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3,3,4,4,5,5,6,6,7,7,8,8,9,9,10-Pentadecafluoro-1,12-diiodo-10-trifluoromethyl-dodecane | 1027379-92-5

中文名称
——
中文别名
——
英文名称
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10-Pentadecafluoro-1,12-diiodo-10-trifluoromethyl-dodecane
英文别名
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10-pentadecafluoro-1,12-diiodo-10-(trifluoromethyl)dodecane
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10-Pentadecafluoro-1,12-diiodo-10-trifluoromethyl-dodecane化学式
CAS
1027379-92-5
化学式
C13H8F18I2
mdl
——
分子量
759.987
InChiKey
JNQXRXWJRPEMJO-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):
    9.2
  • 重原子数:
    33
  • 可旋转键数:
    11
  • 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:
    18

反应信息

  • 作为反应物:
    描述:
    3,3,4,4,5,5,6,6,7,7,8,8,9,9,10-Pentadecafluoro-1,12-diiodo-10-trifluoromethyl-dodecane硫酸 作用下, 生成 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10-Pentadecafluoro-10-trifluoromethyl-dodecane-1,12-diol
    参考文献:
    名称:
    Difunctional Monomers Based on Perfluoropropylene Telomers
    摘要:
    Telomers of perfluoropropylene with alpha,omega-diiodoperfluoroalkanes were converted to branched-chain difunctional condensation monomers. The reaction of ethylene with the telomers gave alpha,omega-bis(iodoethyl)perfluoroalkanes, which were converted to the corresponding diols by reaction with fuming sulfuric acid. The reaction of the branched-chain alpha,omega-bis(iodoethyl)perfluoroalkane a with sodium azide gave the corresponding alpha,omega-bis(azidoethyl)perfluoroalkanes. Hydrogenation of the alpha,omega-bis(azidoethyl)perfluoroalkanes gave diamines. Phosgenation of the amino groups gave diisocyanates.
    DOI:
    10.1021/jo00101a048
  • 作为产物:
    描述:
    乙烯1,8-Diiodoperfluorononane 160.0 ℃ 、2.07 MPa 条件下, 以88%的产率得到3,3,4,4,5,5,6,6,7,7,8,8,9,9,10-Pentadecafluoro-1,12-diiodo-10-trifluoromethyl-dodecane
    参考文献:
    名称:
    Difunctional Monomers Based on Perfluoropropylene Telomers
    摘要:
    Telomers of perfluoropropylene with alpha,omega-diiodoperfluoroalkanes were converted to branched-chain difunctional condensation monomers. The reaction of ethylene with the telomers gave alpha,omega-bis(iodoethyl)perfluoroalkanes, which were converted to the corresponding diols by reaction with fuming sulfuric acid. The reaction of the branched-chain alpha,omega-bis(iodoethyl)perfluoroalkane a with sodium azide gave the corresponding alpha,omega-bis(azidoethyl)perfluoroalkanes. Hydrogenation of the alpha,omega-bis(azidoethyl)perfluoroalkanes gave diamines. Phosgenation of the amino groups gave diisocyanates.
    DOI:
    10.1021/jo00101a048
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文献信息

  • US6084057A
    申请人:——
    公开号:US6084057A
    公开(公告)日:2000-07-04
  • US6451960B1
    申请人:——
    公开号:US6451960B1
    公开(公告)日:2002-09-17
  • US6552161B1
    申请人:——
    公开号:US6552161B1
    公开(公告)日:2003-04-22
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