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2-Hydroxy-5-nitropyridine, 99%|285755|5418-51-9

2-Hydroxy-5-nitropyridine, 99%

Cat. No JK285755_100_G
J&K Chemical

Product Information

Product Name
2-Hydroxy-5-nitropyridine, 99%
Brand Name
J&K
Product Number
285755
CAS
5418-51-9
Molecular Formula
C5H4N2O3
Molecular Weight
140.10
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
5-Nitro-2(1H)-pyridone
PubChem CID
79453
IUPAC Name
5-nitro-1H-pyridin-2-one
InChI Key
XKWSQIMYNVLGBO-UHFFFAOYSA-N
SMILES
C1=CC(=O)NC=C1N+(=O)O-

Properties

Melting Point
188-191

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

Synthesis, antimicrobial and thermal studies of nitropyridine-substituted double armed benzo-15-crown-5 ligands; alkali (Na+ and K+) and transition metal (Ag+) complexes; reduction of nitro compounds
Publication Name: Journal of Inclusion Phenomena and Macrocyclic Chemistry
Publication Date: 2022-08-26
DOI: 10.1007/s10847-022-01157-y

C–H Bond Functionalization of Amines: A Graphical Overview of Diverse Methods
Publication Name: SynOpen (2017)
Publication Date: 2021-07
DOI: 10.1055/s-0040-1706051

Pd-catalyzed fluoro-carbonylation of aryl, vinyl, and heteroaryl iodides using 2-(difluoromethoxy)-5-nitropyridine
Publication Name: Communications Chemistry
Publication Date: 2020-05-11
DOI: 10.1038/s42004-020-0304-3

On the Reaction of Malononitrile with Acetylacetone
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2018-10
DOI: 10.1134/s1070428018100214

Synthesis of Amides by Nucleophilic Substitution of Hydrogen in 3-Nitropyridine
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2018-06
DOI: 10.1134/s1070428018060076

2-Hydroxy-5-nitropyridine, 99%

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