190616
2-Hydroxy-3-nitropyridine
98%
Synonym(s):
3-Nitro-2-pyridinol, 3-Nitro-2-pyridone
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About This Item
Assay
98%
mp
212 °C (dec.) (lit.)
SMILES string
Oc1ncccc1[N+]([O-])=O
InChI
1S/C5H4N2O3/c8-5-4(7(9)10)2-1-3-6-5/h1-3H,(H,6,8)
InChI key
BOAFCICMVMFLIT-UHFFFAOYSA-N
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General description
2-Hydroxy-3-nitropyridine reacts with phosphorus pentachloride and phosphoryl chloride to yield 2-chloro-3-nitropyridine.
Application
2-Hydroxy-3-nitropyridine was used in the synthesis of:
- 3-nitro-2-pyridyl β-D-galactoside
- 3-nitro-2-pyridyl N-acetyl-β-D-glucosaminide
- 5-amino-6-chloro-3-iodopyridine
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Bioorganic & medicinal chemistry letters, 13(3), 525-527 (2003-02-05)
Racemic 5-azidoepibatidine [(+/-)-1] was synthesized via 5-aminoepibatidine as a candidate photoaffinity ligand with exceptionally high affinity at the mammalian neuronal nicotinic receptors (K(i) values of 0.027 nM for alpha 4 beta 2 and 9.7 nM for alpha 7) and excellent
Nitropyridyl glycosides: new glycosyl donors for enzymatic transglycosylation.
Tetrahedron Letters, 40(36), 6585-6589 (1999)
85. Nucleophilic displacement reactions in aromatic systems. Part I. Kinetics of the reactions of chloronitropyridines with aromatic amines and with pyridine.
Journal of the Chemical Society, 437-446 (1952)
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