ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyridine compound >Hydroxypyridine >3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE

3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE

3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE Suppliers list
Company Name: Jinan Carbotang Biotech Co.,Ltd.
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Products Intro: Product Name:3-bromo-5-chloropyridin-2-ol
CAS:137628-16-1
Purity:98% Package:5KG;1KG
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Products Intro: Product Name:3-Bromo-5-chloro-2-hydroxypyridine
CAS:137628-16-1
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-17763
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Products Intro: Product Name:3-Bromo-5-chloropyridin-2-ol
CAS:137628-16-1
Purity:0.98 Package:1g;5g;25g;3059g
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Products Intro: Product Name:3-bromo-5-chloro-2-hydroxypyridine
CAS:137628-16-1
Purity:99% Package:1kg
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Products Intro: Product Name:3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE
CAS:137628-16-1
Purity:98% Package:1KG;3USD

3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE manufacturers

3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE Basic information
Product Name:3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE
Synonyms:3-BROMO-5-CHLORO-2-HYDROXYPRIDINE;2-HYDROXY-3-BROMO-5-CHLOROPYRIDINE;3-BROMO-5-CHLOROPYRIDIN-2-OL;3-bromo-5-chloropyridin-2(1H)-one;3-Bromo-5-chloro-2(1H)-pyridinone;3-Bromo-5-chloro-2-pyridone;3-Bromo-5-chloropyridin-2-one;3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE
CAS:137628-16-1
MF:C5H3BrClNO
MW:208.44
EINECS:
Product Categories:Pyridine Series;Pyridine;Halides;Pyridines
Mol File:137628-16-1.mol
3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE Structure
3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE Chemical Properties
Boiling point 277.6±40.0 °C(Predicted)
density 1.91±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka8.48±0.10(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2933399990
MSDS Information
3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE Usage And Synthesis
Synthesis
5-CHLORO-2-HYDROXYPYRIDINE

4214-79-3

3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE

137628-16-1

General procedure for the synthesis of 2-hydroxy-5-chloro-3-bromopyridine from 5-chloropyridin-2-one: 5-chloro-2-hydroxypyridine (20.1 g, 155.4 mmol) and bromine (11.9 mL) were dissolved in acetic acid (250 mL), and the reaction was stirred for 2 hours at room temperature. Upon completion of the reaction, the solvent was removed by vacuum evaporation. The residue was extracted by adding ethyl acetate (600 mL) and saturated sodium bicarbonate solution (300 mL). The organic layer was washed sequentially with saturated sodium bicarbonate solution (2 x 200 mL) and brine, followed by drying and concentration with anhydrous sodium sulfate to give the crude product. The crude product was recrystallized by hexane/ether mixed solvent to afford purified 3-bromo-5-chloro-2-hydroxypyridine (21.3 g, 66% yield), which could be used directly in the subsequent reaction.

References[1] Patent: WO2004/72037, 2004, A1. Location in patent: Page 11
[2] Bioorganic and Medicinal Chemistry Letters, 1998, vol. 8, # 19, p. 2777 - 2782
[3] Patent: US5861419, 1999, A
[4] Patent: US6245797, 2001, B1
[5] Patent: WO2014/141110, 2014, A2. Location in patent: Page/Page column 83; 84
3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE Preparation Products And Raw materials
Raw materials5-CHLORO-2-HYDROXYPYRIDINE-->Ethyl acetate-->Acetic acid-->Sodium bicarbonate
Tag:3-BROMO-5-CHLORO-2-HYDROXYPYRIDINE(137628-16-1) Related Product Information
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