Welcome to LookChem.com Sign In|Join Free
  • or
6-Methoxy-3-quinolinecarboxylic acid, also known as 6-Methyl-3-methoxyquinoline-4-carboxylic acid or 3-Carboxy-6-methoxyquinoline, is a chemical compound belonging to the quinolinecarboxylic acid family. It is a derivative of quinoline and is characterized by its potential biological activity, making it a promising candidate for pharmaceutical and agrochemical synthesis. 6-Methoxy-3quinolinecarboxvlic acid serves as a building block in organic synthesis and is widely utilized as a research tool in medicinal chemistry.

71082-47-8

Post Buying Request

71082-47-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

71082-47-8 Usage

Uses

Used in Pharmaceutical Synthesis:
6-Methoxy-3-quinolinecarboxylic acid is used as an intermediate in the synthesis of various pharmaceuticals for its potential therapeutic applications. Its unique structure allows for the development of new drugs targeting specific diseases.
Used in Agrochemical Synthesis:
In the agrochemical industry, 6-Methoxy-3-quinolinecarboxylic acid is utilized as a key component in the creation of pesticides and other agrochemicals, contributing to enhanced crop protection and yield.
Used in Cancer Treatment Research:
6-Methoxy-3-quinolinecarboxylic acid is being studied for its potential use as an anticancer agent, with research focusing on its ability to target and treat various types of cancer. Its biological activity makes it a valuable compound in the search for novel cancer therapies.
Used in Infectious Disease Treatment Research:
6-Methoxy-3quinolinecarboxvlic acid is also being investigated for its potential applications in the treatment of infectious diseases, given its demonstrated biological activity. The exploration of its properties could lead to the development of new treatments for a range of infectious conditions.
Used as a Building Block in Organic Synthesis:
6-Methoxy-3-quinolinecarboxylic acid serves as a fundamental building block in organic synthesis, enabling the creation of a wide array of chemical compounds with diverse applications across various industries.
Used as a Research Tool in Medicinal Chemistry:
As a research tool in medicinal chemistry, 6-Methoxy-3-quinolinecarboxylic acid aids scientists and researchers in understanding the structure-activity relationships of various biologically active compounds, facilitating the advancement of drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 71082-47-8 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 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71082-47:
(7*7)+(6*1)+(5*0)+(4*8)+(3*2)+(2*4)+(1*7)=108
108 % 10 = 8
So 71082-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO3/c1-15-9-2-3-10-7(5-9)4-8(6-12-10)11(13)14/h2-6H,1H3,(H,13,14)

71082-47-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (BBO000052)  6-Methoxyquinoline-3-carboxylic acid  AldrichCPR

  • 71082-47-8

  • BBO000052-1G

  • 2,575.17CNY

  • Detail

71082-47-8SDS

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-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-methoxy-quinoline-3-carboxylic acid

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:71082-47-8 SDS

71082-47-8Relevant 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

supporting information, 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

Metabotropic glutamate receptor antagonists and their use for treating central nervous system diseases

-

, (2008/06/13)

The present invention provides compounds, and pharmaceutical compositions containing those compounds, that are active at metabotropic glutamate receptors. The compounds are useful for treating neurological diseases and disorders. Methods of preparing the compounds also are disclosed.

Syntheses and Reactions of Diazepinoquinolines

Guendel, Wolf-H.,Bohnert, Sabine

, p. 769 - 777 (2007/10/02)

Three routes for the preparation of diazepinoquinolines (1) have been studied.The best yields resulted by starting from the amides of N-(3-quinolylcarbonyl)-N-alkyl-amino acids (5).Quaternization to 9, intramolecular cyclization under the influence of base to 10, oxidation to 11 and debenzylation by catalytic hydrogenation gave 1. - Keywords: Quinolinium Salts, Cyclization Reaction

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 71082-47-8