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2-(2'-methylpropyl)-4,6-dimethoxy-1,3,5-triazine

中文名称
——
中文别名
——
英文名称
2-(2'-methylpropyl)-4,6-dimethoxy-1,3,5-triazine
英文别名
2,4-Dimethoxy-6-(2-methylpropyl)-1,3,5-triazine;2,4-dimethoxy-6-(2-methylpropyl)-1,3,5-triazine
2-(2'-methylpropyl)-4,6-dimethoxy-1,3,5-triazine化学式
CAS
——
化学式
C9H15N3O2
mdl
——
分子量
197.237
InChiKey
GJIJCFZYMSFYCC-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):
    2.2
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    57.1
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-氯-4,6-二甲氧基-1,3,5-三嗪三异丁基铝 在 bis-triphenylphosphine-palladium(II) chloride 作用下, 以 乙醚 为溶剂, 反应 2.0h, 以70%的产率得到2-(2'-methylpropyl)-4,6-dimethoxy-1,3,5-triazine
    参考文献:
    名称:
    Organometallic alkylation of 2-chloro-4,6-dimethoxy-1,3,5-triazine: a study
    摘要:
    The reactivity of 2-chloro-4,6-dimethoxy-1,3,5-triazine (1) has been investigated in Pd- or Ni-catalyzed cross-coupling processes with organostannanes, Grignard reagents, organoalanes and organozinc halides. All organometallic reagents considered form new C-C bonds on the heteroaromatic ring and afford the corresponding 2-alkyl-4,6-dimethoxy-1,3,5-triazines in moderate to very good yields. The collected data allows the choice of the alkylating agent as well as the experimental conditions depending on the residue to transfer. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2005.02.085
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文献信息

  • Organometallic alkylation of 2-chloro-4,6-dimethoxy-1,3,5-triazine: a study
    作者:Simona Samaritani、Giovanni Signore、Corrado Malanga、Rita Menicagli
    DOI:10.1016/j.tet.2005.02.085
    日期:2005.5
    The reactivity of 2-chloro-4,6-dimethoxy-1,3,5-triazine (1) has been investigated in Pd- or Ni-catalyzed cross-coupling processes with organostannanes, Grignard reagents, organoalanes and organozinc halides. All organometallic reagents considered form new C-C bonds on the heteroaromatic ring and afford the corresponding 2-alkyl-4,6-dimethoxy-1,3,5-triazines in moderate to very good yields. The collected data allows the choice of the alkylating agent as well as the experimental conditions depending on the residue to transfer. (c) 2005 Elsevier Ltd. All rights reserved.
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