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4',5'-bis(hydroxymethyl)fluorescein dibenzoate | 1344032-74-1

中文名称
——
中文别名
——
英文名称
4',5'-bis(hydroxymethyl)fluorescein dibenzoate
英文别名
[6'-Benzoyloxy-4',5'-bis(hydroxymethyl)-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl] benzoate
4',5'-bis(hydroxymethyl)fluorescein dibenzoate化学式
CAS
1344032-74-1
化学式
C36H24O9
mdl
——
分子量
600.581
InChiKey
GYJTWDSHMFDJIO-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):
    5.2
  • 重原子数:
    45
  • 可旋转键数:
    8
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    129
  • 氢给体数:
    2
  • 氢受体数:
    9

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
  • 下游产品
    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:
    4',5'-bis(hydroxymethyl)fluorescein dibenzoatebeta-D-半乳糖五乙酸酯三氟化硼乙醚三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 4.0h, 以66%的产率得到
    参考文献:
    名称:
    Studies on the synthesis and the antimicrobial and antioxidant activities of a novel class of fluorescein-based glycosides
    摘要:
    Facile glycosylation of a fluorescein diol derivative with per-O-acetylibenzoyl sugar derivatives using BF3 center dot Et2O catalyst resulted in the formation of the expected glycosides in 54-66% yield. The biological screening of the glycosides against different microbes shows good inhibitory activity. The antioxidant activity of the fluorescein-based glycosides shows remarkable inhibition (IC50 similar to 80%). (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.08.005
  • 作为产物:
    描述:
    4',5'-bis(bromomethyl)fluoresceine dibenzoate碳酸氢钠 作用下, 以 乙腈 为溶剂, 反应 2.0h, 以68%的产率得到4',5'-bis(hydroxymethyl)fluorescein dibenzoate
    参考文献:
    名称:
    Studies on the synthesis and the antimicrobial and antioxidant activities of a novel class of fluorescein-based glycosides
    摘要:
    Facile glycosylation of a fluorescein diol derivative with per-O-acetylibenzoyl sugar derivatives using BF3 center dot Et2O catalyst resulted in the formation of the expected glycosides in 54-66% yield. The biological screening of the glycosides against different microbes shows good inhibitory activity. The antioxidant activity of the fluorescein-based glycosides shows remarkable inhibition (IC50 similar to 80%). (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.08.005
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文献信息

  • US7160732B2
    申请人:——
    公开号:US7160732B2
    公开(公告)日:2007-01-09
  • Studies on the synthesis and the antimicrobial and antioxidant activities of a novel class of fluorescein-based glycosides
    作者:Mani Rajasekar、Raman Jegadeesh、Nanjian Raaman、Thangamuthu Mohan Das
    DOI:10.1016/j.carres.2011.08.005
    日期:2011.11
    Facile glycosylation of a fluorescein diol derivative with per-O-acetylibenzoyl sugar derivatives using BF3 center dot Et2O catalyst resulted in the formation of the expected glycosides in 54-66% yield. The biological screening of the glycosides against different microbes shows good inhibitory activity. The antioxidant activity of the fluorescein-based glycosides shows remarkable inhibition (IC50 similar to 80%). (C) 2011 Elsevier Ltd. All rights reserved.
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