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Quinoline, 6,8-dimethoxy-, also known as 6,8-dimethoxyquinoline, is a heterocyclic aromatic compound with the molecular formula C11H11NO2. It features a quinoline ring with two methoxy substituents at the 6 and 8 positions. Quinoline, 6,8-dimethoxyis commonly used in the synthesis of pharmaceuticals and natural products, as well as in research for its potential biological activities. Its properties and uses make it a valuable compound in various fields, including medicinal chemistry, chemical biology, and drug discovery.

111454-91-2

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111454-91-2 Usage

Uses

Used in Pharmaceutical Synthesis:
Quinoline, 6,8-dimethoxyis used as a key intermediate in the synthesis of various pharmaceuticals and natural products. Its unique structure and functional groups make it a versatile building block for the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry Research:
Quinoline, 6,8-dimethoxyis employed as a research compound in medicinal chemistry to explore its potential biological activities and therapeutic applications. Its heterocyclic structure and methoxy substituents contribute to its diverse chemical and biological properties, making it a promising candidate for drug discovery and development.
Used in Antimicrobial Applications:
Quinoline, 6,8-dimethoxyhas been investigated for its potential antimicrobial properties. Its ability to inhibit the growth of various microorganisms, including bacteria and fungi, makes it a subject of interest for the development of new antimicrobial agents to combat drug-resistant infections.
Used in Anticancer Applications:
Quinoline, 6,8-dimethoxyhas also been studied for its potential anticancer properties. Its ability to target and inhibit the growth of cancer cells, as well as its potential to enhance the efficacy of existing chemotherapeutic drugs, makes it a promising candidate for further research and development in cancer therapy.
Used in Anti-inflammatory Applications:
Quinoline, 6,8-dimethoxyhas been explored for its potential anti-inflammatory properties. Its ability to modulate inflammatory pathways and reduce inflammation in various disease models makes it a valuable compound for the development of new anti-inflammatory drugs to treat conditions such as arthritis, asthma, and inflammatory bowel disease.

Check Digit Verification of cas no

The CAS Registry Mumber 111454-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,5 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111454-91:
(8*1)+(7*1)+(6*1)+(5*4)+(4*5)+(3*4)+(2*9)+(1*1)=92
92 % 10 = 2
So 111454-91-2 is a valid CAS Registry Number.

111454-91-2SDS

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 6,8-Dimethoxyquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,6,8-dimethoxy

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:111454-91-2 SDS

111454-91-2Relevant academic research and scientific papers

Sequential alkylation/gold-catalyzed annulation reactions of anilines with propargylic bromide derivatives

Alfonsi, Maria,Arcadi, Antonio,Chiarini, Marco,Marinelli, Fabio

experimental part, p. 5145 - 5148 (2011/10/19)

Preliminary results of sequential alkylation/gold-catalyzed annulation reactions of anilines with propargylic bromide derivatives to provide quinoline scaffolds are described. The efficiency of NaAuCl4·2H 2O in the sequential procedu

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