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3,3'-Bipyridine-5-carboxylic acid, also known as bipyridine carboxylic acid, is an organic compound with the chemical formula C11H8N2O2. It is a derivative of bipyridine, featuring a carboxylic acid functional group at the 5-position. 3,3'-Bipyridine-5-carboxylic acid is known for its ability to form stable complexes with transition metals, making it a versatile building block in coordination chemistry and material science.

1970-81-6

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1970-81-6 Usage

Uses

Used in Coordination Chemistry:
3,3'-Bipyridine-5-carboxylic acid is used as a ligand for the synthesis of transition metal complexes. Its ability to chelate metal ions through its nitrogen atoms and the carboxylic acid group enhances the stability and properties of the resulting complexes. This application is particularly relevant in the fields of catalysis, where metal complexes can act as catalysts for various chemical reactions.
Used in Material Science:
In material science, 3,3'-Bipyridine-5-carboxylic acid is used as a building block for the development of new materials with unique properties. The metal complexes formed with this ligand can exhibit interesting electronic, magnetic, and optical characteristics, making them suitable for applications in sensors, electronic devices, and photovoltaic cells.
Used in Pharmaceutical Industry:
3,3'-Bipyridine-5-carboxylic acid and its metal complexes can also be explored for their potential pharmaceutical applications. The ability of this ligand to form stable complexes with metal ions can be exploited to develop new drugs with improved bioavailability, targeting, and reduced side effects.
Used in Environmental Applications:
The chelating properties of 3,3'-Bipyridine-5-carboxylic acid can be utilized in environmental applications, such as the removal of heavy metal ions from contaminated water or soil. The formation of stable metal complexes can help in the sequestration and safe disposal of toxic metal ions, thus mitigating their harmful effects on the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 1970-81-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1970-81:
(6*1)+(5*9)+(4*7)+(3*0)+(2*8)+(1*1)=96
96 % 10 = 6
So 1970-81-6 is a valid CAS Registry Number.

1970-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-pyridin-3-ylpyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3,3'-Bipyridin-5-carbonsaeure

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:1970-81-6 SDS

1970-81-6Downstream Products

1970-81-6Relevant academic research and scientific papers

NEW COMPOUNDS AND METHODS

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Page/Page column 63, (2021/03/19)

The present invention relates to compounds of Formula (I) or a pharmaceutically acceptable salt, solvate, hydrate, tautomer, optical isomer, N-oxide, and/or prodrug thereof. The present invention also relates to pharmaceutical compositions comprising the compounds of the invention, and to their use in the treatment or prevention of medical conditions in which inhibition of c-Abl is beneficial. (I)

POLYVIOLOGEN BORONIC ACID QUENCHERS FOR USE IN ANALYTE SENSORS

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Paragraph 0047, (2015/07/02)

The invention relates to a class of glucose-responsive, polyviologen boronic acid quenchers that may be used in combination with fluophores to achieve real-time measurement of glucose levels in vivo.

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