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5-Bromo-2-hydroxymethylpyridine

5-Bromo-2-hydroxymethylpyridine Suppliers list
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5-Bromo-2-hydroxymethylpyridine manufacturers

5-Bromo-2-hydroxymethylpyridine Basic information
Product Name:5-Bromo-2-hydroxymethylpyridine
Synonyms:2-HYDROXYMETHYL-5-BROMOPYRIDINE;(5-BROMOPYRID-2-YL)METHANOL;5-BROMO-2-HYDROXYMETHYLPYRIDINE;5-Bromo-2-hydroxymethylpyridin;(5-BROMO-PYRIDIN-2-YL)METHANOL (5-BROMO-2-HYDROXYMETHYLPYRIDINE);(5-Bromopyridin-2-yl)methanol ,98%;5-Bromo-2-pyridinemethanol >;2-Pyridinemethanol, 5-bromo-
CAS:88139-91-7
MF:C6H6BrNO
MW:188.02
EINECS:618-116-0
Product Categories:Pyridine Series;Heterocycle-Pyridine series;blocks;Bromides;Pyridines;Building Blocks;Pyridine
Mol File:88139-91-7.mol
5-Bromo-2-hydroxymethylpyridine Structure
5-Bromo-2-hydroxymethylpyridine Chemical Properties
Melting point 59-60°C
Boiling point 0°C
density 1.668±0.06 g/cm3(Predicted)
Fp 0°C
storage temp. Inert atmosphere,Room Temperature
form powder to crystal
pka13.09±0.10(Predicted)
color White to Light yellow to Light orange
InChIInChI=1S/C6H6BrNO/c7-5-1-2-6(4-9)8-3-5/h1-3,9H,4H2
InChIKeyRUCZFWMEACWFER-UHFFFAOYSA-N
SMILESC1(CO)=NC=C(Br)C=C1
CAS DataBase Reference88139-91-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38-22
Safety Statements 22-26-36/37/39-36
HazardClass IRRITANT
HS Code 2933399990
MSDS Information
5-Bromo-2-hydroxymethylpyridine Usage And Synthesis
Chemical PropertiesLight yellow Cryst
Uses5-Bromo-2-(hydroxymethyl)pyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Synthesis5-bromo-2-pyridinecarboxylic acid, methyl ester (648mg, 3mmol) in 10ml of methanol was slowly added to sodium borohydride (340mg, 9mmol) in an ice bath. After that, the ice bath was removed and the reaction mixture was warmed to room temperature. The reaction was stirred for 12 hours. Then 1N HCl was added to adjust the pH to 1. Afterward, a saturated sodium bicarbonate solution was added to adjust the pH to 8. The mixture was then extracted with ethyl acetate. The organic phase was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. This resulted in the formation of 535mg of white solid, which was identified as 5-bromo-2-pyridinemethanol. The yield of the desired product was 94.8%.
2-Hydroxymethyl-5-bromopyridine
References[1] Journal of Inorganic Biochemistry, 2012, vol. 111, p. 1 - 9
[2] Journal of Porphyrins and Phthalocyanines, 2010, vol. 14, # 6, p. 469 - 480
[3] Patent: US2013/12530, 2013, A1. Location in patent: Paragraph 0178
[4] Patent: WO2008/32191, 2008, A2. Location in patent: Page/Page column 58
[5] Patent: WO2013/13815, 2013, A1. Location in patent: Page/Page column 228
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