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[1,1'-binaphthalene]-2,2',8,8'-tetraol

中文名称
——
中文别名
——
英文名称
[1,1'-binaphthalene]-2,2',8,8'-tetraol
英文别名
2.8.2'.8'-Tetraoxy-dinaphthyl-(1.1');[1,1']Binaphthyl-2,8,2',8'-tetraol;8-(2,8-Dihydroxynaphthalen-1-yl)naphthalene-1,7-diol;8-(2,8-dihydroxynaphthalen-1-yl)naphthalene-1,7-diol
[1,1'-binaphthalene]-2,2',8,8'-tetraol化学式
CAS
——
化学式
C20H14O4
mdl
——
分子量
318.329
InChiKey
PPBFNYKIABMSKK-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):
    4.6
  • 重原子数:
    24
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    80.9
  • 氢给体数:
    4
  • 氢受体数:
    4

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:
    [1,1'-binaphthalene]-2,2',8,8'-tetraol 在 [N,N'-bis(salicylidene)ethane-1,2-diaminato]cobalt(II) 、 氧气 作用下, 以 乙腈 为溶剂, 反应 15.5h, 以50%的产率得到(±)-naphtho[1,8-bc]naphtho[1',8':3,4,5]furo[2,3-d]furan-5,12-dione
    参考文献:
    名称:
    Selective Oxidation of 8,8′-Hydroxylated Binaphthols to Bis-spironaphthalenones or Binaphtho-para- and Binaphtho-ortho-quinones
    摘要:
    The selective oxidation of a series of functionalized 8,8'-hydroxylated binaphthols to binaphtho-para- and binaphtho-ortho-quinones has been realized using either a Co-salen catalyst or ortho-iodoxybenzoic acid. A unique spirocyclic bis-spironaphthalenone was also obtained in good yield via a phenyliodonium diacetate promoted oxidative dearomatization.
    DOI:
    10.1021/ol302195e
  • 作为产物:
    参考文献:
    名称:
    Morgan; Vining, Journal of the Chemical Society, 1921, vol. 119, p. 1710
    摘要:
    DOI:
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文献信息

  • SECONDARY BATTERY
    申请人:NOMURA Masayoshi
    公开号:US20160268607A1
    公开(公告)日:2016-09-15
    Provided is a secondary battery that includes an electrode active material including an organic compound represented by the following General Formula 1. Ar—(OH) n In the General Formula 1, Ar denotes at least one selected from the group consisting of 1,1-binaphthalene, anthracene, triphenylene, tetraphenylene, and pyrene, and is optionally substituted with a substituent. The substituent of Ar is at least one selected from the group consisting of an OH group, a carbonyl group produced through oxidization of the OH group, an alkyl group containing 3 or less carbon atoms, a halogen atom, and an amino group. n denotes an integer in a range of from 2 through 8.
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