8-甲氧基喹啉 | 938-33-0

• 物质功能分类: 医药中间体 - 喹啉类化合物
• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 中文名称: 8-甲氧基喹啉
• 英文名称: 8-methoxyquinoline
• CAS: 938-33-0
• 化学式: C₁₀H₉NO
• mdl: MFCD00957068
• 分子量: 159.188
• InChiKey: ZLKGGEBOALGXJZ-UHFFFAOYSA-N

物化性质

• 熔点：
  38-41℃
• 沸点：
  282°C(lit.)
• 密度：
  1.0340
• 保留指数：
  1524;259.8

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  22.1
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2933499090
• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H315,H319,H335
• 储存条件：
  | 0-10°C |

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 8-Methoxyquinoline
Synonyms:

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Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

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Section 3. Composition/information on ingredients.
Ingredient name: 8-Methoxyquinoline
CAS number: 938-33-0

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Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

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Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

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Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

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Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels.
Storage:

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Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

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Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C10H9NO
Molecular weight: 159.2

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Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides.

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Section 11. Toxicological information
No data.

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Section 12. Ecological information
No data.

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Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

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Section 14. Transportation information
Non-harzardous for air and ground transportation.

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Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  8-甲氧基喹啉 在 盐酸 、 水 、 苯胺 作用下， 生成 8-羟基喹啉
  参考文献：
  名称：

  DE583705

  摘要：

  公开号：
• 作为产物：
  描述：

  3-碘-8-甲氧基喹啉 在 tris-(dibenzylideneacetone)dipalladium(0) 、 四丁基氯化铵 、 sodium benzenesulfonate 、 potassium carbonate 、 2-二环己膦基-2'-(N,N-二甲胺)-联苯 作用下， 以 N-甲基吡咯烷酮 为溶剂， 反应 15.0h， 生成 8-甲氧基喹啉
  参考文献：
  名称：

  Palladium-catalyzed desulfitative arylation of 3-haloquinolines with arylsulfinates

  摘要：

  3-Haloquinolines can be functionalized via a palladium-catalyzed desulfitative coupling of arylsulfinates. This method tolerates substitution upon the aromatic ring and shows good selectivity toward variously substituted aromatic rings. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2013.01.018

文献信息

• Substituted benzazoles and methods of their use as inhibitors of Raf kinase
  申请人：——

  公开号：US20040122237A1

  公开（公告）日：2004-06-24

  New substituted benz-azole compounds, compositions and methods of inhibition of Raf kinase activity in a human or animal subject are provided. The new compounds compositions may be used either alone or in combination with at least one additional agent for the treatment of a Raf kinase mediated disorder, such as cancer.

  提供了新的替代苯唑化合物、组合物和抑制人类或动物主体中Raf激酶活性的方法。这些新化合物组合物可以单独使用，也可以与至少一种额外药物结合，用于治疗由Raf激酶介导的疾病，如癌症。
• PROTEIN KINASE INHIBITORS
  申请人：Sheppard S. George

  公开号：US20070203143A1

  公开（公告）日：2007-08-30

  Compounds that inhibit protein kinases, compositions containing the compounds and methods of treating diseases using the compounds are disclosed.

  抑制蛋白激酶的化合物、含有这些化合物的组合物以及利用这些化合物治疗疾病的方法被披露。
• [EN] LUMINESCENT DIAZABENZIMIDAZOLE CARBENE METAL COMPLEXES<br/>[FR] COMPLEXES DIAZABENZIMIDAZOLE CARBÈNE-MÉTAL LUMINESCENTS
  申请人：BASF SE

  公开号：WO2015014835A1

  公开（公告）日：2015-02-05

  The present invention relates to metal-carbene complexes of the general formula (I), where variable M is Ir or Pt and that are characterized by variable R being a group of formula (a). The complexes are used in organic electronic devices, especially OLEDs (Organic Light-Emitting Diodes), illuminating elements, stationary visual display units and in material layers as emitter, charge transport material and/or charge or exiton blocker.

  本发明涉及通式（I）的金属-卡宾配合物，其中变量M是Ir或Pt，并且其特征在于变量R是具有结构式（a）的基团。这些配合物用于有机电子设备，特别是OLED（有机发光二极管）、照明元件、固定视觉显示单元，以及作为发射体、载流子传输材料和/或载流子或激子阻挡层的材料层中。
• Remote site-selective C–H activation directed by a catalytic bifunctional template
  作者：Zhipeng Zhang、Keita Tanaka、Jin-Quan Yu

  DOI：10.1038/nature21418

  日期：2017.3

  In chemical syntheses, the activation of carbon–hydrogen (C–H) bonds converts them directly into carbon–carbon or carbon–heteroatom bonds without requiring any prior functionalization. C–H activation can thus substantially reduce the number of steps involved in a synthesis. A single specific C–H bond in a substrate can be activated by using a ‘directing’ (usually a functional) group to obtain the desired

  在化学合成中，碳-氢 (C-H) 键的活化将它们直接转化为碳-碳或碳-杂原子键，无需任何事先的功能化。因此，C-H 活化可以大大减少合成中涉及的步骤数。可以通过使用“定向”（通常是官能团）基团来激活底物中的单个特定 C-H 键，从而选择性地获得所需的产物。由于所讨论的 C-H 键与导向基团的距离以及底物的形状，这种 C-H 活化反应的适用性会受到严重限制，但已经开发了几种方法来克服这些限制。在这样一种方法中，通过使用共价连接的 U 形模板，已经利用对官能团和底物 C-H 键之间的远端和几何关系的理解来实现元选择性 C-H 激活。然而，在没有合适的官能团来连接它的情况下，这个模板的化学计量安装是不可行的。在这里，我们报告了一种催化双功能腈模板的设计，该模板通过可逆配位而不是共价键结合杂环底物。与该模板协调的两个金属中心具有不同的作用：一个可逆地锚定催化剂附近的底物，另一个切割远程 C-H 键。使用这种策略，我们演示了远程、
• [EN] OXAZOLIDINONE ANTIBACTERIAL AGENTS<br/>[FR] AGENTS ANTIBACTERIENS OXAZOLIDINONE
  申请人：PHARMACIA & UPJOHN CO LLC

  公开号：WO2005082897A1

  公开（公告）日：2005-09-09

  The present invention relates to novel amidoxime and amidine oxazolidinones of formula I , wherein R2, Y1, Y 2, Y3, X, W, G and U are as defined herein in the specification. The compounds of the present invention have potent activities against gram-positive bacteria.

  本发明涉及公式I的新型酰胺肟和酰胺噁唑啉，其中R2、Y1、Y2、Y3、X、W、G和U如本说明书中所定义。本发明的化合物对革兰氏阳性细菌具有强大的活性。

表征谱图