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6-Methoxyquinoline-3-carboxamide, a derivative of quinoline with the molecular formula C11H10N2O2, is a chemical compound that features a methoxy group and an amide group. It has garnered attention for its potential biological and pharmacological activities, including anti-cancer, anti-inflammatory, and anti-microbial properties. 6-METHOXYQUINOLINE-3-CARBOXAMIDE's structural and functional attributes position it as a significant entity in medicinal chemistry and drug discovery, with ongoing research into its use in developing novel treatments for a range of medical conditions.

71083-30-2

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71083-30-2 Usage

Uses

Used in Pharmaceutical Industry:
6-Methoxyquinoline-3-carboxamide is utilized as a precursor in the synthesis of various pharmaceuticals due to its unique chemical structure and potential therapeutic effects. Its presence in drug development pipelines underscores its importance in creating new medications for different diseases.
Used in Anti-Cancer Research:
In the field of oncology, 6-Methoxyquinoline-3-carboxamide is employed as a compound with anti-cancer properties. It is being studied for its ability to target and inhibit the growth of cancer cells, making it a candidate for further research into potential cancer treatments.
Used in Anti-Inflammatory Applications:
6-Methoxyquinoline-3-carboxamide is used as an anti-inflammatory agent, leveraging its pharmacological properties to reduce inflammation. This application is crucial in the treatment of various inflammatory conditions and diseases.
Used in Anti-Microbial Research:
6-METHOXYQUINOLINE-3-CARBOXAMIDE is also being investigated for its anti-microbial properties, which could be harnessed in the development of new antibiotics or antifungal agents to combat drug-resistant infections.
Used in Medicinal Chemistry:
6-Methoxyquinoline-3-carboxamide serves as a key compound in medicinal chemistry, where it is used for the exploration of its structure-activity relationships. This helps in optimizing its pharmacological profile for various therapeutic applications.
Overall, 6-Methoxyquinoline-3-carboxamide's multifaceted potential across different medical and pharmaceutical applications highlights its significance in the ongoing quest for innovative treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 71083-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,8 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71083-30:
(7*7)+(6*1)+(5*0)+(4*8)+(3*3)+(2*3)+(1*0)=102
102 % 10 = 2
So 71083-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O2/c1-15-9-2-3-10-7(5-9)4-8(6-13-10)11(12)14/h2-6H,1H3,(H2,12,14)

71083-30-2 Well-known Company Product Price

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  • Aldrich

  • (BBO000247)  6-Methoxyquinoline-3-carboxamide  AldrichCPR

  • 71083-30-2

  • BBO000247-1G

  • 3,540.42CNY

  • Detail

71083-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-METHOXYQUINOLINE-3-CARBOXAMIDE

1.2 Other means of identification

Product number -
Other names 3-Quinolinecarboxamide,6-methoxy

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:71083-30-2 SDS

71083-30-2Relevant academic research and scientific papers

Initial Route Scouting and Final Process Development for the Multi-Kg Production of 3-Fluoro-6-methoxyquinoline from p-Anisidine and 2-Fluoromalonic Acid

Sch?fer, Gabriel,Fleischer, Tony,Blumer, Nicole,Udry, Megan,Reber, Stefan,Stansfield, Ian,Liu, Yuanhua,Li, Yan,Li, Pixu

, p. 347 - 357 (2022/02/01)

A scalable route to 3-fluoro-6-methoxyquinoline needed to be developed as multi-kg amounts of this heterocycle were required. Initial route development focused on the formation of the key C-F bond via a Balz-Schiemann reaction or electrophilic fluorinatio

Synthesis of quinoline derivatives as 5-HT4 receptor ligands

Hanna-Elias, Amir,Manallack, David T.,Berque-Bestel, Isabelle,Irving, Helen R.,Coupar, Ian M.,Iskander, Magdy N.

experimental part, p. 150 - 156 (2009/09/08)

A general and convenient synthesis of 6-methoxyquinoline-3-carboxamides commencing with a cyclization step that involves -anisidine and diethyl (ethoxymethylene)malonate is described. An additional tetrahydroquinoline scaffold 19 is prepared from 6-methox

Novel process for preparing 3-fluoroquinolines

-

Page/Page column 4-5, (2008/06/13)

The invention relates to a novel preparation of 3-fluoroquinolines of formula (I) in which R1, R2, R3 and R4 represent: a) a fluorine; b) an alkyl optionally substituted with one to three fluorines, with OR

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