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dichloro-fluoro-acetyl chloride | 354-17-6

中文名称
——
中文别名
——
英文名称
dichloro-fluoro-acetyl chloride
英文别名
Dichlor-fluor-acetylchlorid;Acetyl chloride, dichlorofluoro-;2,2-dichloro-2-fluoroacetyl chloride
dichloro-fluoro-acetyl chloride化学式
CAS
354-17-6
化学式
C2Cl3FO
mdl
——
分子量
165.379
InChiKey
BWAQLYSNPAWYRG-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

物化性质

  • 沸点:
    73.2±35.0 °C(Predicted)
  • 密度:
    1.682±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    7
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    dichloro-fluoro-acetyl chloride 、 在 sodium hydroxide 作用下, 生成 α,α'-Bis-(ethyl-fluordichloracetyl-amino)-p-xylol
    参考文献:
    名称:
    New Amorbacides--VI. The Preparation of some N,N'-Disubstituted-N,N'-bis(haloacyl)-1,4-xylylenediamines
    摘要:
    DOI:
    10.1021/jm50016a001
  • 作为产物:
    描述:
    三氯乙酸酐三氟化锑 作用下, 生成 dichloro-fluoro-acetyl chloride 、 alkaline earth salt of/the/ methylsulfuric acid
    参考文献:
    名称:
    Swarts, Bulletin de la Societe Chimique de France, 1895, vol. <3>13, p. 992
    摘要:
    DOI:
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文献信息

  • Synthesis of Fluorine‐Containing 3‐Aminocyclopent‐2‐enones via Intramolecular Cyclization
    作者:Elena N. Shaitanova、Igor I. Gerus、Olga A. Balabon、Viktor E. Ivasyshyn、Karen V. Tarasenko、Constantin G. Daniliuc、Günter Haufe
    DOI:10.1002/ejoc.202001218
    日期:2020.12.13
    An optimized protocol for the preparation of fluorine‐containing acyclic enones, which react with secondary amines to form fluorinated 3‐amino‐cyclopent‐2‐enones via 4‐amino‐2,3‐dihydrofuran‐2‐ols was developed. A plausible mechanism is proposed.
    开发了一种优化的制备含氟无环烯酮的方案,该环烯酮与仲胺反应,通过4-氨基-2,3-二氢呋喃-2-醇形成氟化的3-氨基环戊-2-烯酮。提出了一种合理的机制。
  • Kinetics and Mechanism of the Thermal Gas-Phase Oxidation of Tetrachloroethene by Molecular Oxygen in Presence of Trifluoromethylhypofluorite, CF<sub>3</sub>OF
    作者:Joanna Czarnowski
    DOI:10.1524/zpch.1998.203.part_1_2.183
    日期:1998.1.1
    The oxidation of tetrachloroethene by molecular oxygen in presence of CF3OF has been studied at 314.0, 324.2, 334.1 and 344.3 K. The initial pressure of CF3OF was varied between 2.0 and 8.2 Torr, that of CCl2CCl2 between 8.7 and 21.7 Torr, that of O-2 between 33.2 and 730.7 Torr. Several runs were made adding N-2 at pressure Varying between 250.4 and 525.9 Torr. The major products were CCl3C(O)Cl and COCl2. CF3OCCl2C(O)Cl, CCl2FC(O)Cl, CF3OCCl2CCl2F and CCl2FCCl2F were formed in traces. The oxidation is a chain reaction. Its rate increases with total pressure. The following mechanism, where E = CCl2CCl2, R = CCl2FCCl2, CF3OCCl2CCl2 or CCl,3CCl2, R' = CCl2F, CF3OCCl2 or CCl3 and M = effective pressure, explains the experimental results:1) CF3OF+E-->R+CF3O 2) CF3O+E-->R3, 7) R+O-2+M-->RO2+M 4,8) 2RO(2)-->2RO+O-25) RO-->R'C(O)Cl+Cl 6) Cl+E-->CCl3CCl29) CCl3CCl2O-->CCl3C(O)Cl+Cl 10) CCl3CCl2O-->CCl3+COCl211) CCl3+O-2+M-->CCl3O2+M 12)CCl3O2+RO2-->CCl3O+RO+O-213) CCl3O-->COCl2+Cl 14) 2R-->recombination products,15) R+CF3OF-->RF+CF3Ok(9)=(3.0+/-1.4)X10(13)exp(-9.66+/-1 kcal mol(-1)/RT) s(-1).
  • The Mechanism of Fluorination. I. Fluorine Sensitized Oxidation of Trichloro- and Tetrachloroethylene
    作者:William T. Miller、Albert L. Dittman
    DOI:10.1021/ja01593a039
    日期:1956.6
  • Swarts, Bulletin de la Societe Chimique de France, 1895, vol. <3>13, p. 992
    作者:Swarts
    DOI:——
    日期:——
  • New Amorbacides--VI. The Preparation of some N,N'-Disubstituted-N,N'-bis(haloacyl)-1,4-xylylenediamines
    作者:Alexander R. Surrey、J. Richard Mayer
    DOI:10.1021/jm50016a001
    日期:1961.5
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