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2,5-二溴-4-硝基吡啶 | 221241-31-2

中文名称
2,5-二溴-4-硝基吡啶
中文别名
——
英文名称
2,5-dibromo-4-nitropyridine
英文别名
2,5-Dibromo-4-nitropyridine
2,5-二溴-4-硝基吡啶化学式
CAS
221241-31-2
化学式
C5H2Br2N2O2
mdl
——
分子量
281.891
InChiKey
QQNCRXJHMWJGQK-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:
    283.7±35.0 °C(Predicted)
  • 密度:
    2?+-.0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 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:
    58.7
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933399090
  • 危险性防范说明:
    P261,P280,P301+P312,P302+P352,P305+P351+P338
  • 危险性描述:
    H302,H315,H320,H335

SDS

SDS:754b29e84514f5f3ecff9d0062cb2ba6
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • ANTI-FIBROTIC PYRIDINONES
    申请人:InterMune, Inc.
    公开号:US20140094456A1
    公开(公告)日:2014-04-03
    Disclosed are pyridinone compounds, method for preparing these compounds, and methods for treating fibrotic disorders.
    揭示了吡啶酮化合物,制备这些化合物的方法,以及治疗纤维化疾病的方法。
  • ORGANOMETALLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME
    申请人:Samsung Display Co., Ltd.
    公开号:US20210313524A1
    公开(公告)日:2021-10-07
    An organic light-emitting device includes an emission layer including a first compound represented by Formula 1, a second compound, and a third compound. The first compound may be an organometallic compound that acts as a phosphorescent dopant, and the second and third compounds may form an exciplex. The device may have a low driving voltage, high luminance, high efficiency, and a long lifespan:
    一种有机发光器件包括一个发射层,其中包括由化合物1表示的第一化合物,第二化合物和第三化合物。第一化合物可以是作为磷光掺杂剂的有机金属化合物,第二和第三化合物可以形成一个异质复合物。该器件可能具有低驱动电压、高亮度、高效率和长寿命。
  • Pyrrolopyridine Derivatives
    申请人:Eatherton John Andrew
    公开号:US20070219229A1
    公开(公告)日:2007-09-20
    The present invention relates to novel pyrrolopyridine derivatives, pharmaceutical compositions containing these compounds and their use in the treatment of diseases, particularly pain, which diseases are caused directly or indirectly by an increase or decrease in activity of the cannabinoid receptor.
    本发明涉及新型吡咯吡啶衍生物、含有这些化合物的药物组合物及其在治疗疾病,特别是疼痛方面的用途,这些疾病直接或间接地由大麻素受体活性的增加或减少引起。
  • Pyrrolopyridine derivatives
    申请人:Glaxo Group Limited
    公开号:US07589206B2
    公开(公告)日:2009-09-15
    The present invention relates to novel pyrrolopyridine derivatives, pharmaceutical compositions containing these compounds and their use in the treatment of diseases, particularly pain, which diseases are caused directly or indirectly by an increase or decrease in activity of the cannabinoid receptor.
    本发明涉及一种新的吡咯吡啶衍生物,其中包含这些化合物的药物组合物,以及它们在治疗疾病,特别是由于大麻素受体活性的增加或减少直接或间接引起的疼痛等疾病中的应用。
  • Discovery of 1-[4-(3-Chlorophenylamino)-1-methyl-1<i>H</i>-pyrrolo[3,2-<i>c</i>]pyridin-7-yl]-1-morpholin-4-ylmethanone (GSK554418A), a Brain Penetrant 5-Azaindole CB<sub>2</sub> Agonist for the Treatment of Chronic Pain
    作者:Gerard M. P. Giblin、Andrew Billinton、Michael Briggs、Andrew J. Brown、Iain P. Chessell、Nick M. Clayton、Andrew J. Eatherton、Paul Goldsmith、Carl Haslam、Matthew R. Johnson、William L. Mitchell、Alan Naylor、Alcide Perboni、Brian P. Slingsby、Alex W. Wilson
    DOI:10.1021/jm9009857
    日期:2009.10.8
    We report the synthesis and SAR of a series of novel azaindole CB2 agonists. 6-Azaindole 18 showed activity in an acute pain model but was inactive in a chronic model. 18 is a Pgp substrate with low brain penetration. The template was redesigned, and the resulting 5-azaindole 36 was a potent CB2 agonist with high CNS penetration. This compound was efficacious in the acute model and the chronic joint pain model.
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