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3,3-di(2',4'-dihydroxyphenyl)phthalide | 1428447-91-9

中文名称
——
中文别名
——
英文名称
3,3-di(2',4'-dihydroxyphenyl)phthalide
英文别名
3,3-bis(2,4-dihydroxyphenyl)-2-benzofuran-1-one
3,3-di(2',4'-dihydroxyphenyl)phthalide化学式
CAS
1428447-91-9
化学式
C20H14O6
mdl
——
分子量
350.328
InChiKey
OCJHXJHCQCPIND-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):
    3.1
  • 重原子数:
    26
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    107
  • 氢给体数:
    4
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    苯酐间苯二酚 在 aluminum (III) chloride 、 sodium chloride 作用下, 反应 0.75h, 以11%的产率得到1,3-二羥蒽醌
    参考文献:
    名称:
    Synthesis of damnacanthal, a naturally occurring 9,10-anthraquinone and its analogues, and its biological evaluation against five cancer cell lines
    摘要:
    Damnacanthal and nordamnacanthal, two naturally occurring 9,10-anthraquinones, and their analogues were synthesized. Cytotoxic activity against five cancer cell lines was evaluated using MTT assay. 2-Bromomethyl-1,3-dimethoxyanthraquinone was found to display the highest activity against all cell lines with IC50 range of 2-8 mu M. Structure-activity relationship (SAR) assessment was considered to rationalise the cytotoxic effect. Bromomethyl group at position C-2 of the anthraquinone was found to be important in exerting cytotoxic activity of this class of compounds. The presence of the flanking methoxyl or hydroxyl groups at C-1 and C-3 also contributes to this activity. Finally, the antioxidant effect of these compounds was evaluated. MTT assay was used to measure the cytotoxicity against different cancer cell lines. Antioxidant activity was measured by FTC and TBA methods. Only two anthraquinones, damnacanthal and nordamnacanthal, were found to be antioxidative.
    DOI:
    10.1007/s00044-012-0197-5
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文献信息

  • Photoresist underlayer film-forming composition and pattern forming process
    申请人:Shin-Etsu Chemical Co., Ltd.
    公开号:EP2813889A2
    公开(公告)日:2014-12-17
    In lithography, a composition comprising a novolak resin comprising recurring units derived from a phenolphthalein, Phenol Red, Cresolphthalein, Cresol Red, or Thymolphthalein is used to form a photoresist underlayer film. The underlayer film is strippable in alkaline water, without causing damage to ion-implanted Si substrates or SiO2 substrates.
    在光刻技术中,一种包含由酚酞酚红、甲酚酞甲酚红百里酚酞递归单元组成的树脂的组合物用于形成光阻底层膜。底层膜可在碱中剥离,不会对离子注入的基底或二氧化硅基底造成损坏。
  • Underlayer film-forming composition and pattern forming process
    申请人:SHIN-ETSU CHEMICAL CO., LTD.
    公开号:US10228621B2
    公开(公告)日:2019-03-12
    In lithography, a composition comprising a novolak resin comprising recurring units derived from a phenolphthalein, Phenol Red, Cresolphthalein, Cresol Red, or Thymolphthalein is used to form a photoresist underlayer film. The underlayer film is strippable in alkaline water, without causing damage to ion-implanted Si substrates or SiO2 substrates.
    在光刻技术中,一种包含由酚酞酚红、甲酚酞甲酚红百里酚酞递归单元组成的树脂的组合物用于形成光阻底层膜。底层膜可在碱中剥离,不会对离子注入的基底或二氧化硅基底造成损坏。
  • UNDERLAYER FILM-FORMING COMPOSITION AND PATTERN FORMING PROCESS
    申请人:SHIN-ETSU CHEMICAL CO., LTD.
    公开号:US20140363955A1
    公开(公告)日:2014-12-11
    In lithography, a composition comprising a novolak resin comprising recurring units derived from a phenolphthalein, Phenol Red, Cresolphthalein, Cresol Red, or Thymolphthalein is used to form a photoresist underlayer film. The underlayer film is strippable in alkaline water, without causing damage to ion-implanted Si substrates or SiO 2 substrates.
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