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2-bromo-3-nitropyridin-4-ol | 31872-56-7

中文名称
——
中文别名
——
英文名称
2-bromo-3-nitropyridin-4-ol
英文别名
2-Brom-3-nitro-4-pyridinol;2-bromo-3-nitro-1H-pyridin-4-one
2-bromo-3-nitropyridin-4-ol化学式
CAS
31872-56-7
化学式
C5H3BrN2O3
mdl
——
分子量
218.994
InChiKey
PFVGRSGRDMHUOP-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):
    1.1
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    74.9
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

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文献信息

  • Dipole moment in relation to hydrogen receptor histamine antagonist activity for cimetidine analogs
    作者:Rodney C. Young、Graham J. Durant、John C. Emmett、C. Robin Ganellin、Michael J. Graham、Robert C. Mitchell、H. Douglas Prain、Michael L. Roantree
    DOI:10.1021/jm00151a007
    日期:1986.1
    The activities of a series of H2 receptor histamine antagonists structurally related to cimetidine (1) have been compared to investigate the effect of replacing the cyanoguanidine moiety by other neutral, dipolar groups. Antagonist activity, as measured in vitro on the histamine-stimulated guinea pig right atrium, was found to be very sensitive to relatively minor structural changes. Differences in H2 antagonist activity are accounted for by dipole moment orientation and lipophilicity and are rationalized in terms of an optimum requirement for alignment of a hydrogen-bonding moiety in the antagonist with respect to the receptor and desolvation effects at the receptor. The most active compound in the series is the 2-amino-3-nitropyrrole derivative 5, which combines a near-optimal dipole orientation with high lipophilicity.
  • 헤테로고리 화합물 및 이를 이용한 유기발광소자
    申请人:LT Materials Co.,Ltd. 엘티소재주식회사(120060104982) Corp. No ▼ 110111-3251082BRN ▼104-81-94599
    公开号:KR20160007438A
    公开(公告)日:2016-01-20
    본 명세서는 신규한 헤테로고리 화합물 및 이를 이용한 유기발광소자에 관한 것이다.
    本规范针对新型杂环化合物及其在有机发光器件中的应用。
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