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4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLIC ACID is a quinoline-based chemical compound distinguished by the presence of a hydroxyl and a methoxy group on the quinoline ring, along with a carboxylic acid functional group at the 3-position. 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLIC ACID serves as a versatile intermediate in pharmaceutical synthesis and a valuable building block in the development of novel chemical entities with biological activity.

28027-16-9

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28027-16-9 Usage

Uses

Used in Pharmaceutical Industry:
4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLIC ACID is used as a pharmaceutical intermediate for the synthesis of various drugs, including antimalarial and antibacterial agents. Its unique structure allows for the development of new therapeutic agents with potential applications in treating a range of diseases.
Used in Research and Development:
In the field of research and development, 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLIC ACID is utilized as a building block for the creation of new chemical compounds with biological activity. Its structural features enable the design and synthesis of innovative molecules with potential applications in medicine, agriculture, and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 28027-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,2 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28027-16:
(7*2)+(6*8)+(5*0)+(4*2)+(3*7)+(2*1)+(1*6)=99
99 % 10 = 9
So 28027-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO4/c1-16-6-2-3-9-7(4-6)10(13)8(5-12-9)11(14)15/h2-5H,1H3,(H,12,13)(H,14,15)

28027-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxy-4-oxo-1H-quinoline-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-6-methoxy-chinolin-3-carbonsaeure

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:28027-16-9 SDS

28027-16-9Relevant academic research and scientific papers

Synthesis of novel 3,4,6-trisubstituted quinolines enabled by a Gould-Jacobs cyclization

Trah, Stephan,Lamberth, Clemens

, p. 794 - 796 (2017/03/31)

A Gould-Jacobs cyclization enabled the synthesis of several novel, so far undescribed 3,4,6-trisubstituted quinoline derivatives. They all bear substituents which are well-suited for further transformations, e.g. carboxylic acid or ester functions, haloge

Preparation of quinoline hexose analogs as novel chloroquine-resistant malaria treatments (1). Synthesis of 4-hydroxyquinoline-β-glucosides

Suzuki, Hiroshi,Aly, Nagwa S. M.,Wataya, Yusuke,Kim, Hye-Sook,Tamai, Ikumi,Kita, Masaki,Uemura, Daisuke

, p. 821 - 824 (2008/02/13)

Quinoline hexose analogs are expected to be useful as novel agents for treatment of chloroquine-resistant malaria. Here, we report preparation of 4-hydroxy quinoline-β-glucosides from anilines in 4 steps.

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