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6-methoxy-4-methyl-8-nitro-quinoline is a quinoline derivative with the molecular formula C11H10N2O3, featuring a methoxy and nitro group attached to its structure. This chemical compound has garnered interest for its potential pharmaceutical properties, such as antibacterial, antifungal activities, and its exploration in cancer therapy. Its unique structure and properties position it as a promising candidate for further research and development in medicinal chemistry, particularly for the creation of new drug scaffolds.

64992-56-9

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64992-56-9 Usage

Uses

Used in Pharmaceutical Industry:
6-methoxy-4-methyl-8-nitro-quinoline is used as a potential active pharmaceutical ingredient for its demonstrated antibacterial and antifungal activities, offering a new avenue for the development of treatments against resistant infections.
Used in Cancer Therapy Research:
In the field of oncology, 6-methoxy-4-methyl-8-nitro-quinoline is being investigated for its potential as an anticancer agent, with the aim of identifying its mechanisms of action and evaluating its efficacy against various types of cancer.
Used in Medicinal Chemistry for Drug Scaffold Development:
6-methoxy-4-methyl-8-nitro-quinoline serves as a chemical scaffold in the design and synthesis of new drugs, leveraging its unique structure to create novel compounds with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 64992-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,9 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64992-56:
(7*6)+(6*4)+(5*9)+(4*9)+(3*2)+(2*5)+(1*6)=169
169 % 10 = 9
So 64992-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O3/c1-7-3-4-12-11-9(7)5-8(16-2)6-10(11)13(14)15/h3-6H,1-2H3

64992-56-9SDS

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-methyl-8-nitroquinoline

1.2 Other means of identification

Product number -
Other names 6-Methoxy-4-methyl-8-nitro-chinolin

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:64992-56-9 SDS

64992-56-9Relevant academic research and scientific papers

Syntheses, neural protective activities, and inhibition of glycogen synthase kinase-3β of substituted quinolines

Lu, Jianyu,Maezawa, Izumi,Weerasekara, Sahani,Erenler, Ramazan,Nguyen, Tuyen D.T.,Nguyen, James,Swisher, Luxi Z.,Li, Jun,Jin, Lee-Way,Ranjan, Alok,Srivastava, Sanjay K.,Hua, Duy H.

supporting information, p. 3392 - 3397 (2014/07/22)

A new series of fifteen 5-, 6-, and 8-appended 4-methylquinolines were synthesized and evaluated for their neural protective activities. Selected compounds were further examined for their inhibition of glycogen synthase kinase-3β (GSK-3β) and protein kina

Synthesis of amino acid derivatives of 8--6-methoxy-4-substituted/4,5-disubstituted-quinolines as potential antimalarial agents

Jain, Rahul,Jain, Sanjay,Gupta, R C,Anand, Nitya,Dutta, G P,Puri, S K

, p. 251 - 254 (2007/10/02)

Amino acid derivatives 5a-l of 4-substituted/4,5-disubstituted 6-methoxy-8-quinolines (3a-d) have been synthesised and evaluated for radical curative antimalarial activity against P. cynomolgi in rhesus monkeys, and subacute

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