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1,1,3,3,3-五氟-2-碘丙-1-烯 | 431-66-3

中文名称
1,1,3,3,3-五氟-2-碘丙-1-烯
中文别名
——
英文名称
2-iodo-1,1,3,3,3-pentafluoropropene
英文别名
2-Iodopentafluoropropene;1,1,3,3,3-pentafluoro-2-iodo-propene;pentafluoro-isopropenyl iodide;pentafluoro-2-iodo-propene;Pentafluor-2-jod-propen;2-Jodo-pentafluoro-propen;2-Iodo-1,1,3,3,3-pentafluoroprop-1-ene;1,1,3,3,3-pentafluoro-2-iodoprop-1-ene
1,1,3,3,3-五氟-2-碘丙-1-烯化学式
CAS
431-66-3
化学式
C3F5I
mdl
——
分子量
257.93
InChiKey
XLJCQUUBIFJNCQ-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:
    44.9±35.0 °C(Predicted)
  • 密度:
    2?+-.0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    5

安全信息

  • 海关编码:
    2903799090

SDS

SDS:ad66a2d1cf023458954dee0a8bd65a8e
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反应信息

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文献信息

  • Reactions of Perfluorinated Alkenyl-, Alkynyl-, Alkyltrifluoroborates, and Selected Hydrocarbon Analogues with the Halogenating Agents Hal2 (Hal = F, Cl, Br), “BrF” (BrF3-Br2 1:1), and ICl
    作者:Vadim V. Bardin、Nicolay Yu. Adonin、Hermann-Josef Frohn
    DOI:10.1002/zaac.201100276
    日期:2012.3
    fluorine (5 %) in 1, 1, 1, 3, 3-pentafluorobutane (PFB) showed only [Bu4N][CF3CF2CF2BF3] as fluorine addition product besides extensive fluorodeboration. Suspensions of the insoluble K[CF2=CFBF3] salt reacted with Cl2 and Br2 in CH2Cl2 giving preferentially products of halogen addition across the C=C bond. In reactions with ICl iododeboration with formation of CF2=CFI occurred besides 1, 2-addition with
    [Bu4N][RBF3] [R = CnF2n+1CF=CF(顺式,反式),CF2=CF,CF2=C(CF3),反式-C4H9CF=CF,反式-C6H5CF=CF,C4H9CH=CH(顺式,反式)的反应、反式)、CF3C≡C 和 C4H9C≡C] 与氯、溴、BrF3 + Br2(相当于“BrF”)和溶液中的 ICl(CH2Cl2、CHCl3、CF3CH2CF2CH3)导致卤素的 1, 2-加成和/或用卤素代替硼(卤代硼化)。[Bu4N][CF3C≡CBF3] 与低于等摩尔量的稀释氟 (5 %) 在 1, 1, 1, 3, 3-五氟丁烷 (PFB) 中的反应表明仅 [Bu4N][CF3CF2CF2BF3] 作为氟加成产物除了广泛的氟硼酸。不溶性 K[CF2=CFBF3] 盐的悬浮液在 CH2Cl2 中与 Cl2 和 Br2 反应,优先生成卤素通过 C=C 键加成的产物。在与 ICl 碘脱硼的反应中,除了
  • Convenient preparation and functionalization of 2-metallated pentafluoropropenes
    作者:Peter A. Morken、Hengyao Lu、Nakamura Akihiro、Donald J. Burton
    DOI:10.1016/s0040-4039(00)92146-4
    日期:1991.1
    The title compounds are prepared by metallation of CF3CH = CF2 with LDA or t-BuLi or by metallation of CF3CBr2CF3 with 2 equivalents of zinc. CF3C(ZnX) = CF2 undergoes halogenation, oxidative dimerization, allylation and acylation reactions.
  • Preparation of .beta.,.beta.-difluoro-.alpha.-(trifluoromethyl)styrenes by palladium-catalyzed coupling of aryl iodides with pentafluoropropen-2-ylzinc reagent
    作者:Peter A. Morken、Donald J. Burton
    DOI:10.1021/jo00057a032
    日期:1993.2
    Substituted aromatic iodides are functionalized by pentafluoropropen-2-ylzinc, CF3C(ZnX)=CF2 (X = Br, I, or CF2=CCF3-), in the presence of Pd(PPh3)4 to give the corresponding arenes in good yields. This is particularly attractive for preparation of title styrenes substituted with groups such as -NO2 or CO2R, which are incompatible with organomagnesium reagents. The best yields of the title styrenes with electron-donating substituents were obtained in DMF. For electron-withdrawing substituents, the best results were achieved in triglyme. A correlation was observed between Hammett sigma constants and F-19 NMR chemical shifts (R = 0.93-0.99, n = 8) and 2J(F-F) coupling constants (R = 0.94, n = 8).
  • Knunjanz et al., Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1958, p. 425;engl.Ausg.S.407
    作者:Knunjanz et al.
    DOI:——
    日期:——
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