25948-12-3

Basic information

• Product Name: 2-[(5-Nitro-2-pyridyl)amino]ethanol
• Synonyms: 2-[(5-Nitro-2-pyridyl)amino]ethan-1-ol;2-[(5-Nitro-2-pyridyl)amino]ethanol;2-[(5-Nitro-2-pyridinyl)amino]ethanol;2-[(5-nitropyridin-2-yl)amino]ethanol hydrochloride;ethanol, 2-[(5-nitro-2-pyridinyl)amino]-
• CAS NO: 25948-12-3
• Molecular Formula: C₇H₉N₃O₃
• Molecular Weight: 183.16
• EINECS: 247-358-6
• Mol File: 25948-12-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 401.9 °C at 760 mmHg
• Flash Point: 196.9 °C
• Appearance: /
• Density: 1.431 g/cm³
• Vapor Pressure: 3.5E-07mmHg at 25°C
• Refractive Index: 1.649
• Storage Temp.: 2-8°C
• PKA: 14.47±0.10(Predicted)
• CAS DataBase Reference: 2-[(5-Nitro-2-pyridyl)amino]ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(5-Nitro-2-pyridyl)amino]ethanol(25948-12-3)
• EPA Substance Registry System: 2-[(5-Nitro-2-pyridyl)amino]ethanol(25948-12-3)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 25948-12-3(Hazardous Substances Data)

Usage

General Description

2-[(5-Nitro-2-pyridyl)amino]ethanol is a chemical compound characterized by the presence of a pyridine ring, a nitro group, an amino group, and an ethanol group in its structure. 2-[(5-Nitro-2-pyridyl)amino]ethanol belongs to the class of organic compounds known as nitropyridines, which are compounds containing a nitro group attached to a pyridine ring. Its systematic name is 2-[(5-Nitropyridin-2-yl)amino]ethan-1-ol. It is used in scientific research due to its ability to bind with other substances and its distinctive properties. However, its exact applications and specific physical and chemical properties, such as boiling point, density, or toxicity, have not been extensively documented. As with any chemical compound, proper handling and safety procedures should be followed while dealing with 2-[(5-Nitro-2-pyridyl)amino]ethanol.

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

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

Downstream Products

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

Relevant articles and documents

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 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.

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.