Cat. No JK144726_100_G
J&K Chemical

Product Information

Product Name
3-Cyano-6-methyl-2(1H)-pyridinone, 98%
Brand Name
J&K
Product Number
144726
CAS
4241-27-4
Molecular Formula
C7H6N2O
Molecular Weight
134.14
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
  • 3-Cyano-2-hydroxy-6-methylpyridine
  • 3-Cyano-6-methyl-2-pyridone
  • 5-Cyano-6-hydroxy-2-picoline
  • 2-Hydroxy-6-methylnicotinonitrile
PubChem CID
77919
IUPAC Name
6-methyl-2-oxo-1H-pyridine-3-carbonitrile
InChI Key
FIMGYEKEYXUTGD-UHFFFAOYSA-N
SMILES
CC1=CC=C(C(=O)N1)C#N

Properties

Melting Point
293-295

Safety Information

GHS Symbols
Hazard Symbol
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

Effect of a Substituent in the Fourth Position on the Optical Properties of 2-Oxonicotinonitriles

Publication Name: Russian Journal of General Chemistry
Publication Date: 2022-11
DOI: 10.1134/s1070363222110366

Pyridones – Powerful Precursors for the Synthesis of Alkaloids, Their Derivatives, and Alkaloid-Inspired Compounds

Publication Name: Synthesis
Publication Date: 2019-06-18
DOI: 10.1055/s-0037-1611844

Erratum to: One-step multicomponent synthesis of chiral oxazolinyl-zinc complexes

Publication Name: Chemistry Central Journal
Publication Date: 2017-09-20
DOI: 10.1186/s13065-017-0305-1|10.1186/s13065-017-0315-z

Oxyfunctionalization of pyridine derivatives using whole cells of Burkholderia sp. MAK1

Publication Name: Scientific Reports
Publication Date: 2016-12-16
DOI: 10.1038/srep39129

High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors

Publication Name: Antiviral Research
Publication Date: 2011-09
DOI: 10.1016/j.antiviral.2011.06.006

3-Cyano-6-methyl-2(1H)-pyridinone, 98%

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