binding assay, and 22 demonstrated very potent in vivo antagonism of estradiol driven proliferation in an immature rat uterine weight gain assay. (C) 2004 Elsevier Ltd. All rights reserved.
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