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5-Fluoro-2-methoxynicotinic acid is a chemical compound with the molecular formula C7H6FNO3, belonging to the nicotinic acid derivatives, which are part of the vitamin B3 complex. 5-Fluoro-2-methoxynicotinic acid features a fluorine atom at the 5-position and a methoxy group at the 2-position on the nicotinic acid ring, endowing it with unique properties and potential for pharmaceutical applications.

884494-82-0

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884494-82-0 Usage

Uses

5-Fluoro-2-methoxynicotinic acid is used as a pharmaceutical intermediate for the development of drugs targeting various diseases and conditions. Its specific applications and reasons are as follows:
Used in Pharmaceutical Industry:
5-Fluoro-2-methoxynicotinic acid serves as a key intermediate in the synthesis of therapeutic agents. Its unique structure, including the fluorine and methoxy substitutions, allows for the creation of new drugs with distinct pharmacological profiles, potentially leading to improved efficacy and selectivity in treating specific medical conditions.
Used in Drug Discovery Research:
In the field of drug discovery, 5-Fluoro-2-methoxynicotinic acid is utilized as a starting point for the design and synthesis of novel compounds. Its chemical properties and interactions with biological targets make it a valuable tool for exploring new therapeutic avenues and understanding the underlying mechanisms of action.
Used in Medicinal Chemistry:
5-Fluoro-2-methoxynicotinic acid is employed in medicinal chemistry for the optimization of drug candidates. Its structural features can be modified to fine-tune the pharmacokinetic and pharmacodynamic properties of new molecules, enhancing their safety, efficacy, and suitability for clinical use.
While the specific applications of 5-Fluoro-2-methoxynicotinic acid in different industries are not explicitly mentioned in the provided materials, its potential uses in the pharmaceutical industry, drug discovery research, and medicinal chemistry are inferred based on its properties and the context of its study. Further research and development are necessary to fully realize its therapeutic potential and explore additional applications across various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 884494-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,4,9 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 884494-82:
(8*8)+(7*8)+(6*4)+(5*4)+(4*9)+(3*4)+(2*8)+(1*2)=230
230 % 10 = 0
So 884494-82-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6FNO3/c1-12-6-5(7(10)11)2-4(8)3-9-6/h2-3H,1H3,(H,10,11)

884494-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Fluoro-2-Methoxynicotinic Acid

1.2 Other means of identification

Product number -
Other names 5-fluoro-2-methoxypyridine-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:884494-82-0 SDS

884494-82-0Relevant articles and documents

PYRIDINONE DERIVATIVES AS SELECTIVE CYTOTOXIC AGENTS AGAINST HIV INFECTED CELLS

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Page/Page column 52, (2020/12/07)

The present disclosure is directed to pyridinone derivatives of Formula I and their use for selectively killing HIV infected GAG-POL expressing cells without concomitant cytotoxicity to HIV nave cells, and for the treatment of infection by HIV, or for the treatment, prophylaxis or delay in the onset or progression of AIDS or AIDS Related Complex (ARC).

MACROCYCLIC COMPOUNDS AS TRK KINASES INHIBITORS

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Paragraph 145; 190; 191, (2019/10/19)

Provided are certain TRK inhibitors, pharmaceutical compositions thereof, and methods of use thereof.

Compounds and methods for kinase modulation, and indications therefor

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Page/Page column 321; 322, (2015/09/22)

Compounds and salts thereof, formulations thereof, conjugates thereof, derivatives thereof, forms thereof and uses thereof are described. In certain aspects and embodiments, the described compounds or salts thereof, formulations thereof, conjugates thereo

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