摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-三氟甲基-4-羟基-8-甲氧基喹啉 | 41192-84-1

中文名称
2-三氟甲基-4-羟基-8-甲氧基喹啉
中文别名
8-甲氧基-4-羟基-2-(三氟甲基)喹啉
英文名称
8-methoxy-2-trifluoromethyl-1H-quinolin-4-one
英文别名
2-trifluoromethyl-4-hydroxy-8-methoxyquinoline;4-hydroxy-8-methoxy-2-trifluoromethylquinoline;8-Methoxy-2-(trifluoromethyl)-4-quinolinol;4-Hydroxy-8-methoxy-2-(trifluoromethyl)quinoline;8-methoxy-2-(trifluoromethyl)-1H-quinolin-4-one
2-三氟甲基-4-羟基-8-甲氧基喹啉化学式
CAS
41192-84-1
化学式
C11H8F3NO2
mdl
MFCD01862071
分子量
243.185
InChiKey
PJTJOLUVQOIHEC-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:
    339.9±37.0 °C(Predicted)
  • 密度:
    1.407±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.181
  • 拓扑面积:
    38.3
  • 氢给体数:
    1
  • 氢受体数:
    6

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 海关编码:
    2933499090

SDS

SDS:abd3617a5db80082010722a2886ff717
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 4-Hydroxy-8-methoxy-2-(trifluoromethyl)quinoline
Synonyms: 8-Methoxy-2-(trifluoromethyl)quinolin-4-ol

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

Section 3. Composition/information on ingredients.
Ingredient name: 4-Hydroxy-8-methoxy-2-(trifluoromethyl)quinoline
CAS number: 41192-84-1

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: C11H8F3NO2
Molecular weight: 243.2

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.

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

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Meshram, H. M.; Chennakesava Reddy, B.; Aravind Kumar, D., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2012, vol. 51, # 9, p. 1411 - 1416,6
    摘要:
    DOI:
  • 作为产物:
    描述:
    邻甲氧基苯胺三氟乙酰乙酸乙酯 在 magnesium sulfate 、 溶剂黄146 、 dowtherm A 作用下, 以 乙醇 为溶剂, 反应 16.5h, 生成 2-三氟甲基-4-羟基-8-甲氧基喹啉
    参考文献:
    名称:
    天然奎宁生物碱启发的新型喹啉衍生物的设计,合成和抗真菌评价
    摘要:
    受奎宁及其类似物的启发,我们设计,合成和评估了两个系列的喹啉小分子化合物(a和2a)和六个系列的喹啉衍生物(3a - f)的抗真菌活性。结果表明,化合物3e和3f系列表现出显着的杀真菌活性。值得注意的是,化合物3f-4(EC 50 = 0.41μg/ mL)和3f-28(EC 50 = 0.55μg/ mL)显示出优异的体外杀真菌活性和对菌核菌的有效体内治疗作用。初步机理研究表明,化合物3f-4和3f-28可能引起细胞膜通透性改变,活性氧的积累,线粒体膜电位的丧失以及有效抑制菌核菌的发芽和形成。这些结果表明,化合物3f-4和3f-28是对抗源自天然产物的核盘菌的新型潜在杀真菌剂。
    DOI:
    10.1021/acs.jafc.9b04224
点击查看最新优质反应信息

文献信息

  • PYRAZOLONE DERIVATIVE AND PDE INHIBITOR CONTAINING THE SAME AS ACTIVE INGREDIENT
    申请人:Kyorin Pharmaceutical Co., Ltd.
    公开号:EP2168960A1
    公开(公告)日:2010-03-31
    It is to provide a novel pyrazolone derivative represented by the following general formula (1), which is useful as a pharmaceutical and has a phosphodiesterase inhibitory action: wherein R1,R2: C1-6 alkyl; R3,R4: H, X, C1-6 alkoxy; Z:O, S; A:AA, BB, wherein AA represents wherein BB represents wherein R5: H, C1-6 alkyl ; R6,R7: C1-6 alkyl.
    提供一种新颖的吡唑酮衍生物, represented by the following general formula (1),该衍生物可用作药物,并具有磷酸二酯酶抑制作用: 其中 R1,R2:C1-6烷基;R3,R4:H,X,C1-6烷氧基;Z:O,S;A:AA,BB,其中AA代表 其中BB代表 其中R5:H,C1-6烷基;R6,R7:C1-6烷基。
  • PYRIDAZINONE DERIVATIVE AND PDE INHIBITOR CONTAINING THE SAME AS ACTIVE INGREDIENT
    申请人:Kyorin Pharmaceutical Co., Ltd.
    公开号:EP2168959A1
    公开(公告)日:2010-03-31
    It is to provide a novel pyridazinone derivative represented by the following general formula (1), which is useful as a pharmaceutical and has a phosphodiesterase inhibitory action: wherein R1 represents H or C1-6 alkyl, each of R2 and R3 represents H, X, C1-6 alkoxy, Z represents O or S, and A represents AA or BB, wherein AA represents: and BB represents: wherein R4 represents H or C1-6 alkyl, and each of R5 and R6 represents C1-6 alkyl.
    提供一种新颖的吡啶并酮衍生物,其通式如下(1),可用作药物,并具有磷酸二酯酶抑制作用: 其中R1代表H或C1-6烷基,R2和R3各自代表H、X、C1-6烷氧基,Z代表O或S,A代表AA或BB,其中AA代表: 而BB代表: 其中R4代表H或C1-6烷基,R5和R6各自代表C1-6烷基。
  • 8-hydroxy-7-substituted quinolines as anti-viral agents
    申请人:Pharmacia & Upjohn Company
    公开号:US06211376B1
    公开(公告)日:2001-04-03
    The present invention provides for 8-hydroxy-7-substituted quinoline compounds such as formula III These compounds are useful as anti-viral agents. Specifically, these compounds have anti-viral activity against the herpes virus, cytomegalovirus (CMV). Many of these compounds are also active against other herpes viruses, such as the varicella zoster virus, the Epstein-Barr virus, the herpes simplex virus and the human herpes virus type 8 (HHV-8).
    本发明提供了8-羟基-7-取代喹啉类化合物,如公式III所示。这些化合物可用作抗病毒剂。具体而言,这些化合物对疱疹病毒、巨细胞病毒(CMV)具有抗病毒活性。许多这些化合物也对其他疱疹病毒具有活性,如痘带状疱疹病毒、爱泼斯坦-巴尔病毒、单纯疱疹病毒和人类疱疹病毒8型(HHV-8)。
  • [EN] 8-HYDROXY-7-SUBSTITUTED QUINOLINES AS ANTI-VIRAL AGENTS<br/>[FR] 8-HYDROXYQUINOLEINES 7-SUBSTITUEES UTILISEES COMME AGENTS ANTIVIRAUX
    申请人:PHARMACIA & UPJOHN COMPANY
    公开号:WO1998011073A1
    公开(公告)日:1998-03-19
    (EN) The present invention provides for 8-hydroxy-7-substituted quinoline compounds such as formula (IA). These compounds are useful as anti-viral agents. Specifically, these compounds have anti-viral activity against the herpes virus, cytomegalovirus (CMV). Many of these compounds are also active against other herpes viruses, such as the varicella zoster virus, the Epstein-Barr virus, the herpes simplex virus and the human herpes virus type 8 (HHV-8).(FR) L'invention concerne des composés de 8-hydroxyquinoléine substituée en 7, représentés par la formule (IA). Ces composés sont utiles comme agents antiviraux. Ils présentent en particulier une activité antivirale contre le virus herpétique cytomégalovirus (CMV). Un grand nombre de ces composés sont également actifs contre d'autres virus herpétiques tels le virus varicelle-zona, le virus Epstein-Barr, le virus herpes simplex et le virus herpétique humain de type 8 (VHH-8).
    本发明提供了8-羟基-7-取代喹啉化合物,例如式(IA)。这些化合物可用作抗病毒剂。具体而言,这些化合物对于疱疹病毒、巨细胞病毒(CMV)具有抗病毒活性。其中许多化合物也对其他疱疹病毒,例如带状疱疹病毒、EB病毒、单纯疱疹病毒和人类疱疹病毒8型(HHV-8)具有活性。
  • Proline derivatives and use thereof as drugs
    申请人:Kitajima Hiroshi
    公开号:US20050245538A1
    公开(公告)日:2005-11-03
    The present invention aims at providing compounds having therapeutic effects due to a DPP-IV inhibitory action, and satisfactory as pharmaceutical products. The present inventors have found that derivatives having a substituent introduced into the γ-position of proline represented by the formula (I) wherein each symbol is as defined in the specification, have a potent DPP-IV inhibitory activity, and completed the present invention by increasing the stability.
    本发明旨在提供具有治疗效果的化合物,其作用是通过DPP-IV的抑制作用,并且作为药物产品具有令人满意的效果。本发明人发现,在丙酸的γ位上引入取代基的衍生物具有强效的DPP-IV抑制活性,并通过增加稳定性完成了本发明。
查看更多