1-[5-C-(2,3-O-isopropylidene-1,4-anhydro-β-D-erythrofuranosyl)-2-methylfuran]-2,3-dibromo-3-(2,4-dibromophenyl)propan-1-one | 1161838-38-5

• 分子结构分类: 有机化合物 - 有机杂环化合物
• 英文名称: 1-[5-C-(2,3-O-isopropylidene-1,4-anhydro-β-D-erythrofuranosyl)-2-methylfuran]-2,3-dibromo-3-(2,4-dibromophenyl)propan-1-one
• CAS: 1161838-38-5
• 化学式: C₂₁H₂₀Br₄O₅
• 分子量: 672.003
• InChiKey: YMWRYVPYEKVDIJ-DBBPMMMXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.79
• 重原子数：
  30.0
• 可旋转键数：
  5.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  57.9
• 氢给体数：
  0.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  1-[5-C-(2,3-O-isopropylidene-1,4-anhydro-β-D-erythrofuranosyl)-2-methylfuran]-2,3-dibromo-3-(2,4-dibromophenyl)propan-1-one 在 水 、 溶剂黄146 作用下， 反应 2.0h， 以71%的产率得到1-[5-C-(1,4-anhydro-β-D-erythrofuranosyl)-2-methylfuran]-2,3-dibromo-3-(2,4-dibromophenyl)propan-1-one
  参考文献：
  名称：

  C-Furyl glycosides, I: Synthesis and antimicrobial evaluation of C-furyl glycosides and chalcones derived therefrom

  摘要：

  New C-furyl glycosides were synthesized in order to increase the number of compounds screened for antimicrobial activity. The antimicrobial activity showed that the bromo as well as the nitro derivatives were the most active compounds.

  DOI：

  10.1007/s00706-008-0941-1
• 作为产物：
  描述：

  (E)-1-[5-C-(2,3-O-isopropylidene-1,4-anhydro-β-D-erythrofuranosyl)-2-methylfuran]-3-(2,4-dibromophenyl)prop-2-en-1-one 在 溴 作用下， 以 氯仿 为溶剂， 反应 1.5h， 以81%的产率得到1-[5-C-(2,3-O-isopropylidene-1,4-anhydro-β-D-erythrofuranosyl)-2-methylfuran]-2,3-dibromo-3-(2,4-dibromophenyl)propan-1-one
  参考文献：
  名称：

  C-Furyl glycosides, I: Synthesis and antimicrobial evaluation of C-furyl glycosides and chalcones derived therefrom

  摘要：

  New C-furyl glycosides were synthesized in order to increase the number of compounds screened for antimicrobial activity. The antimicrobial activity showed that the bromo as well as the nitro derivatives were the most active compounds.

  DOI：

  10.1007/s00706-008-0941-1