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2-氯-1,1,3,3,3-五氟丙-1-烯 | 2804-50-4

中文名称
2-氯-1,1,3,3,3-五氟丙-1-烯
中文别名
——
英文名称
2-chloropentafluoropropene
英文别名
2-Chlor-1,1,3,3,3-pentafluor-propen;2-chloro-1,1,3,3,3-pentafluoropropene;2-chloro-1,1,3,3,3-pentafluoroprop-1-ene
2-氯-1,1,3,3,3-五氟丙-1-烯化学式
CAS
2804-50-4
化学式
C3ClF5
mdl
MFCD00042592
分子量
166.478
InChiKey
YTCHAEAIYHLXBK-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

  • 熔点:
    -130°C
  • 沸点:
    5-6°C
  • 密度:
    1,5 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    5

安全信息

  • 危险等级:
    GAS, TOXIC
  • 危险品标志:
    F,T
  • 安全说明:
    S23,S38
  • 危险类别码:
    R23
  • 海关编码:
    2903799090
  • 危险品运输编号:
    UN 3162

SDS

SDS:625c59d2fccae754236dec4938ec0351
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-氯-1,1,3,3,3-五氟丙-1-烯 在 potassium fluoride 、 formamide 作用下, 生成 2-氯-1,1,1,3,3,3-六氟丙烷
    参考文献:
    名称:
    Substitution and Addition Reactions of the Fluoroölefins. IV.1 Reactions of Fluoride Ion with Fluoroölefins2,3
    摘要:
    DOI:
    10.1021/ja01497a028
  • 作为产物:
    参考文献:
    名称:
    向不饱和体系中添加自由基。第十五部分。进一步研究向1,1-二氟氯乙烯中自由基加成的方向
    摘要:
    氯-1,1-二氟乙烯与三氟碘甲烷的光化学反应产生92:%的1:1加合物3-氯-1,1,1,2,2-五氟-3-碘丙烷和2-氯-1,1的产率为92%比例为92:8的1,1,3,3-五氟-3-碘丙烷。主要副产物为1,1-二氟碘乙烯。在225°反应时,相同的1:1加合物的收率低(比率98:2)。辐照3-氯-1,1,1,2,2-五氟-3-碘丙烷是主要产物三氟碘甲烷,三氟氯甲烷和1,1-二氟碘乙烯。溴化氢与氯-1,1-二氟乙烯的光化学反应导致仅形成1-溴-2-氯-1,1-二氟乙烷。
    DOI:
    10.1039/j39680003020
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文献信息

  • Stable fluorinated allylic cations as intermediates in reaction of electrophilic alkenylation of fluoroethylens
    作者:G.G. Belen'kii、M.V. Galachov、V.A. Petrov、L.S. German、V.I. Bachmutov
    DOI:10.1016/s0022-1139(00)83337-0
    日期:1985.8
    It has been found that perfluoropropylene, perfluoroisobutylene and analogous substances react with SbF5 to form stable allylic cations, which have been observed by NMR 13C, 19F spectra.
    已经发现全氟丙烯全氟异丁烯和类似物质与SbF 5反应形成稳定的烯丙基阳离子,已通过NMR 13 C,19 F光谱观察到。
  • [EN] PROCESS FOR THE PREPARATION OF 1,1,1,3,3-PENTAFLUOROPROPANE AND 1,1,1,2,3-PENTAFLUOROPROPANE<br/>[FR] PROCEDE D'ELABORATION DE 1,1,1,3,3-PENTAFLUOROPROPANE ET DE 1,1,1,2,3-PENTAFLUOROPROPANE
    申请人:DU PONT
    公开号:WO2005037743A1
    公开(公告)日:2005-04-28
    A process is disclosed for the manufacture of CF3CH2CHF2 and CF3CHFCH2F. The process involves (a) reacting hydrogen fluoride, chlorine, and at least one halopropene of the formula CX3CCl=CClX (where each X is independently F or Cl) to produce a product including both CF3CCl2CClF2 and CF3CClFCCl2F; (b) reacting CF3CCl2CClF2 and CF3CClFCCl2F produced in (a) with hydrogen to produce a product including both CF3CH2CHF2, and CF3CHFCH2F; and (c) recovering CF3CH2CHF2 and CF3CHFCH2F from the product produced in (b). In (a), the CF3CCl2CClF2 and CF3CClFCCl2F are produced in the presence of a chlorofluorination catalyst including a ZnCr2O4/crystalline α-chromium oxide composition, a ZnCr2O4/crystalline α-chromium oxide composition which has been treated with a fluorinating agent, a zinc halide/α-chromium oxide composition and/or a zinc halide/α-chromium oxide composition which has been treated with a fluorinating agent.
    揭示了一种制备CF3CH2CHF2和CF3CHFCH2F的工艺。该工艺涉及:(a)反应氢氟酸和至少一种具有分子式CX3CCl=CClX的卤代丙烯,其中每个X独立地为F或Cl,以产生包括CF3CCl2CClF2和CF3CClFCCl2F的产物;(b)将(a)中产生的CF3CCl2CClF2和CF3CClFCCl2F与氢反应,以产生包括CF3CH2CHF2和CF3CHFCH2F的产物;(c)从(b)中产生的产物中回收CF3CH2CHF2和CF3CHFCH2F。在(a)中,CF3CCl2CClF2和CF3CClFCCl2F是在存在化催化剂的情况下产生的,该催化剂包括ZnCr2O4/结晶α-氧化物组合物、经化剂处理过的ZnCr2O4/结晶α-氧化物组合物、卤化物/α-氧化物组合物和/或经化剂处理过的卤化物/α-氧化物组合物。
  • Method of dechlorinating organic compounds comprising vicinal chlorides
    申请人:Honeywell International Inc.
    公开号:US07473810B1
    公开(公告)日:2009-01-06
    Provided is a method for selectively preparing 2-chloropentafluoropropene comprising catalytic dechlorination of 1,2,2-trichloro-1,1,3,3,3-pentafluoropropane in the presence of hydrogen and a noble metal catalyst. Also provided is method for dechlorinating a vicinal chloride substituted organic compound using a palladium/barium sulfate catalyst.
    提供了一种选择性制备2-丙烯的方法,包括在氢气贵金属催化剂存在下对1,2,2-三-1,1,3,3,3-五丙烷进行催化脱。还提供了一种使用/硫酸钡催化剂对邻代有机化合物进行脱的方法。
  • [EN] PROCESS FOR THE PREPARATION OF 1,1,1,3,3-PENTAFLUOROPROPANE AND 1,1,1,3,3,3-HEXAFLUOROPROPANE<br/>[FR] PROCEDE D'ELABORATION DE 1,1,1,3,3-PENTAFLUOROPROPANE ET DE 1,1,1,3,3,3-HEXAFLUOROPROPANE
    申请人:DU PONT
    公开号:WO2005037744A1
    公开(公告)日:2005-04-28
    A process for the manufacture of CF3CH2CHF2 and CF3CH2CF3 is disclosed. The process involves (a) reacting HF and at least one halopropene of the formula CX3CCl=CClX (where each X is independently F or Cl) to produce a product including both CF3CCl=CF2 and CF3CHClCF3; (b) reacting CF3CCl=CF2 and CF3CHClCF3 produced in (a) with hydrogen to produce a product including both CF3CH2CHF2 and CF3CH2CF3; and (c) recovering CF3CH2CHF2 and CF3CH2CF3 from the product produced in (b). In (a), the CF3CCl=CF2 and CF3CHClCF3 are produced in the presence of a fluorination catalyst including a ZnCr2O4/crystalline α-chromium oxide composition, a ZnCr2O4/crystalline α-chromium oxide composition which has been treated with a fluorinating agent, a zinc halide/α-chromium oxide composition and/or a zinc halide/α-chromium oxide composition which has been treated with a fluorinating agent.
    揭示了一种制造CF3CH2CHF2和CF3CH2CF3的过程。该过程包括(a)反应HF和至少一种卤代丙烯的公式CX3CCl = CClX(其中每个X独立地为F或Cl)以产生包括CF3CCl = CF2和CF3CHClCF3的产物; (b)将在(a)中产生的CF3CCl = CF2和CF3CHClCF3与氢反应以产生包括CF3CH2CHF2和CF3CH2CF3的产物; 和(c)从(b)中产生的产物中回收CF3CH2CHF2和CF3CH2CF3。在(a)中,CF3CCl = CF2和CF3CHClCF3是在包括ZnCr2O4 / 晶体α-氧化物组成的化催化剂的存在下产生的,该化催化剂经过化剂处理的ZnCr2O4 / 晶体α-氧化物组成,卤化物 / α-氧化物组成和/或经过化剂处理的卤化物/α-氧化物组成。
  • Compositions containing chromium, oxygen and gold, their preparation, and their use as catalysts and catalyst precursors
    申请人:Rao Velliyur Nott Mallikarjuna
    公开号:US20080207964A1
    公开(公告)日:2008-08-28
    A catalyst composition is disclosed that includes chromium, oxygen, and gold as essential constituent elements. The amount of gold in the composition is from about 0.05 atom % to about 10 atom % based on the total amount of chromium and gold. Also disclosed is a process for changing the fluorine distribution (i.e., content and/or arrangement) in a hydrocarbon or halogenated hydrocarbon in the presence of the catalyst composition; and methods for preparing said catalyst composition. One preparation method involves; (a) co-precipitating a solid by adding ammonium hydroxide (aqueous ammonia) to an aqueous solution of a soluble gold salt and a soluble chromium salt that contains at least three moles of nitrate per mole of chromium in the solution and has a gold content of from about 0.05 atom % to about 10 atom % of the total content of gold and chromium in the solution to form an aqueous mixture containing co-precipitated solid; (b) drying the co-precipitated solid formed in (a); and (c) calcining the dried solid formed in (b) in an atmosphere containing at least 10% oxygen by volume. Another preparation method involves (a) impregnating solid chromium oxide with a solution of a soluble gold salt, (b) drying the impregnated chromium oxide prepared in (a); and optionally, (c) calcining the dried solid. A third preparation method involves (a) evaporating an aqueous solution of chromium(VI) oxide and a soluble gold salt to form a solid; (b) drying the solid formed in (a); and (c) calcining the dried solid formed in (b) in an atmosphere containing at least 10% oxygen by volume.
    揭示了一种催化剂组成物,其中包括、氧和作为必要的成分元素。在组成物中的量为总的量的约0.05原子%至约10原子%。还公开了一种在催化剂组成物存在下改变碳氢化合物或卤代碳氢化合物中分布(即含量和/或排列)的过程;以及制备该催化剂组成物的方法。其中一种制备方法包括:(a)通过将氢氧化)加入至含有至少三摩尔硝酸盐的可溶性盐和可溶性盐的溶液中,该溶液中的摩尔数为溶液中的摩尔数,并且含量为约总含量的0.05原子%至约10原子%,以形成含有共沉淀固体的溶液混合物;(b)干燥步骤a中形成的共沉淀固体;以及(c)在至少10%体积氧气的气氛中煅烧步骤b中形成的干燥固体。另一种制备方法包括(a)用可溶性盐的溶液浸渍固体氧化物,(b)干燥步骤a中制备的浸渍的氧化物;以及可选地,(c)煅烧所干燥的固体。第三种制备方法包括(a)蒸发(VI)氧化物和可溶性盐的溶液以形成固体;(b)干燥步骤a中形成的固体;以及(c)在至少10%体积氧气的气氛中煅烧步骤b中形成的干燥固体。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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