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(E)-3-(4-fluorophenyl)-1-(4-methyl-2-(methylamino)thiazol-5-yl)prop-2-en-1-one | 1350802-15-1

中文名称
——
中文别名
——
英文名称
(E)-3-(4-fluorophenyl)-1-(4-methyl-2-(methylamino)thiazol-5-yl)prop-2-en-1-one
英文别名
(E)-3-(4-fluorophenyl)-1-[4-methyl-2-(methylamino)-1,3-thiazol-5-yl]prop-2-en-1-one
(E)-3-(4-fluorophenyl)-1-(4-methyl-2-(methylamino)thiazol-5-yl)prop-2-en-1-one化学式
CAS
1350802-15-1
化学式
C14H13FN2OS
mdl
——
分子量
276.334
InChiKey
XQOQSIRCTSOXLE-VMPITWQZSA-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):
    3.9
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    70.2
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    3-氯-2,4-戊二酮 在 sodium hydroxide 作用下, 以 甲醇丙酮 为溶剂, 反应 1.5h, 生成 (E)-3-(4-fluorophenyl)-1-(4-methyl-2-(methylamino)thiazol-5-yl)prop-2-en-1-one
    参考文献:
    名称:
    Novel (E)-1-(4-methyl-2-(alkylamino)thiazol-5-yl)-3-arylprop-2-en-1-ones as potent antimicrobial agents
    摘要:
    New (E)-1-(4-methyl-2-(alkylamino)thiazol-5-yl)-3-arylprop-2-en-1-ones, unsubstituted or carrying fluoro, bromo, methoxy, nitro, methyl and chloro groups on the benzene ring, were synthesized and assayed in vitro for their antimicrobial activity against Gram positive and Gram negative bacteria and fungi. The compounds were very potent towards all tested microorganisms and in most cases their activity was better than that of reference drugs. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2011.10.059
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文献信息

  • Novel (E)-1-(4-methyl-2-(alkylamino)thiazol-5-yl)-3-arylprop-2-en-1-ones as potent antimicrobial agents
    作者:K. Liaras、A. Geronikaki、J. Glamočlija、A. Ćirić、M. Soković
    DOI:10.1016/j.bmc.2011.10.059
    日期:2011.12
    New (E)-1-(4-methyl-2-(alkylamino)thiazol-5-yl)-3-arylprop-2-en-1-ones, unsubstituted or carrying fluoro, bromo, methoxy, nitro, methyl and chloro groups on the benzene ring, were synthesized and assayed in vitro for their antimicrobial activity against Gram positive and Gram negative bacteria and fungi. The compounds were very potent towards all tested microorganisms and in most cases their activity was better than that of reference drugs. (C) 2011 Elsevier Ltd. All rights reserved.
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