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8-溴-6-氟喹啉 | 22960-18-5

中文名称
8-溴-6-氟喹啉
中文别名
——
英文名称
8-bromo-6-fluoroquinoline
英文别名
——
8-溴-6-氟喹啉化学式
CAS
22960-18-5
化学式
C9H5BrFN
mdl
——
分子量
226.048
InChiKey
DOINWPRJXLNEBB-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:
    294.9±20.0 °C(Predicted)
  • 密度:
    1.647±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    12.9
  • 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,P280,P301+P312,P302+P352,P305+P351+P338
  • 危险性描述:
    H302,H315,H320,H335
  • 储存条件:
    室温

SDS

SDS:d590cc029e948ad5ae45c67038fe85dc
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 8-Bromo-6-fluoroquinoline
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 8-Bromo-6-fluoroquinoline
CAS number: 22960-18-5

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.

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.

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.

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:

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.

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: C9H5BrFN
Molecular weight: 226.0

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, hydrogen fluoride, hydrogen bromide.

Section 11. Toxicological information
No data.

Section 12. Ecological information
No data.

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.

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

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.


SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

  • 作为反应物:
    描述:
    8-溴-6-氟喹啉 在 [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 、 palladium diacetate 、 potassium carbonateR-(+)-1,1'-联萘-2,2'-双二苯膦sodium t-butanolate 作用下, 以 甲醚甲苯 为溶剂, 反应 40.0h, 生成 N-(tert-butyl)-6-fluoro-5-tosylquinolin-8-amine
    参考文献:
    名称:
    钌催化的N-烷基-8-氨基喹啉的远程C5-磺化。
    摘要:
    对位置选择性远程CH功能化的方法学的需求不断增长。我们在此报告了8-氨基喹啉衍生物的钌催化的远程C5-选择性磺化。使用不同的取代底物可获得中等至高收率。该催化体系表现出高的区域选择性以及良好的官能团耐受性。机理研究支持一个根本途径。提出了双功能钌催化循环。
    DOI:
    10.1039/c9ob01357a
  • 作为产物:
    描述:
    2-溴-4-氟苯胺甘油ferrous(II) sulfate heptahydrate甲烷磺酸sodium 3-nitrobenzenesulfonate 作用下, 反应 20.0h, 以33%的产率得到8-溴-6-氟喹啉
    参考文献:
    名称:
    双功能有机催化剂通过卤代反应诱导8-芳基喹啉中的轴向手性。
    摘要:
    轴向手性杂二芳基的对映选择性合成是通过3-(喹啉-8-基)苯酚的芳香亲电卤化与双功能有机催化剂来控制的,该双功能有机催化剂在连续的卤化过程中控制分子的构象。轴向手性喹啉衍生物很少以对映选择性催化方式合成,通过溴化反应可得到中等至良好的对映选择性,类似的方案也可实现对映选择性碘化。此外,这种催化反应允许通过使用单邻位取代的底物进行对映选择性控制,从而实现了高对映选择性下带有两个不同卤素基团的8-芳基喹啉衍生物的不对称合成。
    DOI:
    10.1002/chem.201701707
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文献信息

  • Piperazine-piperidine antagonists and agonists of the 5-HT1A receptor
    申请人:Asselin Magda
    公开号:US20070027160A1
    公开(公告)日:2007-02-01
    The present invention relates to novel piperazine-piperidine compounds. The compounds are useful as 5-HT 1A binding agents, particularly as 5-HT 1A receptor antagonists and agonists. These compounds are useful in treating central nervous system disorders, such as cognition disorders, anxiety disorders, depression and sexual dysfunction.
    本发明涉及新型哌嗪-哌啶化合物。这些化合物可用作5-HT1A结合剂,特别是作为5-HT1A受体拮抗剂和激动剂。这些化合物在治疗中枢神经系统疾病方面很有用,如认知障碍、焦虑症、抑郁症和性功能障碍。
  • Quinoline synthesis by improved Skraup–Doebner–Von Miller reactions utilizing acrolein diethyl acetal
    作者:Ginelle A. Ramann、Bryan J. Cowen
    DOI:10.1016/j.tetlet.2015.09.145
    日期:2015.11
    Miller reaction providing access to various quinoline products. The straightforward procedure utilizes acrolein diethyl acetal as a three-carbon annulation partner with aniline substrates in a monophasic, organic solvent-free reaction medium. Differentially substituted aniline precursors were found to be compatible with the reaction conditions and the corresponding quinoline products are isolated in
    已经开发了一种强大的合成方法,以改进古老的Skraup–Doebner–Von Miller反应,从而可以使用各种喹啉产品。简单的方法是在单相,无有机溶剂的反应介质中,将丙烯醛二乙缩醛与苯胺基质一起用作三碳环化伙伴。发现差异取代的苯胺前体与反应条件相容,并且以中等至良好的产率分离出相应的喹啉产物。
  • [EN] TETRALIN AND TETRAHYDROQUINOLINE COMPOUNDS AS INHIBITORS OF HIF-2ALPHA<br/>[FR] COMPOSÉS DE TÉTRALINE ET DE TÉTRAHYDROQUINOLINE UTILISÉS EN TANT QU'INHIBITEURS DE HIF-2 ALPHA
    申请人:ARCUS BIOSCIENCES INC
    公开号:WO2021188769A1
    公开(公告)日:2021-09-23
    Compounds that inhibit HIF-2a, and compositions containing the compound(s) and methods for synthesizing the compounds, are described herein. Also described are the use of such compounds and compositions for the treatment of a diverse array of diseases disorders, and conditions, including cancer- and immune-related disorders that are mediated, at least in part, by HIF-2a.
    抑制HIF-2a的化合物,以及包含该化合物的方法和合成化合物的方法都在这里描述。还描述了使用这些化合物和组合物治疗多种疾病、障碍和状况,包括至少部分由HIF-2a介导的癌症和免疫相关障碍。
  • BENZOFURANYL- AND BENZOTHIENYL- PIPERAZINYL QUINOLINES AND METHODS OF THEIR USE
    申请人:Venkatesan Aranapakam Mudumbai
    公开号:US20090054454A1
    公开(公告)日:2009-02-26
    Benzofuranyl- and benzothienyl-piperzinyl quinoline derivatives and compositions containing such compounds are disclosed. Methods of using benzofuranyl- and benzothienyl-piperzinyl quinoline derivatives and compositions containing such composition in the treatment and/or prevention of serotonin-related disorders, such as depression and anxiety, are also disclosed. In addition, processes for the preparation of benzofuranyl- and benzothienyl-piperzinyl quinoline derivatives are disclosed.
    本专利揭示了苯并呋喃基和苯并噻吩基哌嗪喹啉衍生物以及含有这些化合物的组合物。还揭示了使用苯并呋喃基和苯并噻吩基哌嗪喹啉衍生物以及含有这种组合物在治疗和/或预防与5-羟色胺相关的疾病,如抑郁症和焦虑症的方法。此外,还揭示了制备苯并呋喃基和苯并噻吩基哌嗪喹啉衍生物的方法。
  • [EN] NITROGENOUS HETEROCYCLIC DERIVATIVES AND THEIR APPLICATION IN DRUGS<br/>[FR] DÉRIVÉS HÉTÉROCYCLIQUES AZOTÉS ET LEUR APPLICATION DANS DES MÉDICAMENTS
    申请人:SUNSHINE LAKE PHARMA CO LTD
    公开号:WO2015090232A1
    公开(公告)日:2015-06-25
    The present invention relates to the field of medicine, provided herein are novel nitrogenous heterocyclic compounds, their preparation methods and their uses as drugs, especially for treatment and prevention of tissue fibrosis. Also provided herein are pharmaceutically acceptable compositions comprising the nitrogenous heterocyclic compounds and the uses of the compositions in the treatment of human or animal tissue fibrosis, especially for human or animal renal interstitial fibrosis, glomerular sclerosis, liver fibrosis, pulmonary fibrosis, IPF, peritoneal fibrosis, myocardial fibrosis, dermatofibrosis, postsurgical adhesion, benign prostatic hyperplasia, skeletal muscle fibrosis, scleroderma, multiple sclerosis, pancreatic fibrosis, cirrhosis, myosarcoma, neurofibroma, pulmonary interstitial fibrosis, diabetic nephropathy, alzheimer disease or vascular fibrosis.
    本发明涉及医学领域,提供了新颖的含氮杂环化合物,其制备方法以及作为药物的用途,特别是用于治疗和预防组织纤维化。本文还提供了包含这些含氮杂环化合物的药用可接受组合物,以及这些组合物在治疗人类或动物组织纤维化方面的用途,特别是用于人类或动物肾间质纤维化、肾小球硬化、肝纤维化、肺纤维化、IPF、腹膜纤维化、心肌纤维化、皮肤纤维化、术后粘连、良性前列腺增生、骨骼肌纤维化、硬皮病、多发性硬化、胰腺纤维化、肝硬化、肌肉肉瘤、神经纤维瘤、肺间质纤维化、糖尿病肾病、阿尔茨海默病或血管纤维化。
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