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3-Bromo-2-hydroxy-5-methylpyridine

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3-Bromo-2-hydroxy-5-methylpyridine manufacturers

3-Bromo-2-hydroxy-5-methylpyridine Basic information
Product Name:3-Bromo-2-hydroxy-5-methylpyridine
Synonyms:3-BROMO-5-METHYL-2(1H)-PYRIDINONE;TIMTEC-BB SBB003679;2-HYDROXY-3-BROMO-5-PICOLINE;3-Bromo-2-hydroxy-5-methylpyridine 98%;3-Bromo-2-hydroxy-5-picoline 17282-02-9;3-BROMO-2-HYDROXY-5-PICOLINE (3-BROMO-2-HYDROXY-5-METHYLPYRIDINE);3-Bromo-5-methyl-2-pyridone;3-Bromo-5-methyl-2-pyridinol
CAS:17282-02-9
MF:C6H6BrNO
MW:188.02
EINECS:623-885-0
Product Categories:blocks;Bromides;Pyridines;Pyridine;Heterocyclic Building Blocks;Halogenated Heterocycles;C6Heterocyclic Building Blocks
Mol File:17282-02-9.mol
3-Bromo-2-hydroxy-5-methylpyridine Structure
3-Bromo-2-hydroxy-5-methylpyridine Chemical Properties
Melting point 78-82 °C (lit.)
Boiling point 324.0±42.0 °C(Predicted)
density 1.622±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka10.95±0.10(Predicted)
form powder to crystal
color White to Orange to Green
BRN 1423374
InChI1S/C6H6BrNO/c1-4-2-5(7)6(9)8-3-4/h2-3H,1H3,(H,8,9)
InChIKeyKHBRMXVUQOVORD-UHFFFAOYSA-N
SMILESCc1cnc(O)c(Br)c1
CAS DataBase Reference17282-02-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-37/38-41-36/37/38
Safety Statements 26-36/37/39-36
RIDADR 1993
WGK Germany 3
Hazard Note Irritant/Keep Cold
PackingGroup III
HS Code 29333990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
3-Bromo-2-hydroxy-5-methylpyridine Usage And Synthesis
Chemical PropertiesWhite solid
Synthesis
2-Hydroxy-5-methylpyridine

1003-68-5

3-BROMO-2-HYDROXY-5-METHYLPYRIDINE

17282-02-9

5-Methylpyridin-2-ol (1 g, 9.16 mmol) was used as starting material and dissolved in 4 mL of carbon disulfide (CS2). Bromine (Br2, 0.47 mL) was slowly added to this solution at room temperature and the reaction mixture was stirred for 2 hours. Upon completion of the reaction, aqueous sodium thiosulfate (Na2S2O3) was added to quench the reaction, followed by extraction of the reaction mixture with ethyl acetate (EtOAc). The organic layer was separated, dried over anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure to afford the solid product 3-bromo-2-hydroxy-5-methylpyridine (1.7 g, 98% yield). The structure of the product was confirmed by 1H-NMR (CDCl3): δ 7.73 (1H, s), 7.22 (1H, s), 2.10 (3H, s).

References[1] Patent: EP3239143, 2017, A2. Location in patent: Paragraph 0168
[2] Patent: US2008/85906, 2008, A1. Location in patent: Page/Page column 15
3-Bromo-2-hydroxy-5-methylpyridine Preparation Products And Raw materials
Raw materials2-Hydroxy-5-methylpyridine-->Carbon disulfide
Tag:3-Bromo-2-hydroxy-5-methylpyridine(17282-02-9) Related Product Information
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