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cesium heptafluoroisopropoxide | 13994-52-0

中文名称
——
中文别名
——
英文名称
cesium heptafluoroisopropoxide
英文别名
Cesium;1,1,1,2,3,3,3-heptafluoropropan-2-olate
cesium heptafluoroisopropoxide化学式
CAS
13994-52-0
化学式
C3F7O*Cs
mdl
——
分子量
317.927
InChiKey
FWSYIBMRSWEHMU-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):
    -1.86
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    23.1
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    cesium heptafluoroisopropoxide2-溴苯乙酮乙二醇二甲醚 为溶剂, 反应 24.0h, 以3.79 g的产率得到phenyl(heptafluoroisopropyloxymethyl)ketone
    参考文献:
    名称:
    Efficient synthesis of 5′-fluoroalkoxythiazoles via α-bromo-α-fluoroalkoxyacetophenones Hantzsch type cyclization with thioureas or thioamides
    摘要:
    Novel alpha-fluoroalkoxyacetophenones were synthesized by addition of the readily available 2,2-dimethoxy-2-phenylethanol to fluoroolefins. alpha-Bromination yielded alpha-bromo-alpha-fluoroalkoxyacetophenones, which on treatment with thioureas or thioamides gave thiazoles with fluoroalkoxy groups at the 5'-position by the Hantzsch-type cyclization. This provides a versatile methodology for the construction of heterocycles from aliphatic fluoroalkoxy containing building blocks. (C) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2012.01.005
  • 作为产物:
    描述:
    六氟丙酮 在 cesium fluoride 作用下, 以 二乙二醇二甲醚 为溶剂, 20.0 ℃ 、100.0 kPa 条件下, 生成 cesium heptafluoroisopropoxide
    参考文献:
    名称:
    헵타플루오로이소프로필옥시 테트라플루오로 프로파노일 플루오라이드의 제조방법
    摘要:
    This text appears to be a technical description related to a patent for a method of producing heptafluoroisopropoxy tetrafluoropropionyl fluoride.
    公开号:
    KR102026794B1
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文献信息

  • Gubanov, V. A.; Tyul'ga, G. M.; Solodkaya, I. G., Journal of Organic Chemistry USSR (English Translation), 1984, vol. 20, p. 444 - 448
    作者:Gubanov, V. A.、Tyul'ga, G. M.、Solodkaya, I. G.、Sherman, M. A.
    DOI:——
    日期:——
  • New Electrophilic Reaction of Perfluoroalkylethylenes. Synthesis and Some Reactions of 1-Halo-1,1,2-trihydroperfluoroalkenes-2
    作者:V. A. Petrov
    DOI:10.1021/jo00116a031
    日期:1995.6
    Perfluoroalkylethylenes, R(f)CH=CH2, react with chlorosulfonic acid in the presence of TaF5 or NbF5 catalyst to form allyl chlorides, Z-R(f)CF=CHCH2Cl. These chlorides, or their corresponding bromides, also can be made by the BF3-catalyzed reaction of R(f)CH=CH2 with HCl or HBr in anhydrous HF. The allylic chlorine in the newly synthesized compounds Z-R(f)CF=CHCH2Cl can be easily replaced by reaction with nucleophiles such as I-, Br-, HO-, or (CF3)(2)CFO-.
  • 헵타플루오로이소프로필옥시 테트라플루오로 프로파노일 플루오라이드의 제조방법
    申请人:KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY 한국화학연구원(319980077651)
    公开号:KR102026794B1
    公开(公告)日:2019-09-30
    본 발명은 헵타플루오로이소프로필옥시 테트라플루오로 프로파노일 플루오라이드의 제조방법에 관한 것으로, 본 발명에 따른 헵타플루오로이소프로필옥시 테트라플루오로 프로파노일 플루오라이드 제조방법은, 반응물의 반복적인 교차 투입 방법을 통하여, 생성물로의 전환율을 현저히 향상시키는 유용한 효과가 달성되고, 제조 과정 중에 사용되었던 헵타플루오로아이소프로폭사이드 금속염을 반복 재사용할 수 있는 이점이 있는 바, 연속식 생산 공정이 가능하고, 고순도, 고수율의 헵타플루오로이소프로필옥시 테트라플루오로 프로파노일 플루오라이드 제조가 가능한 유용한 효과가 있다. 또한, 본 발명의 제조방법으로 제조된 헵타플루오로이소프로필옥시 테트라플루오로 프로파노일 플루오라이드는, 말단기를 비닐에테르 또는 에테르로 변환시켜 고분자 중합의 공단량체, 희석제, 세정제 및 코팅제 등으로 제공될 수 있는 바, 유용하다.
    This text appears to be a technical description related to a patent for a method of producing heptafluoroisopropoxy tetrafluoropropionyl fluoride.
  • Efficient synthesis of 5′-fluoroalkoxythiazoles via α-bromo-α-fluoroalkoxyacetophenones Hantzsch type cyclization with thioureas or thioamides
    作者:Taras M. Sokolenko、Yulia A. Davydova、Yurii L. Yagupolskii
    DOI:10.1016/j.jfluchem.2012.01.005
    日期:2012.4
    Novel alpha-fluoroalkoxyacetophenones were synthesized by addition of the readily available 2,2-dimethoxy-2-phenylethanol to fluoroolefins. alpha-Bromination yielded alpha-bromo-alpha-fluoroalkoxyacetophenones, which on treatment with thioureas or thioamides gave thiazoles with fluoroalkoxy groups at the 5'-position by the Hantzsch-type cyclization. This provides a versatile methodology for the construction of heterocycles from aliphatic fluoroalkoxy containing building blocks. (C) 2012 Elsevier B.V. All rights reserved.
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