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3-Pyridinecarbonitrile,5-hydroxy-(9CI)

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Products Intro: Product Name:3-Pyridinecarbonitrile,5-hydroxy-(9cl)
CAS:152803-24-2
Purity:NLT 98% Package:100G;1KG;100KG
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Products Intro: Product Name:152803-24-2 3-Pyridinecarbonitrile,5-hydroxy-(9CI) C6H4N2O
CAS:152803-24-2
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CAS:152803-24-2
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Products Intro: Product Name:3-CYANO-5-HYDROXYPYRIDINE
CAS:152803-24-2
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Products Intro: Product Name:3-Pyridinecarbonitrile,5-hydroxy-(9CI)
CAS:152803-24-2
Purity:98% Package:5KG;1KG

3-Pyridinecarbonitrile,5-hydroxy-(9CI) manufacturers

3-Pyridinecarbonitrile,5-hydroxy-(9CI) Basic information
Product Name:3-Pyridinecarbonitrile,5-hydroxy-(9CI)
Synonyms:5-isocyano-pyridin-3-ol;3-Pyridinecarbonitrile,5-hydroxy-(9CI);5-Hydroxynicotinonitrile;5-Cyano-3-Hydroxypyridine;3-Cyano-5-hydroxypyridine;3-Pyridinecarbonitrile,5-hydroxy;5-Hydroxynicotinonitrile 97%;3-Pyridinecarbonitrile,5-hydroxy-(9cl)
CAS:152803-24-2
MF:C6H4N2O
MW:120.11
EINECS:
Product Categories:PYRIDINE;Heterocyclic Compounds;Heterocycle-Pyridine series
Mol File:152803-24-2.mol
3-Pyridinecarbonitrile,5-hydroxy-(9CI) Structure
3-Pyridinecarbonitrile,5-hydroxy-(9CI) Chemical Properties
Melting point 213-217℃
Boiling point 394.7±27.0 °C(Predicted)
density 1.33±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka7.96±0.10(Predicted)
AppearanceOff-white to light yellow Solid
Water Solubility Slightly soluble in water.
InChIInChI=1S/C6H4N2O/c7-2-5-1-6(9)4-8-3-5/h1,3-4,9H
InChIKeyKAXIYYPIORYZLB-UHFFFAOYSA-N
SMILESC1=NC=C(O)C=C1C#N
CAS DataBase Reference152803-24-2
Safety Information
RIDADR 3439
HazardClass 6.1
PackingGroup 
HS Code 2933399990
MSDS Information
3-Pyridinecarbonitrile,5-hydroxy-(9CI) Usage And Synthesis
Uses3-Cyano-5-hydroxypyridine is active pharmaceutical ingredients.
Synthesis
3-Pyridinecarbonitrile,5-methoxy-(9CI)

298204-74-7

3-Pyridinecarbonitrile,5-hydroxy-(9CI)

152803-24-2

General procedure for the synthesis of 3-cyano-5-hydroxypyridine from 5-methoxynicotinonitrile: 1 g of 5-methoxynicotinonitrile (7.46 mmol) was mixed with 8.62 g of pyridine hydrochloride, and the reaction was heated at 200 °C for 2 hours. After completion of the reaction, the crude product was diluted with water and extracted several times with ether. The aqueous phase was alkalized by addition of sodium bicarbonate and extracted again with ether. The organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 850 mg of 5-hydroxynicotinonitrile as a beige solid in 95% yield. The product was analyzed by LC-MS: m/z 120.94 (M+H+). 1H NMR (400 MHz, DMSO-d6): δ 10.79 (s, 1H, OH), 8.46 (s, 1H, Harom.), 8.42 (s, 1H, Harom.), 7.60 (s, 1H, Harom.).

References[1] Patent: WO2012/101239, 2012, A1. Location in patent: Page/Page column 74
[2] Patent: US2013/85144, 2013, A1. Location in patent: Paragraph 0394; 0395; 0396
[3] Patent: EP2689778, 2014, A1. Location in patent: Paragraph 0238
[4] Patent: WO2014/16433, 2014, A1. Location in patent: Page/Page column 73
[5] Patent: WO2014/16434, 2014, A1. Location in patent: Page/Page column 72
3-Pyridinecarbonitrile,5-hydroxy-(9CI) Preparation Products And Raw materials
Raw materials3-Pyridinecarbonitrile,5-methoxy-(9CI)-->3-CYANOPYRIDINE-5-BORONIC ACID PINACOL ESTER
Tag:3-Pyridinecarbonitrile,5-hydroxy-(9CI)(152803-24-2) Related Product Information
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