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7-bromo-5-methylquinolin-8-ol is an organic compound belonging to the quinoline family, characterized by the presence of a bromine atom at the 7th position, a methyl group at the 5th position, and a hydroxyl group at the 8th position. It is known for its potential applications in various fields due to its unique chemical structure and properties.

7175-09-9

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7175-09-9 Usage

Uses

Used in Pharmaceutical Industry:
7-bromo-5-methylquinolin-8-ol is used as an intermediate in the synthesis of various pharmaceutical compounds, particularly those with potential therapeutic applications. Its unique structure allows for the development of new drugs with improved efficacy and reduced side effects.
Used in Chemical Synthesis:
In the field of organic chemistry, 7-bromo-5-methylquinolin-8-ol serves as a key building block for the synthesis of more complex molecules, such as o-chloro hydroxy derivatives in pyridine and quinoline. This makes it a valuable compound for researchers and chemists working on the development of novel chemical entities.
Used in Research and Development:
Due to its unique chemical properties, 7-bromo-5-methylquinolin-8-ol is also used in research and development for the exploration of new chemical reactions and the discovery of new compounds with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 7175-09-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7175-09:
(6*7)+(5*1)+(4*7)+(3*5)+(2*0)+(1*9)=99
99 % 10 = 9
So 7175-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H8BrNO/c1-6-5-8(11)10(13)9-7(6)3-2-4-12-9/h2-5,13H,1H3

7175-09-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-bromo-5-methylquinolin-8-ol

1.2 Other means of identification

Product number -
Other names Tilbroquinolum [INN-Latin]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7175-09-9 SDS

7175-09-9Relevant academic research and scientific papers

Bromine-Lithium Exchange on Bromo-8-hydroxyquinolines via Formation of their Sodium Salts.

Mongin, Florence,Fourquez, Jean-Marie,Rault, Stephanie,Levacher, Vincent,Godard, Alain,et al.

, p. 8415 - 8418 (1995)

A short and versatile method is reported for the preparation of 8-hydroxyquinoline derivatives by reaction of n-butyllithium with 5,7-dibromo-8-hydroxyquinoline 2 and 7-bromo-8-hydroxyquinoline 1 as their sodium salts.Thus, bromine-lithium exchange reaction on compound 2, highly regioselective, gave after addition of various electrophiles, 5-substituted 7-bromo-8-hydroxyquinolines 4a-j in moderate to good yields.The same procedure was also applicable to 7-bromo-8-hydroxyquinoline 1 which led to 7-substituted 8-hydroxyquinolines 3a-b.

Aza-and polyaza-naphthalenly ketones useful as hiv integrase inhibitors

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Page/Page column 43, (2010/02/10)

Certain aza- and polyaza-naphthalenyl ketones including certain quinolinyl and naphthyridinyl ketones are described as inhibitors of HIV integrase and inhibitors of HIV replication. These compounds are useful in the prevention or treatment of infection by HIV and the treatment or the delay in the onset of AIDS, as compounds or pharmaceutically acceptable salts, or as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are also described.

NITROGEN-CONTAINING HETEROARYL COMPOUNDS HAVING HIV INTEGRASE INHIBITORY ACTIVITY

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Page 77; 78, (2008/06/13)

A compound of the formula (I): wherein Z4, Z5 and Z9 each is independently carbon atom or nitrogen atom; Y is hydroxy, mercapto or amino; RA is a group of the formula: (wherein C ring is nitrogen-containing heteroaryl) has an inhibitory activity against integrase.

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