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4-[(2-Amino-4-phenyl-1,3-thiazol-5-yl)methyl]phenol | 946425-52-1

中文名称
——
中文别名
——
英文名称
4-[(2-Amino-4-phenyl-1,3-thiazol-5-yl)methyl]phenol
英文别名
——
4-[(2-Amino-4-phenyl-1,3-thiazol-5-yl)methyl]phenol化学式
CAS
946425-52-1
化学式
C16H14N2OS
mdl
——
分子量
282.366
InChiKey
DAJMAOFJALKMKO-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:
    536.1±38.0 °C(Predicted)
  • 密度:
    1.298±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    87.4
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-[(2-Amino-4-phenyl-1,3-thiazol-5-yl)methyl]phenol1-methyl-3-trimethylsilylparabanic acid甲苯 为溶剂, 反应 18.0h, 生成 5-[[5-[(4-Hydroxyphenyl)methyl]-4-phenyl-1,3-thiazol-2-yl]imino]-3-methylimidazolidine-2,4-dione
    参考文献:
    名称:
    Synthesis and biological evaluation of analogues of the anti-tumor alkaloid naamidine A
    摘要:
    A small series of derivatives of the alkaloid naamidine A was synthesized and tested in vitro for their ability to inhibit mitogenesis in BaF/ERX cells. Replacement of the imidazole core with a thiazole was found to have only a minor effect on potency, and the 4-metlioxybenzyl substituent of the natural product was shown to be unnecessary for activity. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.04.017
  • 作为产物:
    参考文献:
    名称:
    Synthesis and biological evaluation of analogues of the anti-tumor alkaloid naamidine A
    摘要:
    A small series of derivatives of the alkaloid naamidine A was synthesized and tested in vitro for their ability to inhibit mitogenesis in BaF/ERX cells. Replacement of the imidazole core with a thiazole was found to have only a minor effect on potency, and the 4-metlioxybenzyl substituent of the natural product was shown to be unnecessary for activity. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.04.017
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