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2-(difluoromethyl)-2-methyl-2,3-dihydro-1H-perimidine

中文名称
——
中文别名
——
英文名称
2-(difluoromethyl)-2-methyl-2,3-dihydro-1H-perimidine
英文别名
2-(Difluoromethyl)-2-methyl-1,3-dihydroperimidine;2-(difluoromethyl)-2-methyl-1,3-dihydroperimidine
2-(difluoromethyl)-2-methyl-2,3-dihydro-1H-perimidine化学式
CAS
——
化学式
C13H12F2N2
mdl
——
分子量
234.248
InChiKey
XKRDDNNLVWQDBH-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):
    4.1
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    24.1
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1,1-二氟丙酮1,8-二氨基萘 在 BF3 monohydrate complex 作用下, 反应 2.0h, 生成 2-(difluoromethyl)-2-methyl-2,3-dihydro-1H-perimidine
    参考文献:
    名称:
    Synthesis of perimidine and 1,5-benzodiazepine derivatives using tamed Brønsted acid, BF3–H2O
    摘要:
    The one pot synthesis of perimidine and 1,5-benzodiazepine derivatives via condensation of aryldiamines with ketones in the presence of BF3-H2O is described. BF3-H2O plays a dual role, as an efficient non-oxidizing Bronsted acid catalyst as well as an effective solvent making the reaction more economic and environmentally safer. The reaction is simple, fast and convenient. (C) 2013 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2013.03.023
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文献信息

  • Synthesis of perimidine and 1,5-benzodiazepine derivatives using tamed Brønsted acid, BF3–H2O
    作者:G.K. Surya Prakash、Farzaneh Paknia、Arjun Narayan、Thomas Mathew、George A. Olah
    DOI:10.1016/j.jfluchem.2013.03.023
    日期:2013.8
    The one pot synthesis of perimidine and 1,5-benzodiazepine derivatives via condensation of aryldiamines with ketones in the presence of BF3-H2O is described. BF3-H2O plays a dual role, as an efficient non-oxidizing Bronsted acid catalyst as well as an effective solvent making the reaction more economic and environmentally safer. The reaction is simple, fast and convenient. (C) 2013 Elsevier B.V. All rights reserved.
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