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6,13,17,24,31,35-Hexatert-butyl-38,39,41,43-tetraoxa-2,10,20,28-tetrazaundecacyclo[27.7.1.13,36.14,8.19,12.111,15.118,21.122,26.127,30.033,37.019,42]tetratetraconta-1(37),2,4,6,8(44),9,11(42),12,14,16,18,20,22(40),23,25,27,29,31,33,35-icosaene-40,44-diol | 1240601-85-7

中文名称
——
中文别名
——
英文名称
6,13,17,24,31,35-Hexatert-butyl-38,39,41,43-tetraoxa-2,10,20,28-tetrazaundecacyclo[27.7.1.13,36.14,8.19,12.111,15.118,21.122,26.127,30.033,37.019,42]tetratetraconta-1(37),2,4,6,8(44),9,11(42),12,14,16,18,20,22(40),23,25,27,29,31,33,35-icosaene-40,44-diol
英文别名
——
6,13,17,24,31,35-Hexatert-butyl-38,39,41,43-tetraoxa-2,10,20,28-tetrazaundecacyclo[27.7.1.13,36.14,8.19,12.111,15.118,21.122,26.127,30.033,37.019,42]tetratetraconta-1(37),2,4,6,8(44),9,11(42),12,14,16,18,20,22(40),23,25,27,29,31,33,35-icosaene-40,44-diol化学式
CAS
1240601-85-7
化学式
C60H64N4O6
mdl
——
分子量
937.191
InChiKey
DCWPTZPYVUPQSF-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):
    17.8
  • 重原子数:
    70
  • 可旋转键数:
    6
  • 环数:
    11.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    145
  • 氢给体数:
    2
  • 氢受体数:
    10

文献信息

  • CATHODE CATALYST FOR AIR SECONDARY BATTERY AND AIR SECONDARY BATTERY
    申请人:Koshino Nobuyoshi
    公开号:US20140066290A1
    公开(公告)日:2014-03-06
    The present invention provides a cathode catalyst for an air secondary cell having both excellent oxygen reduction activity and excellent water oxidation activity, and an air secondary cell that uses the catalyst. The present invention relates to a cathode catalyst for an air secondary cell in which the catalyst contains a polynuclear metal complex.
    本发明提供了一种空气二次电池的阴极催化剂,具有优异的氧还原活性和优异的氧化活性,并且使用该催化剂的空气二次电池。本发明涉及一种空气二次电池的阴极催化剂,其中该催化剂包含多核属配合物。
  • RING COMPOUND
    申请人:Iwata Masatoshi
    公开号:US20120021897A1
    公开(公告)日:2012-01-26
    A compound represented by the following formula (1): wherein, Y 1 , Y 2 , Y 3 and Y 4 represent a group represented by any of the above formulae; P 1 , P 2 , P 3 and P 4 are an atomic group required for forming an aromatic heterocyclic ring; P 5 and P 6 are an atomic group required for forming an aromatic ring; Z 1 and Z 2 represent OR α , —SR α or —NR α 2 , wherein R α represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms; Q 1 and Q 2 represent a direct bond or a linking group; a P 1 -containing ring and a P 2 -containing ring are bonded to form Q 1 -containing fused structure; a P 3 -containing ring and a P 4 -containing ring are bonded to form Q 2 -containing fused structure; can be used as a ligand of a metal complex, and the metal complex is useful for a catalyst.
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