ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyridine compound >Bromopyridine >5-Bromo-2,4-dimethylpyridine

5-Bromo-2,4-dimethylpyridine

5-Bromo-2,4-dimethylpyridine Suppliers list
Company Name: Aikon International Limited  Gold
Tel: 025-58859352 19370895928
Email: sales01@aikonchem.com
Company Name: JinYan Chemicals(ShangHai) Co.,Ltd.  
Tel: 13817811078
Email: sales@jingyan-chemical.com
Company Name: Pure Chemistry Scientific Inc.  
Tel: 001-857-928-2050 or 1-888-588-9418
Email: sales@chemreagents.com
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: Record Tech (Shanghai) Co., LTD  
Tel: 13761627472
Email: 183009664@qq.com

5-Bromo-2,4-dimethylpyridine manufacturers

5-Bromo-2,4-dimethylpyridine Basic information
Product Name:5-Bromo-2,4-dimethylpyridine
Synonyms:PYRIDINE, 5-BROMO-2,4-DIMETHYL-;3-Bromo-4,6-dimethylpyridine;5-BROMO-2,4-DIMETHYLPYRIDINE ISO 9001:2015 REACH;5-Bromo-2,4-dimethylpyridine
CAS:27063-92-9
MF:C7H8BrN
MW:186.05
EINECS:
Product Categories:Heterocycle-Pyridine series
Mol File:27063-92-9.mol
5-Bromo-2,4-dimethylpyridine Structure
5-Bromo-2,4-dimethylpyridine Chemical Properties
Boiling point 205-210 °C
density 1.415±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka4.25±0.18(Predicted)
AppearanceLight yellow to gray Liquid
InChIInChI=1S/C7H8BrN/c1-5-3-6(2)9-4-7(5)8/h3-4H,1-2H3
InChIKeySLMUXUHXAIPROA-UHFFFAOYSA-N
SMILESC1(C)=NC=C(Br)C(C)=C1
Safety Information
HS Code 2933399990
MSDS Information
5-Bromo-2,4-dimethylpyridine Usage And Synthesis
Synthesis
2,5-Dibromo-4-methylpyridine

3430-26-0

Methylmagnesium Bromide

75-16-1

5-BROMO-2,4-DIMETHYLPYRIDINE

27063-92-9

A solution of 2,5-dibromo-4-methylpyridine (2.51 g, 10.0 mmol) in anhydrous THF (50 mL) was added to a three-necked flask, followed by tetrakis(triphenylphosphine)palladium (1.15 g, 1.0 mmol). The reaction mixture was cooled to 0 °C under nitrogen protection and stirred. A THF solution of methylmagnesium bromide (15 mL, 15.0 mmol, 1 mol/L) was added slowly and dropwise. After the dropwise addition, the reaction mixture was heated to reflux for 3 hours. After completion of the reaction, it was cooled to room temperature, the reaction was quenched with 1N hydrochloric acid and extracted with ethyl acetate (100 mL x 3). The organic layers were combined, washed sequentially with water (50 mL x 2) and saturated saline (50 mL) and dried over anhydrous sodium sulfate. After concentration under reduced pressure, the crude product was purified by Biotage fast chromatography (petroleum ether/ethyl acetate = 5%-10%) to afford 2,4-dimethyl-5-bromopyridine (301 mg, 16.2%) as a colorless oil.1H NMR (400 MHz, CDCl3) δppm: 2.35 (d, 3H), 2.47 (s, 3H), 7.04 ( s, 1H), 8.50 (s, 1H).

References[1] Patent: WO2017/221092, 2017, A1. Location in patent: Paragraph 00190
Tag:5-Bromo-2,4-dimethylpyridine(27063-92-9) Related Product Information
3,5-Dibromo-2,4,6-trimethylpyridine 5-Bromo-4-methyl-pyridine-2-carboxylic acid Bis(2,4,6-trimethylpyridine)bromonium hexafluorophosphate 3-Amino-4-methylpyridine 3-Bromo-2,4,6-trimethylpyridine 5-Bromo-2,4-bis(trifluoromethyl)pyridine 5-Bromo-2,4-dimethylpyridine 5-Bromo-4-methyl-pyridine-2-carboxylic acid methyl ester (5-Bromo-4-methyl-pyridin-2-yl)-acetonitrile 2-Amino-3,5-dibromo-4,6-dimethylpyridine 5-Bromo-2-(trifluoromethyl)pyridine-4-carboxylic acid 5-Bromo-4-methyl-pyridine-2-carbonitrile 5-Bromo-4-methyl-pyridine-2-carbaldehyde C-(5-Bromo-4-methyl-pyridin-2-yl)-methylamine (5-Bromo-4-methyl-pyridin-2-yl)-acetic acid methyl ester (5-Bromo-4-methyl-pyridin-2-yl)-acetic acid 2-(5-Bromo-4-methyl-pyridin-2-yl)-ethylamine AKOS 90390