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3-(2-chlorophenyl)-1-(furan-2-yl)-3-(phenylthio)propan-1-one | 1373122-02-1

中文名称
——
中文别名
——
英文名称
3-(2-chlorophenyl)-1-(furan-2-yl)-3-(phenylthio)propan-1-one
英文别名
3-(2-Chlorophenyl)-1-(furan-2-yl)-3-phenylsulfanylpropan-1-one
3-(2-chlorophenyl)-1-(furan-2-yl)-3-(phenylthio)propan-1-one化学式
CAS
1373122-02-1
化学式
C19H15ClO2S
mdl
——
分子量
342.846
InChiKey
KXNXATTYNVEWTB-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):
    5.3
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    55.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    3-(2-Chlorophenyl)-1-(furan-2-yl)prop-2-en-1-one苯硫酚 作用下, 以 二氯甲烷 为溶剂, 反应 3.0h, 以82%的产率得到3-(2-chlorophenyl)-1-(furan-2-yl)-3-(phenylthio)propan-1-one
    参考文献:
    名称:
    Synthesis and Screening Antimicrobial Activities of Novel 1,3-Diaryl-3- (Phenylthio)Propan-1-One Derivatives
    摘要:
    In this study, a series of novel beta-mercapto carbonyl derivatives (3a-j) was prepared by addition of thiophenol (2) to chalcones (1a-j) in the presence of catalytic amount of iodine (10 mol%) in CH2Cl2. Antibacterial and antifungal in vitro properties of the synthesized compounds were tested against some human pathogenic microorganisms by employing the disk diffusion technique. For the most active compounds, also minimum inhibitory concentrations (MICs) were determined.
    DOI:
    10.1080/10426507.2011.632387
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文献信息

  • Synthesis and Screening Antimicrobial Activities of Novel 1,3-Diaryl-3- (Phenylthio)Propan-1-One Derivatives
    作者:İsa Karaman、Hayreddin Gezegen、Mustafa Ceylan、Merve Dilmaç
    DOI:10.1080/10426507.2011.632387
    日期:2012.5
    In this study, a series of novel beta-mercapto carbonyl derivatives (3a-j) was prepared by addition of thiophenol (2) to chalcones (1a-j) in the presence of catalytic amount of iodine (10 mol%) in CH2Cl2. Antibacterial and antifungal in vitro properties of the synthesized compounds were tested against some human pathogenic microorganisms by employing the disk diffusion technique. For the most active compounds, also minimum inhibitory concentrations (MICs) were determined.
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