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3-(苄氧基)-6-氟吡嗪 | 870646-05-2

中文名称
3-(苄氧基)-6-氟吡嗪
中文别名
——
英文名称
3-Benzyloxy-6-fluoropyridazine
英文别名
3-(Benzyloxy)-6-fluoropyridazine;3-fluoro-6-phenylmethoxypyridazine
3-(苄氧基)-6-氟吡嗪化学式
CAS
870646-05-2
化学式
C11H9FN2O
mdl
——
分子量
204.204
InChiKey
IWKTXEWKOWHYQW-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):
    2.1
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    35
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    吗啉3-(苄氧基)-6-氟吡嗪 以80.5%的产率得到3-(4-morpholinyl)-6-benzyloxypyridazine
    参考文献:
    名称:
    Synthesis and Herbicidal Evaluation of 3-N-Substituted Amino-6-benzyloxypyridazine Derivatives
    摘要:
    A variety of 3‐N‐substituted amino‐6‐benzyloxypyridazine derivatives were designed and synthesized in satisfactory yields. Their structures were confirmed by IR, 1H‐NMR, and elemental analysis; compound 5j was further determined by X‐ray diffraction crystallography. Their herbicidal activities were evaluated through barnyard grass and rape cup tests in laboratory bioassays. Most of the title compounds 5 displayed moderate herbicidal activities against the dicotyledonous plant Brassica campestris L. The most active compounds in the laboratory were also evaluated in the greenhouse.
    DOI:
    10.1002/jhet.1831
  • 作为产物:
    描述:
    3,6-二氟哒嗪苯甲醇 在 sodium hydroxide 作用下, 以 乙腈 为溶剂, 生成 3-(苄氧基)-6-氟吡嗪
    参考文献:
    名称:
    Synthesis and Herbicidal Evaluation of 3-N-Substituted Amino-6-benzyloxypyridazine Derivatives
    摘要:
    A variety of 3‐N‐substituted amino‐6‐benzyloxypyridazine derivatives were designed and synthesized in satisfactory yields. Their structures were confirmed by IR, 1H‐NMR, and elemental analysis; compound 5j was further determined by X‐ray diffraction crystallography. Their herbicidal activities were evaluated through barnyard grass and rape cup tests in laboratory bioassays. Most of the title compounds 5 displayed moderate herbicidal activities against the dicotyledonous plant Brassica campestris L. The most active compounds in the laboratory were also evaluated in the greenhouse.
    DOI:
    10.1002/jhet.1831
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