摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

5-phenyl-2-(4-vinyl-phenyl)-2H-tetrazole | 37571-42-9

中文名称
——
中文别名
——
英文名称
5-phenyl-2-(4-vinyl-phenyl)-2H-tetrazole
英文别名
2-(4-Ethenylphenyl)-5-phenyltetrazole
5-phenyl-2-(4-vinyl-phenyl)-2<i>H</i>-tetrazole化学式
CAS
37571-42-9
化学式
C15H12N4
mdl
——
分子量
248.287
InChiKey
QIPWEHLUNHVRKW-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):
    4.2
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    43.6
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • Preparation of Functional Polymers
    申请人:Matyjaszewski Krzyszlof
    公开号:US20070244265A1
    公开(公告)日:2007-10-18
    The process of the present invention is directed toward conducting highly selective, high yield post polymerization reactions on polymers to prepare functionalized polymers. An embodiment of the present invention comprises conducting click chemistry reactions on polymers. Preferably, the polymers were prepared by controlled polymerization processes. Therefore, embodiments of the present invention comprise processes for the preparation of polymers comprising conducting a click chemistry reaction on a functional group attached to a polymer, wherein the polymer has a molecular weight distribution of less than 2.0. The functional polymers may be prepared by converting an attached functional unit on the polymer thereby providing site specific functional materials, site specific functional materials comprising additional functionality, or chain extended functional materials. Embodiments of the process of the present invention include functionalization reactions, chain extensions reactions, to form mock copolymer linking reactions, and attaching side chains to form graft copolymers, for example.
    本发明的过程旨在对聚合物进行高选择性,高产率的后聚合反应,以制备功能化聚合物。本发明的一种实施例包括在聚合物上进行点击化学反应。最好的情况是,这些聚合物是通过受控聚合过程制备的。因此,本发明的实施例包括制备聚合物的过程,其中包括在连接到聚合物的功能基团上进行点击化学反应,其中聚合物的分子量分布小于2.0。可以通过转化聚合物上的连接功能单元来制备功能性聚合物,从而提供定位特异性的功能材料,包括具有附加功能的定位特异性功能材料,或链延长的功能材料。本发明的过程实施例包括功能化反应,链延伸反应,形成模拟共聚物连接反应,以及连接侧链以形成接枝共聚物等。
  • PREPARATION OF FUNCTIONAL POLYMERS
    申请人:Matyjaszewski Krzysztof
    公开号:US20110060107A1
    公开(公告)日:2011-03-10
    The process of the present invention is directed toward conducting highly selective, high yield post polymerization reactions on polymers to prepare functionalized polymers. An embodiment of the present invention comprises conducting click chemistry reactions on polymers. Preferably, the polymers were prepared by controlled polymerization processes. Therefore, embodiments of the present invention comprise processes for the preparation of polymers comprising conducting a click chemistry reaction on a functional group attached to a polymer, wherein the polymer has a molecular weight distribution of less than 2.0. The functional polymers may be prepared by converting an attached functional unit on the polymer thereby providing site specific functional materials, site specific functional materials comprising additional functionality, or chain extended functional materials. Embodiments of the process of the present invention include functionalization reactions, chain extensions reactions, to form block copolymer linking reactions, and attaching side chains to form graft copolymers, for example.
    本发明的过程旨在对聚合物进行高度选择性和高收率的后聚合反应,以制备功能化聚合物。本发明的一种实施例包括在聚合物上进行点击化学反应。最好的情况是,这些聚合物是通过受控聚合过程制备的。因此,本发明的实施例包括制备聚合物的过程,其中在连接到聚合物上的功能基团上进行点击化学反应,其中聚合物的分子量分布小于2.0。这些功能化聚合物可以通过转换聚合物上的附加功能单元来制备,从而提供特定位置的功能材料,包括具有附加功能的特定位置的功能材料或链延伸功能材料。本发明的过程实施例包括功能化反应、链延长反应、形成块共聚物连接反应和附加侧链以形成嫁接共聚物等。
  • PARTICLES COMPRISING AMPHIPHILIC COPOLYMERS, HAVING A CROSS-LINKED SHELL DOMAIN AND AN INTERIOR CORE DOMAIN, USEFUL FOR PHARMACEUTICAL AND OTHER APPLICATIONS
    申请人:G.D. Searle & Co.
    公开号:EP0907666A1
    公开(公告)日:1999-04-14
  • RESPONSIVE MICROGEL AND METHODS RELATED THERETO
    申请人:SUPRATEK PHARMA, INC.
    公开号:EP1478403A1
    公开(公告)日:2004-11-24
  • US7795355B2
    申请人:——
    公开号:US7795355B2
    公开(公告)日:2010-09-14
查看更多