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5-bromoquinolin-8-ol

  • Name 5-bromoquinolin-8-ol
  • CAS 1198-14-7
  • Purity 99%
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Product Details

Quality Factory Supply 99% Pure 5-bromoquinolin-8-ol 1198-14-7 with Efficient Delivery

  • Molecular Formula: C9H6BrNO
  • Molecular Weight: 224.057
  • Vapor Pressure: 9.07E-06mmHg at 25°C 
  • Melting Point: 127 °C 
  • Refractive Index: 1.717 
  • Boiling Point: 362.7 °C at 760 mmHg 
  • PKA: 3.77±0.10(Predicted) 
  • Flash Point: 173.2 °C 
  • PSA: 33.12000 
  • Density: 1.705 g/cm3 
  • LogP: 2.70290 

5-bromoquinolin-8-ol(Cas 1198-14-7) Usage

General Description

5-Bromoquinolin-8-ol is a chemical compound with a molecular formula C9H6BrNO. It is a yellow crystalline solid that is soluble in organic solvents. 5-bromoquinolin-8-ol is used in the synthesis of pharmaceuticals and agrochemicals. It is also used as a building block in the production of various organic molecules. 5-Bromoquinolin-8-ol has potential applications in medicinal chemistry and drug discovery due to its structural features and biological activities. It is an important intermediate in the formation of various biologically active compounds and is therefore used in the development of new drugs and pharmaceutical products.

InChI:InChI=1/C9H6BrNO/c10-7-3-4-8(12)9-6(7)2-1-5-11-9/h1-5,12H

1198-14-7 Relevant articles

-

Beimer,Fernando

, p. 1003 (1969)

-

-

Prasad et al.

, p. 1251 (1965)

-

-

Chakrabarty et al.

, p. 238 (1967)

-

Visible light-induced mono-bromination of arenes with BrCCl3

Fan, Jiali,Wei, Qiancheng,Zhu, Ershu,Gao, Jing,Cheng, Xiamin,Lu, Yongna,Loh, Teck-Peng

supporting information, p. 5977 - 5980 (2021/06/18)

A highly efficient and regioselective br...

Hydroxyquinolinyl metal organic small molecule cooperation compound material grafted with perylene diimide and aromatic groups, preparation method and applications thereof

-

Paragraph 0030-0033, (2020/03/06)

The invention discloses a hydroxyquinoli...

A general method for the metal-free, regioselective, remote C-H halogenation of 8-substituted quinolines

Motati, Damoder Reddy,Uredi, Dilipkumar,Watkins, E. Blake

, p. 1782 - 1788 (2018/02/23)

An operationally simple and metal-free p...

Study on Relationship Between Fluorescence Properties and Structure of Substituted 8-Hydroxyquinoline Zinc Complexes

Jianbo, He,Tingting, Zhou,Yongjing, Cao,Yuanyuan, Zhang,Weiqing, Yang,Menglin, Ma

, p. 1121 - 1126 (2018/08/17)

Organic light-emitting diodes (OLEDs) pr...

1198-14-7 Process route

8-quinolinol
148-24-3,24804-14-6

8-quinolinol

5-bromo-8-hydroxyquinoline
1198-14-7

5-bromo-8-hydroxyquinoline

broxyquinoline
521-74-4

broxyquinoline

Conditions
Conditions Yield
With 1,3,5-tribromo-1,3,5-triazinane-2,4,6-trione; In acetonitrile; at 20 ℃; regioselective reaction;
72%
11%
With bromine; acetic acid;
8-quinolinol
148-24-3,24804-14-6

8-quinolinol

5-bromo-8-hydroxyquinoline
1198-14-7

5-bromo-8-hydroxyquinoline

broxyquinoline
521-74-4

broxyquinoline

7-bromo-8-hydroxyquinoline
13019-32-4

7-bromo-8-hydroxyquinoline

Conditions
Conditions Yield
With hydrogen bromide; isopentyl nitrite; In dichloromethane; at 20 ℃; for 16h;
70 % Spectr.
15%
15%

1198-14-7 Upstream products

  • 148-24-3
    148-24-3

    8-quinolinol

  • 13207-66-4
    13207-66-4

    5-amino-8-hydroxyquinoline

  • 40925-68-6
    40925-68-6

    2-amino-4-bromo-phenol

  • 56-81-5
    56-81-5

    glycerol

1198-14-7 Downstream products

  • 37171-61-2
    37171-61-2

    5-bromo-7-iodo-quinolin-8-ol

  • 130-16-5
    130-16-5

    5-Chloro-8-hydroxyquinoline

  • 89-00-9
    89-00-9

    Pyridine-2,3-dicarboxylic acid

  • 1312610-24-4
    1312610-24-4

    C17 H15 NO2

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