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5-(3,4-difluorophenyl)pyridine-3-carboxylic acid is a heterocyclic aromatic carboxylic acid with the molecular formula C12H7F2NO2. It is a derivative of pyridine carboxylic acid, featuring a 3-carboxylic acid group and a 5-(3,4-difluorophenyl) substitution. 5-(3,4-difluorophenyl)pyridine-3-carboxylic acid is potentially useful in medicinal chemistry and drug discovery due to its unique structural properties.

1048486-16-3

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1048486-16-3 Usage

Uses

Used in Pharmaceutical Development:
5-(3,4-difluorophenyl)pyridine-3-carboxylic acid is used as a building block or intermediate in the synthesis of pharmaceuticals for various therapeutic applications. Its heterocyclic structure and functional groups may contribute to the development of new drugs with specific biological activities.
Used in Agrochemicals:
In the agrochemical industry, 5-(3,4-difluorophenyl)pyridine-3-carboxylic acid is used as a key component in the creation of pesticides or herbicides. Its chemical properties may provide selective control over pests or unwanted plant growth, contributing to more effective and targeted agricultural solutions.
Used in Academic Research:
5-(3,4-difluorophenyl)pyridine-3-carboxylic acid serves as a valuable compound in academic research, particularly in the fields of organic chemistry, medicinal chemistry, and materials science. Researchers may explore its reactivity, stability, and potential interactions with biological systems to uncover new insights and applications.
Used in Industrial Product Development:
5-(3,4-difluorophenyl)pyridine-3-carboxylic acid may also find use in the development of various industrial products, such as specialty chemicals, coatings, or materials with unique properties. Its aromatic and heterocyclic nature could contribute to the creation of innovative products with improved performance characteristics.
The specific properties and potential uses of 5-(3,4-difluorophenyl)pyridine-3-carboxylic acid would need to be determined through further experimentation and analysis to fully understand its capabilities and limitations in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1048486-16-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,8,4,8 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1048486-16:
(9*1)+(8*0)+(7*4)+(6*8)+(5*4)+(4*8)+(3*6)+(2*1)+(1*6)=163
163 % 10 = 3
So 1048486-16-3 is a valid CAS Registry Number.

1048486-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3,4-difluorophenyl)pyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:1048486-16-3 SDS

1048486-16-3Downstream Products

1048486-16-3Relevant academic research and scientific papers

Structure-Activity Relationship for the Picolinamide Antibacterials that Selectively Target Clostridioides difficile

Speri, Enrico,Qian, Yuanyuan,Janardhanan, Jeshina,Masitas, Cesar,Lastochkin, Elena,De Benedetti, Stefania,Wang, Man,Schroeder, Valerie A.,Wolter, William R.,Oliver, Allen G.,Fisher, Jed F.,Mobashery, Shahriar,Chang, Mayland

, p. 991 - 995 (2021/05/27)

Clostridioides difficile is a leading health threat. This pathogen initiates intestinal infections during gut microbiota dysbiosis caused by oral administration of antibiotics. C. difficile is difficult to eradicate due to its ability to form spores, which are not susceptible to antibiotics. To address the urgent need for treating recurrent C. difficile infection, antibiotics that selectively target C. difficile over common gut microbiota are needed. We herein describe the class of picolinamide antibacterials which show potent and selective activity against C. difficile. The structure-activity relationship of 108 analogues of isonicotinamide 4, a compound that is equally active against methicillin-resistant Staphylococcus aureus and C. difficile, was investigated. Introduction of the picolinamide core as exemplified by analogue 87 resulted in exquisite potency and selectivity against C. difficile. The ability of the picolinamide class to selectively target C. difficile and to prevent gut dysbiosis holds promise for the treatment of recurrent C. difficile infection.

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