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1,2-二氯-1,1,3,3-五氟丙烷 | 431-86-7

中文名称
1,2-二氯-1,1,3,3-五氟丙烷
中文别名
——
英文名称
1,1,1,3,3-pentafluoro-2,3-dichloropropane
英文别名
AK-225;asahiklin AK-225;2,3-Dichlor-1,1,1,3,3-pentafluor-propan;2,3-dichloro-1,1,1,3,3-pentafluoropropane;1,2-dichloro-1,1,3,3,3-pentafluoro-propane;1,2-Dichlor-1,1,3,3,3-pentafluor-propan;HCFC-225da;1,2-Dichloro-1,1,3,3,3-pentafluoropropane
1,2-二氯-1,1,3,3-五氟丙烷化学式
CAS
431-86-7
化学式
C3HCl2F5
mdl
MFCD00054727
分子量
202.939
InChiKey
XAHBEACGJQDUPF-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:
    50°C
  • 密度:
    1,56 g/cm3
  • 物理描述:
    1,2-dichloro-1,1,3,3,3-pentafluoropropane is a colorless odorless liquid. Nonflammable.

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    5

安全信息

  • 危险等级:
    IRRITANT-HARMFUL, OZONE DEPLETER
  • 危险品标志:
    Xi
  • 安全说明:
    S23,S36/37/39
  • 危险类别码:
    R20/21/22,R59
  • 海关编码:
    2903791090
  • 危险品运输编号:
    UN 3082

SDS

SDS:96be424e5795def1acf4aa577cfd684f
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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

反应信息

  • 作为反应物:
    描述:
    1,2-二氯-1,1,3,3-五氟丙烷 在 0.5% palladium on alumina 氢气 作用下, 生成 1,1,3,3,3-五氟-1-丙烯
    参考文献:
    名称:
    Method of dechlorinating organic compounds comprising vicinal chlorides
    摘要:
    提供了一种选择性制备2-氯五氟丙烯的方法,包括在氢气和贵金属催化剂存在下对1,2,2-三氯-1,1,3,3,3-五氟丙烷进行催化脱氯。还提供了一种使用钯/硫酸钡催化剂对邻氯代有机化合物进行脱氯的方法。
    公开号:
    US07473810B1
  • 作为产物:
    参考文献:
    名称:
    Some Fluorinated Derivatives of Propane1
    摘要:
    DOI:
    10.1021/ja01186a013
  • 作为试剂:
    描述:
    氯乙酰氯苯酚1,2-二氯-1,1,3,3-五氟丙烷 作用下, 反应 9.0h, 以96%的产率得到氯乙酸苯酯
    参考文献:
    名称:
    METHOD FOR PRODUCING CARBONATE COMPOUND AND METHOD FOR PRODUCING AROMATIC POLYCARBONATE
    摘要:
    本发明涉及一种制备碳酸盐化合物的方法,包括以下步骤:第一步,将由以下化学式(1)表示的化合物与由以下化学式(21)或以下化学式(22)表示的化合物反应,以获得含有碳酸盐化合物的反应混合物;第二步,将含有碳酸盐化合物的反应混合物与强碱性化合物接触,其中R1代表一价有机基团,R2代表二价有机基团。
    公开号:
    US20150152037A1
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文献信息

  • Reaction of bistrifluoromethylaminosulphenyl chloride with fluoro-olefins and hexafluorobut-2-yne under free-radical conditions
    作者:Colin F. Service、Anthony E. Tipping
    DOI:10.1016/s0022-1139(00)84027-0
    日期:1982.3
    Reaction of bistrifluoromethylaminosulphenyl chloride with unsymmetrical fluoro-olefins in daylight or under photochemical conditions gives both possible 1:1 adducts (ca. 1:1 ratio) arising from homolytic fission of the SCl bond. Addition to octafluorobut-2-ene and hexafluorobut-2-yne gives mixtures of the syn- and anti- adducts.
    在日光下或在光化学条件下,双三氟甲基氨基磺酰氯与不对称氟代烯烃的反应产生了SCl键的均裂裂化产生的两种可能的1:1加合物(比例约为1:1)。除八氟丁-2-烯和六氟丁-2-炔外,可得到正加合物和反加合物的混合物。
  • [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、氯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是在存在氯氟化催化剂的情况下产生的,该催化剂包括ZnCr2O4/结晶α-铬氧化物组合物、经氟化剂处理过的ZnCr2O4/结晶α-铬氧化物组合物、锌卤化物/α-铬氧化物组合物和/或经氟化剂处理过的锌卤化物/α-铬氧化物组合物。
  • The addition of free radicals to unsaturated systems. Part XV. Further investigation of the direction of radical addition to chloro-1,1-difluoroethylene
    作者:R. Gregory、R. N. Haszeldine、A. E. Tipping
    DOI:10.1039/j39680003020
    日期:——
    reaction of chloro-1,1-difluoroethylene with trifluoroiodomethane gives a 92% yield of the 1 : 1 adducts 3-chloro-1,1,1,2,2-pentafluoro-3-iodopropane and 2-chloro-1,1,1,3,3-pentafluoro-3-iodopropane in the ratio 92 : 8. The major by-product is 1,1-difluoroiodoethylene. Reaction at 225° gives a low yield of the same 1 : 1 adducts (ratio 98 : 2). Irradiation of 3-chloro-1,1,1,2,2-pentafluoro-3-iodopropane gives
    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。
  • [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-铬氧化物组成的氟化催化剂的存在下产生的,该氟化催化剂经过氟化剂处理的ZnCr2O4 / 晶体α-铬氧化物组成,锌卤化物 / α-铬氧化物组成和/或经过氟化剂处理的锌卤化物/α-铬氧化物组成。
  • 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,其中包括铬、氧和金作为必要的成分元素。在组成物中金的量为总铬和金的量的约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氟分布(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)通过将氢氧化铵(水合氨)加入至含有至少三摩尔硝酸盐的可溶性金盐和可溶性铬盐的水溶液中,该水溶液中铬的摩尔数为溶液中铬的摩尔数,并且金含量为约总金和铬含量的0.05原子%至约10原子%,以形成含有共沉淀固体的水溶液混合物;(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)用可溶性金盐的溶液浸渍固体铬氧化物,(b)干燥步骤a中制备的浸渍的铬氧化物;以及可选地,(c)煅烧所干燥的固体。第三种制备方法包括(a)蒸发铬(VI)氧化物和可溶性金盐的水溶液以形成固体;(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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