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3-(3,4-difluorophenyl)-1-phenyl-(2E)-2-propen-1-one | 1354382-13-0

中文名称
——
中文别名
——
英文名称
3-(3,4-difluorophenyl)-1-phenyl-(2E)-2-propen-1-one
英文别名
3-(3,4-difluorophenyl)-1-pnenyl-(2E)-2-propen-1-one;(E)-3-(3,4-difluorophenyl)-1-phenylprop-2-en-1-one
3-(3,4-difluorophenyl)-1-phenyl-(2E)-2-propen-1-one化学式
CAS
1354382-13-0
化学式
C15H10F2O
mdl
——
分子量
244.241
InChiKey
VNLFNIRJXBOQRP-VQHVLOKHSA-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:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    N-(4-nitrophenyl)-3-amino-3-(3,4-difluorophenyl)-1-phenylprop-1-yne 在 montmorillonite clay doped with CuCl 、 air 作用下, 反应 0.08h, 以55%的产率得到3-(3,4-difluorophenyl)-1-phenyl-(2E)-2-propen-1-one
    参考文献:
    名称:
    Microwave promoted one-pot preparation of fluorinated propargylamines and their chemical transformation
    摘要:
    A series of fluorinated propargylamines have been synthesized from the one-pot three-component reaction of fluorobenzaldehyde, aniline and phenylacetylene under solvent-free and microwave irradiation. The fluorinated propargylamines were then further transformed to chalcones or quinoline derivatives respectively depending on the different structures of propargylamines. (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2011.08.005
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文献信息

  • Microwave promoted one-pot preparation of fluorinated propargylamines and their chemical transformation
    作者:Xiao-Lei Chen、Jian-Min Zhang、Wen-Li Shang、Bei-Qiong Lu、Jian-An Jin
    DOI:10.1016/j.jfluchem.2011.08.005
    日期:2012.1
    A series of fluorinated propargylamines have been synthesized from the one-pot three-component reaction of fluorobenzaldehyde, aniline and phenylacetylene under solvent-free and microwave irradiation. The fluorinated propargylamines were then further transformed to chalcones or quinoline derivatives respectively depending on the different structures of propargylamines. (C) 2011 Elsevier B.V. All rights reserved.
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