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6-(3-Chlorophenyl)-picolinic acid is a chemical compound with the molecular formula C12H8ClNO2. It is a derivative of picolinic acid and features a chlorine atom attached to the third position of the phenyl ring. 6-(3-Chlorophenyl)-picolinic acid is characterized by its potential as a ligand in metal coordination complexes and its ability to exhibit bioactivity against certain diseases and pests.

863704-38-5

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863704-38-5 Usage

Uses

Used in Pharmaceutical Research:
6-(3-Chlorophenyl)-picolinic acid is used as a ligand in metal coordination complexes for the development of pharmaceutical agents. Its unique structure allows for the formation of stable complexes with metal ions, which can be utilized in the design of new drugs with improved properties.
Used in Agrochemical Research:
In the agrochemical industry, 6-(3-Chlorophenyl)-picolinic acid is used as a bioactive compound for the development of pesticides and other agrochemicals. Its ability to exhibit bioactivity against certain pests and diseases makes it a promising candidate for the creation of more effective and targeted agrochemical products.
The precise applications and potential effects of 6-(3-Chlorophenyl)-picolinic acid are the subject of ongoing research and development within the scientific community, as its full potential in various fields is yet to be fully explored and understood.

Check Digit Verification of cas no

The CAS Registry Mumber 863704-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,7,0 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 863704-38:
(8*8)+(7*6)+(6*3)+(5*7)+(4*0)+(3*4)+(2*3)+(1*8)=185
185 % 10 = 5
So 863704-38-5 is a valid CAS Registry Number.

863704-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(3-chlorophenyl)pyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-(3-chlorophenyl)-2-pyridinecarboxylic 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:863704-38-5 SDS

863704-38-5Relevant 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.

A chiral picolinic acid ligand, Cl-NAPH-PyCOOH, for CPRU-catalyzed dehydrative allylation: Design, synthesis, and properties

Tanaka, Shinji,Suzuki, Yusuke,Kimura, Takahiro,Kitamura, Masato

, p. 1707 - 1720 (2019/10/01)

A CpRu/Br?nsted acid-combined catalyst, CpRu(II)/pico-linic acid (PyCOOH), acts as an efficient catalyst for the allyl protection/deprotection of alcohols. This discovery has resulted in the development of a new axially chiral ligand, Cl-Naph-PyCOOH (2a;

EP2 RECEPTOR AGONISTS

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Page/Page column 184, (2008/06/13)

A compound of Formula (I) or a salt, solvate and chemically protected form thereof, wherein: R5 is an optionally substituted C5-20 aryl or C4-20 alkyl group; A is selected from the group consisting of Formulae (Ai), (Aii), (Aiii) D is selected from Formulae (Di), (Dii), (Diii), (Div), (Dv) B is selected from the group consisting of Formulae (Bi), (Bii), (Biii), (Biv) (Bv).

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