25948-12-3

Usage

Uses

Used in Scientific Research:
2-[(5-Nitro-2-pyridyl)amino]ethanol is used as a research chemical for its ability to bind with other substances and its distinctive properties. This makes it valuable in various scientific studies and experiments.
Used in Chemical Synthesis:
In the field of organic chemistry, 2-[(5-Nitro-2-pyridyl)amino]ethanol is used as an intermediate or a building block in the synthesis of more complex molecules, contributing to the development of new compounds with potential applications in various industries.
Used in Pharmaceutical Development:
Although not extensively documented, 2-[(5-Nitro-2-pyridyl)amino]ethanol may have potential applications in the pharmaceutical industry. Its unique structure and properties could be harnessed in the design and synthesis of new drugs, particularly in areas where its binding capabilities could be exploited for therapeutic purposes.
Used in Material Science:
The distinctive properties of 2-[(5-Nitro-2-pyridyl)amino]ethanol may also find applications in material science, where its interaction with other substances could be utilized to develop new materials with specific properties, such as improved conductivity, stability, or reactivity.

InChI:InChI=1/C7H9N3O3/c11-4-3-8-7-2-1-6(5-9-7)10(12)13/h1-2,5,11H,3-4H2,(H,8,9)

Upstream product

• 4548-45-2 2-chloro-5-nitropyridine 
• 141-43-5 ethanolamine 
• 5418-51-9 5-nitro-2-hydroxypyridine 

Downstream Products

• 1419603-50-1 phenyl 6-(2-hydroxyethylamino)pyridin-3-ylcarbamate 
• 1419599-01-1 1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-hydroxyethylamino)pyridin-3-yl)urea 
• 1419599-04-4 1-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-hydroxyethylamino)pyridin-3-yl)urea 
• 1419599-31-7 1-((1-(3,4-difluorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-3-(6-(2-hydroxyethylamino)pyridin-3-yl)urea 

Relevant academic research and scientific papers

SUBSTITUTED HETEROCYCLIC AZA DERIVATIVES

The invention relates to heterocyclic aza derivatives as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

SUBSTITUTED HETEROAROMATIC PYRAZOLE-CONTAINING CARBOXAMIDE AND UREA DERIVATIVES AS VANILLOID RECEPTOR LIGANDS

The invention relates to substituted heteroaromatic pyrazole-containing carboxamide and urea derivatives as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

Substituted Heterocyclic Aza Compounds

Heterocyclic aza compounds as vanilloid receptor ligands, pharmaceutical compositions containing these compounds and also methods of using these compounds for the treatment and/or inhibition of pain and further diseases and/or disorders.

Substituted Heteroaromatic Pyrazole-Containing Carboxamide and Urea Compounds as Vanilloid Receptor Ligands

Substituted heteroaromatic pyrazole-containing carboxamide and urea compounds as vanilloid receptor ligands, pharmaceutical compositions containing these compounds and also to a method of using these compounds for treating and/or inhibiting pain and further diseases and/or disorders.

Process for the production of 2,5-diamino-6-nitro-pyridine derivatives, their use in hair dye compositions and new 2,5-diamino-6-nitropyridine derivatives

A process for producing 2,5-diamino-6-nitropyridine derivatives having the general formula (I) STR1 wherein R1 to R4 represent hydrogen or the radicals alkyl, hydroxy alkyl, dihydroxy alkyl, alkoxy alkyl, alkoxy carbonyl, hydroxy- or chlorine-substituted alkoxy carbonyl, aminoalkyl and aminoalkyl substituted by alkyl or hydroxy alkyl groups, the alkyl groups in each case containing 1 to 4 carbon atoms or an oxazolidinone ring being formed by R1 and R2 and/or R3 and R4. The present invention also relates to novel 2,5-diamino-6-nitropyridine derivatives and to a hair dyeing agent containing 2,5-diamino-6-nitropyridine derivatives, which are direct nitro dyes coloring the hair yellow orange to blue violet and are physiologically harmless.

Chemotherapeutically effective nitro compounds. III. Nitropyridines, nitroimidazopyridines and related compounds

New 2 nitropyridines and 3 nitropyridines, and 3 nitroimidazo [1,2 a] pyridines and related compounds (together 106) were synthesized and tested for their chemotherapeutic efficacy against trichomonads, amoebas and other organisms, such as Eimeria tenella, bacteria, fungi and helminths. Several 2 nitropyridines revealed a detectable systemic effect against Entamoeba histolytica (extraintestinal amoebiasis of the golden hamster) and also a weak activity against Trichomonas fetus in the NMRI mouse. Only a few 3 nitropyridines showed a marked systemic effect against trichomonads. Of the 3 nitroimidazo [1,2 a] pyridines, only the electroneutral carboxylic acid amide group exhibited a pronounced activity, exclusively against trichomonads; however, the activity was nullified by electronegative, electropositive and other electroneutral substituents. As they were not superior in chemotherapeutic respect compared to the known standard preparations (metronidazole), no further tests were carried out with the most effective compounds.