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phenyl(2,3,4-trifluorophenyl)methanone | 243448-18-2

中文名称
——
中文别名
——
英文名称
phenyl(2,3,4-trifluorophenyl)methanone
英文别名
2,3,4-Trifluorobenzophenone;phenyl-(2,3,4-trifluorophenyl)methanone
phenyl(2,3,4-trifluorophenyl)methanone化学式
CAS
243448-18-2
化学式
C13H7F3O
mdl
MFCD00083550
分子量
236.193
InChiKey
CJDHKEHGKOZDPB-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):
    3.6
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 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:
    4

反应信息

  • 作为产物:
    描述:
    1,2,3-trifluoro-4-(1-phenylvinyl)benzene偶氮二异丁腈氧气 作用下, 以 硝基甲烷 为溶剂, 反应 12.0h, 以55%的产率得到phenyl(2,3,4-trifluorophenyl)methanone
    参考文献:
    名称:
    AIBN-Catalyzed Oxidative Cleavage of gem-Disubstituted Alkenes with O2 as an Oxidant
    摘要:
    A 2,2-azobis(isobutyronitrile) (AIBN) catalyzed oxidative cleavage of gem-disubstituted alkenes with molecular oxygen as the oxidant has been described. Carbonyl compounds were obtained as the desired products in high yield under mild conditions. Based on previous documents and current experimental results, a relatively reasonable mechanism is proposed.
    DOI:
    10.1021/jo501203a
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文献信息

  • Melt-stable poly(arylene thiotherketone) and production process thereof
    申请人:KUREHA KAGAKU KOGYO KABUSHIKI KAISHA
    公开号:EP0293115B1
    公开(公告)日:1997-09-17
  • PHOTOCHROMIC NAPHTHOPYRAN COMPOUNDS
    申请人:PPG INDUSTRIES, INC.
    公开号:EP0755527A1
    公开(公告)日:1997-01-29
  • EP0755527A4
    申请人:——
    公开号:EP0755527A4
    公开(公告)日:1997-06-18
  • ACTIVITY BASED PROBES
    申请人:University of Dundee
    公开号:EP4021926A1
    公开(公告)日:2022-07-06
  • CONTROLLED SHRINKAGE ULTRAVIOLET LIGHT RESISTANT MOLDING COMPOUND
    申请人:Guha Probir K.
    公开号:US20070197694A1
    公开(公告)日:2007-08-23
    A molding composition formulation is provided that includes a thermoset cross-linkable polymeric resin and an ultraviolet light absorber. A shrinkage-reducing polymeric additive is present in the formulation from between 3 and 30 total weight percent, such that upon cure a linear shrinkage rate of within ±1.0% is obtained. Shrinkage-reducing polymeric additives include a condensation polyester of glycol and a polyacid or acid anhydride, polyvinyl acetate, polymethylmethacrylate, or polyether polyol. A vehicle body component formed through a sheet molding composition formulation is provided as recited above, and includes a fiberglass filler. A process for producing a vehicle body component exposed to ultraviolet light upon environmental exposure of a vehicle includes molding at an elevated temperature above 20° C. the vehicle component from the formulation as detailed above. The process is followed by trimming the molded vehicle component prior to assembly.
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