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4-Cyanopyridine N-oxide, 98%|309374|14906-59-3

4-Cyanopyridine N-oxide, 98%

Cat. No JK309374_5_G
J&K Chemical

Product Information

Product Name
4-Cyanopyridine N-oxide, 98%
Brand Name
J&K
Product Number
309374
CAS
14906-59-3
Molecular Formula
C6H4N2O
Molecular Weight
120.11
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
Isonicotinonitrile N-oxide
PubChem CID
84684
IUPAC Name
1-oxidopyridin-1-ium-4-carbonitrile
InChI Key
QNCSFBSIWVBTHE-UHFFFAOYSA-N
SMILES
C1=CN+(=CC=C1C#N)O-

Properties

Melting Point
223-225

Safety Information

Signal Word
Warning
Hazard Statement
H302
H312
H315
H319
H332
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P362+P364
P332+P317
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

2-Difluoromethylpyridine as a bioisosteric replacement of pyridine- N -oxide: the case of quorum sensing inhibitors
Publication Name: RSC Medicinal Chemistry
Publication Date: 2021-12-15
DOI: 10.1039/d1md00245g

Pyridine-Mediated B–B Bond Activation of (RO)2B–B(OR)2 for Generating Borylpyridine Anions and Pyridine-Stabilized Boryl Radicals as Useful Boryl Reagents in Organic Synthesis
Publication Name: Synthesis
Publication Date: 2021-05-25
DOI: 10.1055/a-1486-8169

Boryl Radical Enabled C—C Bond Formation
Publication Name: Science of Synthesis
Publication Date: 2021

Modern Approaches to the Tuning of the Lanthanide(3+) Coordination Compound Luminescent Characteristics: A Review
Publication Name: Theoretical and Experimental Chemistry
Publication Date: 2019-11
DOI: 10.1007/s11237-019-09622-5

Crystal structure of hydrobromides of pyridines and quinolines N-oxides
Publication Name: Russian Journal of General Chemistry
Publication Date: 2017-02
DOI: 10.1134/s1070363217020104

4-Cyanopyridine N-oxide, 98%

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