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3-ACETYL-5-BROMOPYRIDINE

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CAS:38940-62-4
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3-ACETYL-5-BROMOPYRIDINE manufacturers

  • 3-ACETYL-5-BROMOPYRIDINE
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  • $15.00 / 1KG
  • 2021-07-02
  • CAS:38940-62-4
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
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  • 3-ACETYL-5-BROMOPYRIDINE
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  • $9.80 / 1.79999995231628KG
  • 2020-01-13
  • CAS:38940-62-4
  • Min. Order: 1g
  • Purity: ≥99%
  • Supply Ability: 100kg
3-ACETYL-5-BROMOPYRIDINE Basic information
Product Name:3-ACETYL-5-BROMOPYRIDINE
Synonyms:3-ACETYL-5-BROMOPYRIDINE;1-(5-BROMOPYRIDIN-3-YL)ETHANONE;Ethanone, 1-(5-bromo-3-pyridinyl)-;3-BROMO-5-ACETYLPYRIDINE;5-Acetyl-3-bromopyridine;1-(5-broMopyridin-3-yl)ethan-1-one;3-Acetyl-5-bromopyridine,97%;5-Bromo-3-acetylpyridine
CAS:38940-62-4
MF:C7H6BrNO
MW:200.03
EINECS:623-602-0
Product Categories:Heterocycle-Pyridine series;API intermediates;Pyridines
Mol File:38940-62-4.mol
3-ACETYL-5-BROMOPYRIDINE Structure
3-ACETYL-5-BROMOPYRIDINE Chemical Properties
Melting point 77-79°C
Boiling point 279.3±25.0 °C(Predicted)
density 1.534±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
solubility soluble in Methanol
pka1.08±0.20(Predicted)
form powder to crystal
color White to Light yellow
BRN 112808
InChIKeyLDBPZEQZCOUYFT-UHFFFAOYSA-N
CAS DataBase Reference38940-62-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 36/37/38-22
Safety Statements 26-36/37/39-36/37-36
WGK Germany 3
HS Code 29333990
MSDS Information
ProviderLanguage
ALFA English
3-ACETYL-5-BROMOPYRIDINE Usage And Synthesis
Chemical PropertiesHoar or pale yellow solid
Uses3-Acetyl-5-bromopyridine is used in the synthesis of benzimidazole CYP11B2 inhibitors. Potent and selective aldosterone inhibitors are used to treat diseases such as those resulting in the stiffening of the heart.
Synthesis
Methylmagnesium Bromide

75-16-1

5-BROMO-N-METHOXY-N-METHYLNICOTINAMIDE

183608-47-1

3-ACETYL-5-BROMOPYRIDINE

38940-62-4

To a solution of 5-bromo-N-methoxy-N-methylnicotinamide (2.08 g, 8.5 mmol) in tetrahydrofuran (THF, 20 mL) was slowly added methylmagnesium bromide (MeMgBr, 1.52 g, 12.75 mmol) at -78 °C. The reaction mixture was stirred at room temperature for 2 h before the reaction was quenched with deionized water. Subsequently, the reaction mixture was extracted with ethyl acetate (EtOAc) and the organic layer was washed with saturated brine and dried over anhydrous sodium sulfate (Na2SO4). After filtration, the filtrate was concentrated under reduced pressure and the resulting residue was purified by fast column chromatography to afford the target product 3-acetyl-5-bromopyridine (1.5 g, 88% yield).

References[1] Patent: US2013/72679, 2013, A1. Location in patent: Paragraph 0893; 0894
[2] Patent: WO2013/37779, 2013, A1. Location in patent: Page/Page column 235; 236
Tag:3-ACETYL-5-BROMOPYRIDINE(38940-62-4) Related Product Information
3-ACETYL-5-BROMOPYRIDINE 3-ACETYL-2-BROMOPYRIDINE 2-METHYLPROPYLHYDRAZINE HYDROCHLORIDE 2-Bromo-6-(2-methyl-1,3-dioxolan-2-yl)pyridine 2-Acetyl-5-bromopyridine 5-Acetyl-2-bromopyridine 2-Acetyl-6-bromopyridine,2-ACETYL-6-BROMOPYRIDINE 97 5-Bromopyridine-3-beta-oxo-propanoic acid ethyl ester 3-(3-ACETOXYBENZOYL)-5-BROMOPYRIDINE 3-(2-ACETOXYBENZOYL)-5-BROMOPYRIDINE 3-BROMO-5-(2-ETHOXYCARBONYLBENZOYL)PYRIDINE 3-(4-ACETOXYBENZOYL)-5-BROMOPYRIDINE 1-(5-BROMOPYRIDIN-3-YL)-2-(METHYLSULFONYL)ETHANONE 3-(5-BROMO-PYRIDIN-3-YL)-3-OXO-PROPIONITRILE 4-ACETYL-2-BROMOPYRIDINE HYDROBROMIDE 2-ACETYL-6-BROMOPYRIDINE 3-BROMO-5-(4-CHLORO-3-FLUOROBENZOYL)PYRIDINE 3-BROMO-5-(4-N-PROPYLBENZOYL)PYRIDINE

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