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4-Chloro-3,3,4,4-tetrafluorobutanal | 131118-28-0

中文名称
——
中文别名
——
英文名称
4-Chloro-3,3,4,4-tetrafluorobutanal
英文别名
——
4-Chloro-3,3,4,4-tetrafluorobutanal化学式
CAS
131118-28-0
化学式
C4H3ClF4O
mdl
——
分子量
178.514
InChiKey
WXCUSEKTKJXMRQ-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):
    1.7
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    4-硝基苯胺4-Chloro-3,3,4,4-tetrafluorobutanal乙腈 为溶剂, 反应 2.0h, 以83%的产率得到(Z)-4-[(4-nitrophenyl)amino]-1,1-difluoro-1-chloro-3-buten-2-one
    参考文献:
    名称:
    Reactions of 2,2-dihydropolyfluoroalkylaldehydes with amines: a facile synthetic method for fluoroalkyl enaminoketones
    摘要:
    Reactions of 2,2-dihydropolyfluoroalkylaldehydes (1) with amines (2) were studied. Both aliphatic amines and electron-deficient aromatic amines readily reacted with I in acetonitrile and water under reflux to give fluoroalkyl enaminoketones (3) in high yields, while no condensed products were obtained by reactions of 1 with electron-rich aromatic amines under similar conditions. In the presence of triethylamine, however, the reaction of 1 with electron-rich aromatic amines at room temperature gave 3 in low yields. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2003.11.005
  • 作为产物:
    描述:
    1-氯-2-碘四氟乙烷,乙烯基乙醚 在 sodium dithionite 作用下, 以 乙腈 为溶剂, 生成 4-Chloro-3,3,4,4-tetrafluorobutanal
    参考文献:
    名称:
    Synthesis of 5-per(poly)fluoroalkyl-2,3-dihydro-1,4-diazepines
    摘要:
    a series of 5-per(poly)fluoroalkyl-2,3-dihydro-1,4-diazepines were synthesized from alpha-per(poly)fluoroalkyl aldehydes and ethylenediamine. A possible reaction pathway was suggested. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(98)00261-5
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文献信息

  • A Novel Synthesis of 2-Fluoroalkyl Quinolines
    作者:Quan-Fu Wang、Yun-Yu Mao、Chao-Yue Qin、Shi-Zheng Zhu、Chang-Ming Hu
    DOI:10.1007/s007060050006
    日期:2000.1.15
    2-Fluoroalkyl quinolines are prepared by reacting aniline with alpha-fluoroalkyl aldehydes or alpha-fluoroalkyl cyclohexanones in the presence of acetic acid. Under the same reaction condition, 2-aminophenol gives the corresponding 2-fluoroalkyl-8-quinolinols; in some cases, 2-fluoroalkyl benzoxazoles are also formed as minor products.
  • A novel synthesis of 2-per(poly)fluoroalkyl-1H-benzimidazoles or 2-per(poly) fluoroalkyl benzothiazoles
    作者:Quan-Fu Wang、Yun-Yu Mao、Shi-Zheng Zhu、Chang-Ming Hu
    DOI:10.1016/s0022-1139(99)00012-3
    日期:1999.6
    A new method for the preparation of 2-per(poly)fluoroalkyl-1H-benzimidazoles or 2-per(poly)fluoroalkyl benzothiazoles from reaction of readily available alpha-per(poly)fluoroalkyl aldehydes with o-phenylenediamine or 2-aminobenzenethiol is presented. A possible reaction pathway is suggested. (C) 1999 Elsevier Science S.A. All rights reserved.
  • Synthesis of 5-per(poly)fluoroalkyl-2,3-dihydro-1,4-diazepines
    作者:Quan-Fu Wang、Bin Hu、Bing-Hao Luo、Chang-Ming Hu
    DOI:10.1016/s0040-4039(98)00261-5
    日期:1998.4
    a series of 5-per(poly)fluoroalkyl-2,3-dihydro-1,4-diazepines were synthesized from alpha-per(poly)fluoroalkyl aldehydes and ethylenediamine. A possible reaction pathway was suggested. (C) 1998 Elsevier Science Ltd. All rights reserved.
  • Reactions of 2,2-dihydropolyfluoroalkylaldehydes with amines: a facile synthetic method for fluoroalkyl enaminoketones
    作者:Xian-Jin Yang、Jin-Tao Liu、Fu-Lu Zhao
    DOI:10.1016/j.jfluchem.2003.11.005
    日期:2004.3
    Reactions of 2,2-dihydropolyfluoroalkylaldehydes (1) with amines (2) were studied. Both aliphatic amines and electron-deficient aromatic amines readily reacted with I in acetonitrile and water under reflux to give fluoroalkyl enaminoketones (3) in high yields, while no condensed products were obtained by reactions of 1 with electron-rich aromatic amines under similar conditions. In the presence of triethylamine, however, the reaction of 1 with electron-rich aromatic amines at room temperature gave 3 in low yields. (C) 2003 Elsevier B.V. All rights reserved.
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