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7-[5-(4-Methoxy-phenyl)-oxazol-2-yl]-heptanoic acid | 847265-50-3

中文名称
——
中文别名
——
英文名称
7-[5-(4-Methoxy-phenyl)-oxazol-2-yl]-heptanoic acid
英文别名
7-[5-(4-methoxyphenyl)-1,3-oxazol-2-yl]heptanoic acid
7-[5-(4-Methoxy-phenyl)-oxazol-2-yl]-heptanoic acid化学式
CAS
847265-50-3
化学式
C17H21NO4
mdl
——
分子量
303.358
InChiKey
DTHZOGJYCNHQSN-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:
    487.0±35.0 °C(Predicted)
  • 密度:
    1.145±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.93
  • 重原子数:
    22.0
  • 可旋转键数:
    9.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    72.56
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    7-[5-(4-Methoxy-phenyl)-oxazol-2-yl]-heptanoic acid羟胺三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 7-[5-(4-Methoxy-phenyl)-oxazol-2-yl]-heptanoic acid hydroxyamide
    参考文献:
    名称:
    A novel series of histone deacetylase inhibitors incorporating hetero aromatic ring systems as connection units
    摘要:
    A series of structurally novel HDAC inhibitors, in which a hetero aromatic ring connects the spacer with the hydrophobic group, has been designed and synthesized. These new inhibitors are very potent in in vitro enzymatic assays and display antiproliferation activity against two human cancer cell lines. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2003.07.012
  • 作为产物:
    参考文献:
    名称:
    A novel series of histone deacetylase inhibitors incorporating hetero aromatic ring systems as connection units
    摘要:
    A series of structurally novel HDAC inhibitors, in which a hetero aromatic ring connects the spacer with the hydrophobic group, has been designed and synthesized. These new inhibitors are very potent in in vitro enzymatic assays and display antiproliferation activity against two human cancer cell lines. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2003.07.012
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