59290-34-5

Basic information

• Product Name: 5-Nitropyridine-2-carboxamide
• Synonyms: 5-Nitropicolinamide;5-Nitropyridine-2-carboxamide;5-Nitro-2-carboxaMide;5-nitro-pyridine-2-carboxylic acid aMide
• CAS NO: 59290-34-5
• Molecular Formula: C6H5N3O3
• Molecular Weight: 167.1222
• Mol File: 59290-34-5.mol

Chemical Properties

• Melting Point: 246-247℃
• Boiling Point: 397.8 °C at 760 mmHg
• Flash Point: 194.4 °C
• Appearance: /
• Density: 1.476
• Storage Temp.: Room temperature.
• CAS DataBase Reference: 5-Nitropyridine-2-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Nitropyridine-2-carboxamide(59290-34-5)
• EPA Substance Registry System: 5-Nitropyridine-2-carboxamide(59290-34-5)

Safety Data

• Hazardous Substances Data: 59290-34-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
5-Nitropyridine-2-carboxamide is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and chemical products.
Used in Chemical Industry:
5-Nitropyridine-2-carboxamide serves as a reagent in organic synthesis, facilitating the creation of a range of chemical compounds and contributing to the advancement of chemical research and development.
Used in Research and Development:
5-Nitropyridine-2-carboxamide is used as an intermediate in the production of other chemical compounds, playing a crucial role in the synthesis processes and the creation of novel chemical entities.
Used in Medicinal Applications:
5-Nitropyridine-2-carboxamide is studied for its potential pharmacological properties, including its anti-inflammatory and antioxidant effects, which may contribute to the development of treatments for various diseases and conditions.

Upstream product

• 30651-24-2 5-nitropicolinic acid 
• 4214-76-0 5-nitro-pyridin-2-ylamine 
• 4487-59-6 2-bromo-5-nitropyridine 

Downstream Products

• 100367-55-3 5-nitropyridine-2-carbonitrile 
• 145255-19-2 5-aminopyridine-2-carboxylic acid amide 
• 86873-62-3 5-Acetylaminopyridin-2-carbonsaeure 
• 24242-20-4 5-amino-pyridine-2-carboxylic acid 
• 15069-92-8 5-hydroxypicolinic acid 

Relevant articles and documents

SUBSTITUTED OXOPYRIDINE DERIVATIVES

The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and o edemas, and also ophthalmic disorders.

SUBSTITUTED OXOPYRIDINE DERIVATIVES

The invention relates to substituted oxopyridine derivatives and to processes for preparation thereof, and also to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially of cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

Compositions and methods for the treatment of coccidiosis

Anticoccidial compositions which comprise as active ingredient pyridine derivatives having the formula STR1 wherein R1 is hydrogen atom, a halomethyl group or methyl group; R2 is hydrogen atom or an alkyl group of 1-3 carbon atoms; R3 is hydrogen atom, an alkyl group of 1-3 carbon atoms, allyl group, an alkyl group having 2 or 3 carbon atoms and alkoxy of 1 or 2 carbon atoms as a substituent, an alkyl group having 1-3 carbon atoms and hydroxy as a substituent, an alkanoyl group of 1-18 carbon atoms, a haloacetyl group, an alkenoyl group of 3-11 carbon atoms, an aromatic acyl group, a heterocyclic acyl group, an N-alkylcarbamoyl group of 1-4 carbon atoms in the alkyl moiety or hydroxy group; Provided that when R2 is said alkyl group of 1-3 carbon atoms, R3 is said alkyl group of 1-3 carbon atoms and inorganic acid addition salts thereof.