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(1,1,2,3,3,3-hexafluoro-propyl)-propyl ether | 357-99-3

中文名称
——
中文别名
——
英文名称
(1,1,2,3,3,3-hexafluoro-propyl)-propyl ether
英文别名
(1,1,2,3,3,3-Hexafluor-propyl)-propyl-aether;1,1,1,2,3,3-Hexafluoro-3-propoxypropane
(1,1,2,3,3,3-hexafluoro-propyl)-propyl ether化学式
CAS
357-99-3
化学式
C6H8F6O
mdl
——
分子量
210.119
InChiKey
RALMJSSSISMLSH-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:
    92-93 °C
  • 密度:
    1.260 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

点击查看最新优质反应信息

文献信息

  • PROCESS FOR PRODUCING 1,1,1,3,3-PENTAFLUOROPROPANE
    申请人:Daikin Industries, Ltd.
    公开号:EP1231195A1
    公开(公告)日:2002-08-14
    In a process for producing 1,1,1,3,3-pentafluoropropane which comprises a liquid-phase reaction step for fluorination of 1,1,1,3,3-pentahalopropane (wherein at least one of halogen atoms is not fluorine) with HF in the presence of an antimony pentahalide catalyst in a reactor to obtain a reaction mixture comprising 1,1,1,3,3-pentafluoropropane and the antimony pentahalide catalyst, the fluorination is conducted at a reaction temperature less than 50 °C.
    在一种生产 1,1,1,3,3-五氟丙烷的工艺中,包括一个液相反应步骤,在五卤 化锑催化剂存在下,将 1,1,1,3,3-五氟丙烷(其中至少一个卤素原子不是氟)与氢氟酸 在反应器中进行氟化反应,得到一种反应混合物,其中包括 1、1,1,3,3-五氟丙烷和五卤化锑催化剂的反应混合物,氟化反应在低于 50 °C 的反应温度下进行。
  • METHOD FOR PRODUCING FLUORINE-CONTAINING CARBOXYLIC ACID ESTER
    申请人:Central Glass Company, Limited
    公开号:EP2161249A1
    公开(公告)日:2010-03-10
    [Task] It is to provide a production method that the target fluorine-containing carboxylic acid ester can be obtained from a fluorine-containing ether by a one-step reaction, that a complicated step and a troublesome operation are not necessary, and that an excessive energy is not consumed. [Solving Means] A fluorine-containing carboxylic acid ester represented by the general formula R1HCFCOOR2 is produced by reacting a fluorine-containing ether represented by the general formula R1HCFCF2OR2 (R1 represents either of a fluorine atom and a C1-4 perfluoroalkyl group, and R2 represents a monovalent organic group) with water in the presence of a solid catalyst.
    [任务]提供一种生产方法,它可以通过一步反应从含氟醚中获得目标含氟羧酸酯,不需要复杂的步骤和麻烦的操作,也不会消耗过多的能量。 [解决方法]通式 R1HCFCOOR2 所代表的含氟羧酸酯是由通式 R1HCFCF2OR2 所代表的含氟醚(R1 代表氟原子和 C1-4 全氟烷基中的任一个,R2 代表一价有机基团)在固体催化剂存在下与水反应制得的。
  • Process for producing 1,1,1,3,3-pentafluoropropane
    申请人:Daikin Industries, Ltd.
    公开号:US20040162451A1
    公开(公告)日:2004-08-19
    In a process for producing 1,1,1,3,3-pentafluoropropane which has a liquid-phase reaction step for fluorination of 1,1,1,3,3-pentahalopropane (wherein at least one of halogen atoms is not fluorine) with HF in the presence of antimony pentahalide catalyst in a reactor to obtain a reaction mixture comprising 1,1,1,3,3-pentafluoropropane and the antimony pentahalide catalyst, the fluorination is conducted at a reaction temperature less than 50° C.
    一种生产 1,1,1,3,3-五氟丙烷的工艺,其液相反应步骤是在五卤化锑催化剂存在下,在反应器中将 1,1,1,3,3-五氟丙烷(其中至少有一个卤素原子不是氟)与氢氟酸进行氟化反应,得到一种反应混合物,该混合物包括 1、1,1,3,3-五氟丙烷和五卤化锑催化剂的反应混合物,氟化反应在低于 50°C 的反应温度下进行。
  • METHOD FOR PURIFYING 1,1,1,3,3-PENTAFLUOROPROPANE
    申请人:DAIKIN INDUSTRIES, LIMITED
    公开号:EP0921109B1
    公开(公告)日:2002-01-23
  • Method for Producing Fluorine-Containing Carboxylic Acid Ester
    申请人:Kondo Takeshi
    公开号:US20100197957A1
    公开(公告)日:2010-08-05
    [Task] It is to provide a production method that the target fluorine-containing carboxylic acid ester can be obtained from a fluorine-containing ether by a one-step reaction, that a complicated step and a troublesome operation are not necessary, and that an excessive energy is not consumed. [Solving Means] A fluorine-containing carboxylic acid ester represented by the general formula R 1 HCFCOOR 2 is produced by reacting a fluorine-containing ether represented by the general formula R 1 HCFCF 2 OR 2 (R 1 represents either of a fluorine atom and a C 1-4 perfluoroalkyl group, and R 2 represents a monovalent organic group) with water in the presence of a solid catalyst.
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