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Tert-butyl 4-(furan-2-ylmethylcarbamoyl)piperazine-1-carboxylate | 1207981-80-3

中文名称
——
中文别名
——
英文名称
Tert-butyl 4-(furan-2-ylmethylcarbamoyl)piperazine-1-carboxylate
英文别名
——
Tert-butyl 4-(furan-2-ylmethylcarbamoyl)piperazine-1-carboxylate化学式
CAS
1207981-80-3
化学式
C15H23N3O4
mdl
——
分子量
309.365
InChiKey
BBUJWLPHFFWXFJ-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):
    0.8
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    75
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    Tert-butyl 4-(furan-2-ylmethylcarbamoyl)piperazine-1-carboxylate盐酸 作用下, 以 1,4-二氧六环 为溶剂, 反应 4.0h, 生成
    参考文献:
    名称:
    Antiplasmodial activity of piperazine sulfonamides
    摘要:
    A high-throughput screening program identified two piperazine sulfonamides with activity against Plasmodium falciparum. Both screening positives had three structural features with potential liabilities: furanyl, thiourea and nitrophenyl groups. The furan could be replaced with no loss of activity, replacement of the nitrophenyl led to some loss of activity, and any attempt to replace the thiourea led to a significant decrease in activity, which implicates this reactive functional group's role in the antiplasmodial activity of this compound class. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.10.130
  • 作为产物:
    参考文献:
    名称:
    Antiplasmodial activity of piperazine sulfonamides
    摘要:
    A high-throughput screening program identified two piperazine sulfonamides with activity against Plasmodium falciparum. Both screening positives had three structural features with potential liabilities: furanyl, thiourea and nitrophenyl groups. The furan could be replaced with no loss of activity, replacement of the nitrophenyl led to some loss of activity, and any attempt to replace the thiourea led to a significant decrease in activity, which implicates this reactive functional group's role in the antiplasmodial activity of this compound class. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.10.130
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