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4-Nitro-2,6-pyridinedicarboxylic acid, also known as 4-nitropyridine-2,6-dicarboxylic acid, is a chemical compound with the molecular formula C7H3N3O6. It is a nitro-substituted derivative of pyridinedicarboxylic acid, containing two carboxylic acid groups and a nitro group at the 4-position of the pyridine ring. This versatile compound is recognized for its potential in various chemical and material applications.

63897-10-9

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63897-10-9 Usage

Uses

Used in Pharmaceutical Synthesis:
4-Nitro-2,6-pyridinedicarboxylic acid is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Dye Production:
In the dye industry, 4-Nitro-2,6-pyridinedicarboxylic acid is utilized as a precursor in the production of dyes. Its chemical properties enable the creation of a range of colorants used in various applications, including textiles and printing inks.
Used in Agrochemical Development:
4-Nitro-2,6-pyridinedicarboxylic acid is employed as a starting material in the development of agrochemicals. Its reactivity and functional groups make it suitable for the synthesis of compounds that can be used in agriculture to improve crop protection and yield.
Used in Coordination Polymers and Metal-Organic Frameworks:
4-Nitro-2,6-pyridinedicarboxylic acid is used as a ligand in the production of coordination polymers and metal-organic frameworks. Its ability to coordinate with metal ions makes it a valuable component in the creation of materials with potential applications in gas storage, catalysis, and sensor technology.
Used in Organic Optoelectronics:
In the field of organic optoelectronics, 4-Nitro-2,6-pyridinedicarboxylic acid is utilized for the development of materials with specific optical and electronic properties. Its incorporation into devices can enhance performance and contribute to the advancement of technologies such as solar cells and light-emitting diodes.
Used in Chemical Sensing and Catalysis:
4-Nitro-2,6-pyridinedicarboxylic acid is employed in the development of materials for chemical sensing and catalysis. Its chemical reactivity and functional groups make it a promising candidate for the creation of sensors with high sensitivity and selectivity, as well as catalysts for various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 63897-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,9 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63897-10:
(7*6)+(6*3)+(5*8)+(4*9)+(3*7)+(2*1)+(1*0)=159
159 % 10 = 9
So 63897-10-9 is a valid CAS Registry Number.

63897-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitropyridine-2,6-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Nitrodipicolinic 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:63897-10-9 SDS

63897-10-9Relevant academic research and scientific papers

Novel late transition metal catalysts based on iron: Synthesis, structures and ethylene polymerization

Zohuri, Gholam Hossein,Seyedi, Seyed Mohammad,Sandaroos, Reza,Damavandi, Saman,Mohammadi, Ali

scheme or table, p. 160 - 166 (2011/10/03)

In this article we reported synthesis, characterization and ethylene polymerization behavior of two new late transition metal 2,6-bis(imino)pyridine catalysts based on iron(II) possessing different substituents of NO2 (catalyst b) and OMe (catalyst c) at the para position of the pyridine ring. Theoretical study exhibited more positive charge on the central metal of the catalyst b, leading to higher activity offset by lower thermal stability and life time.

Cation Complexing Properties of Synthetic Macrocyclic Polyether-Diester Ligands Containing the Pyridine Subcyclic Unit

Bradshaw, J. S.,Maas, G. E.,Lamb, J. D.,Izatt, R. M.,Christensen J. J.

, p. 467 - 474 (2007/10/02)

Ten new macrocyclic polyether-diester compounds containing a pyridine subcyclic unit substituted in the 4 position with chloro or methoxy groups have been prepared.These compounds along with their unsubstituted pyridine analogues form strong complexes wit

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