3,4-Dimethoxy-2-Methylpyridine

3,4-Dimethoxy-2-Methylpyridine Suppliers list
Company Name: Chiba Pharmaceutical Science and technology Co, Ltd.  
Tel: 0531-81313138 13066006660
Email: chibapharm@foxmail.com
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com
Company Name: Henan Anky Chemical Technology Co., Ltd.  
Tel: 17836913271
Email: 3224305243@qq.com
Company Name: Aikon International Limited  
Tel: 025-58859352 19370895928
Email: sales01@aikonchem.com
Company Name: Jinan chemkey pharmaceutical Co., Ltd.  
Tel: 15610156652
Email: baimingshi@163.com

3,4-Dimethoxy-2-Methylpyridine manufacturers

3,4-Dimethoxy-2-Methylpyridine Basic information
Product Name:3,4-Dimethoxy-2-Methylpyridine
Synonyms:3,4-Dimethoxy-2-Methylpyridine;3,4-dimethoxy-2-methylpyridine (pantoprazole impurity);Pantoprazole Impurity 38;Pyridine, 3,4-dimethoxy-2-methyl-
CAS:107512-35-6
MF:C8H11NO2
MW:153.18
EINECS:
Product Categories:
Mol File:Mol File
3,4-Dimethoxy-2-Methylpyridine Structure
3,4-Dimethoxy-2-Methylpyridine Chemical Properties
Boiling point 211.7±35.0 °C(Predicted)
density 1.042±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka7.85±0.10(Predicted)
AppearanceColorless to light yellow Liquid
Safety Information
MSDS Information
3,4-Dimethoxy-2-Methylpyridine Usage And Synthesis
Synthesis
3-HYDROXY-2-METHYL-4(1H)-PYRIDINONE

17184-19-9

Dimethyl sulfate

77-78-1

3,4-Dimethoxy-2-Methylpyridine

107512-35-6

General procedure: 38 g of 3-hydroxy-2-methylpyridin-4(1H)-one was added to a reaction flask and dissolved in a mixed solution of 90 g of water and 35 g of potassium hydroxide with stirring. The reaction temperature was controlled at 10~20°C. 75 g of dimethyl sulfate was slowly added dropwise, and the reaction was held at the same temperature for 20 hours after the dropwise addition. After completion of the reaction, 80 g of dichloromethane was added to the reaction mixture, stirred for 15 minutes and left to stratify. The aqueous layer was extracted once more with 20 g of dichloromethane, stirred for 15 minutes and left to stratify. The two dichloromethane layers were combined and concentrated under reduced pressure. The product was dried under reduced pressure to give 44 g of 3,4-dimethoxy-2-methylpyridine.

References[1] Patent: CN104557692, 2018, B. Location in patent: Paragraph 0030; 0031
Tag:3,4-Dimethoxy-2-Methylpyridine(107512-35-6) Related Product Information
2-Chloromethyl-3,4-dimethoxypyridinium chloride 3,4-Dimethoxy-2-pyridinemethanol 3,4-DIMETHOXY-2-METHYLPYRIDINE HYDROCHLORIDE 2-Pyridinecarbonitrile, 3,4-dimethoxy- 2-Pyridinecarboxaldehyde, 3,4-dimethoxy- 3-Pyridinol,4-methoxy-6-methyl-(6CI,9CI)