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1-(6-己基吡啶-2-基)哌嗪 | 120144-99-2

中文名称
1-(6-己基吡啶-2-基)哌嗪
中文别名
——
英文名称
1-(6-hexyl-2-pyridinyl)piperazine
英文别名
Piperazine, 1-(6-hexyl-2-pyridinyl)-;1-(6-hexylpyridin-2-yl)piperazine
1-(6-己基吡啶-2-基)哌嗪化学式
CAS
120144-99-2
化学式
C15H25N3
mdl
——
分子量
247.384
InChiKey
JHZPBMMAYNSZEG-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

物化性质

  • 沸点:
    124-126 °C(Press: 0.1 Torr)
  • 密度:
    0.990±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    18
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    28.2
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:6db3ab77a32f973b3eb3e8b7ab9e37ea
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反应信息

  • 作为产物:
    描述:
    仲辛酮sodium 作用下, 以 乙醚正丁醇 为溶剂, 反应 48.0h, 生成 1-(6-己基吡啶-2-基)哌嗪
    参考文献:
    名称:
    6-Alkyl-N,N-disubstituted-2-pyridinamines as anticonvulsant agents
    摘要:
    The anticonvulsant effect of a series of 6-alkyl-N,N-disubstituted-2-pyridinamines is described. An investigation was carried out to optimize the anticonvulsant activity and reduce behavioral side effects in this series. Three compounds (7, 8, 10; Table I) were selected from initial screening for a more complete pharmacological evaluation. While each of these compounds was a potent anticonvulsant agent with ED50 values from 5 to 10 mg/kg, the activity was accompanied by significant behavioral side effects including decreased spontaneous locomotion, ataxia, and ptosis.
    DOI:
    10.1021/jm00126a015
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文献信息

  • PAVIA, MICHAEL R.;TAYLOR, CHARLES P.;LOBBESTAEL, SANDRA J., J. MED. CHEM., 32,(1989) N, C. 1237-1242
    作者:PAVIA, MICHAEL R.、TAYLOR, CHARLES P.、LOBBESTAEL, SANDRA J.
    DOI:——
    日期:——
  • 6-Alkyl-N,N-disubstituted-2-pyridinamines as anticonvulsant agents
    作者:Michael R. Pavia、Charles P. Taylor、Sandra J. Lobbestael
    DOI:10.1021/jm00126a015
    日期:1989.6
    The anticonvulsant effect of a series of 6-alkyl-N,N-disubstituted-2-pyridinamines is described. An investigation was carried out to optimize the anticonvulsant activity and reduce behavioral side effects in this series. Three compounds (7, 8, 10; Table I) were selected from initial screening for a more complete pharmacological evaluation. While each of these compounds was a potent anticonvulsant agent with ED50 values from 5 to 10 mg/kg, the activity was accompanied by significant behavioral side effects including decreased spontaneous locomotion, ataxia, and ptosis.
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