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2-Hydroxy-5-methylpyridine

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CAS:1003-68-5
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CAS:1003-68-5
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CAS:1003-68-5
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2-Hydroxy-5-methylpyridine Basic information
Product Name:2-Hydroxy-5-methylpyridine
Synonyms:6-HYDROXY-3-PICOLINE;5-METHYL-2(1H)PYPRIDINONE;5-METHYL-2(1H)-PYRIDINONE;5-METHYL-2(1H)PYRIDONE;5-METHYL-2-PYRIDINOL;5-METHYL-PYRIDIN-2-OL;5-METHYLPYRIDINE-2-ONE;AKOS BBS-00002970
CAS:1003-68-5
MF:C6H7NO
MW:109.13
EINECS:213-713-9
Product Categories:Imidazoles;Heterocycle-Pyridine series;alcohol;Pyridine;Pyridines;Chemical Amines;Amines;Aromatics;Heterocycles;C6;Heterocyclic Building Blocks
Mol File:1003-68-5.mol
2-Hydroxy-5-methylpyridine Structure
2-Hydroxy-5-methylpyridine Chemical Properties
Melting point 183-187 °C (lit.)
Boiling point 304.2±15.0 °C(Predicted)
density 1.053±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)
form Solid
pka12.43±0.10(Predicted)
color Pale Yellow to Light Yellow
BRN 107074
InChIInChI=1S/C6H7NO/c1-5-2-3-6(8)7-4-5/h2-4H,1H3,(H,7,8)
InChIKeySOHMZGMHXUQHGE-UHFFFAOYSA-N
SMILESC1(=O)NC=C(C)C=C1
CAS DataBase Reference1003-68-5(CAS DataBase Reference)
NIST Chemistry Reference2(1H)-pyridinone, 5-methyl-(1003-68-5)
Safety Information
Hazard Codes Xn
Risk Statements 22-37/38-41-36/37/39
Safety Statements 26-36-37
WGK Germany 3
HS Code 29333990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
2-Hydroxy-5-methylpyridine Usage And Synthesis
Chemical PropertiesWhite Solid
Uses2-Hydroxy-5-methylpyridine (cas# 1003-68-5) is a useful compound for organic synthesis. In particular it has been used for the diastereoselective preparation of cyclobutane-fused pyridinyl sulfonyl fluorides.
DefinitionChEBI: 5-Methyl-2-pyridinol is a member of methylpyridines.
Synthesis 3-cyano-6-hydroxypyridine and sodium lauryl sulfate were added to a mixed solvent of n-butanol and water. Subsequently, the temperature was raised to 50 °C., and sulfuric acid water obtained by dissolving 98% sulfuric acid in water was added dropwise at the temperature. After stirring for about 20 minutes, the mixture was cooled to room temperature, and 5% Pd / C was added. The system was replaced with hydrogen, and hydrogenation was carried out at atmospheric pressure for 6 hours. After the reaction was completed, the catalyst was removed by filtration, and the solution was washed with 10% sodium hydroxide aqueous solution. After partially neutralizing to H = 5 and extraction with n-butanol, a solution of crude 3-methyl-6-hydroxypyridine in butanol was obtained. When this solution was quantified by liquid chromatography, the pass-through rate was 99.2%, and the yield of 2-hydroxy-5-methylpyridine was 83%.
Tag:2-Hydroxy-5-methylpyridine(1003-68-5) Related Product Information
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