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| 1208609-55-5

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1208609-55-5
化学式
C19H17NO4
mdl
——
分子量
323.348
InChiKey
ASNZTGARMBIYSK-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

物化性质

  • 沸点:
    499.8±45.0 °C(predicted)
  • 密度:
    1.262±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

反应信息

  • 作为反应物:
    描述:
    甲醇 、 sodium hydroxide 作用下, 生成 7-hydroxy-4-((methyl(phenyl)amino)methyl)-2H-chromen-2-one
    参考文献:
    名称:
    Coumarins as novel 17β-hydroxysteroid dehydrogenase type 3 inhibitors for potential treatment of prostate cancer
    摘要:
    The synthesis and SAR studies of 3- and 4-substituted 7-hydroxycoumarins as novel 17 beta-HSD3 inhibitors are discussed. The most potent compounds from this series exhibited low nanomolar inhibitory activity with acceptable selectivity versus other 17 beta-HSD isoenzymes and nuclear receptors. (c) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.10.111
  • 作为产物:
    描述:
    Acetic acid 4-chloromethyl-2-oxo-2H-chromen-7-yl ester 、 N-甲基苯胺N,N-二甲基甲酰胺 为溶剂, 生成
    参考文献:
    名称:
    Coumarins as novel 17β-hydroxysteroid dehydrogenase type 3 inhibitors for potential treatment of prostate cancer
    摘要:
    The synthesis and SAR studies of 3- and 4-substituted 7-hydroxycoumarins as novel 17 beta-HSD3 inhibitors are discussed. The most potent compounds from this series exhibited low nanomolar inhibitory activity with acceptable selectivity versus other 17 beta-HSD isoenzymes and nuclear receptors. (c) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.10.111
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