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4-Chloro-2,3-dimethylpyridine 1-oxide

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Products Intro: Product Name:4-Chloro-2,3-dimethylpyridine 1-oxide
CAS:59886-90-7
Purity:0.97 Package:1 g 2 g, 5 g, 10 g, 1000 g
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Products Intro: Product Name:2,3-Dimethyl-4-chloropyridine N-oxide
CAS:59886-90-7
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:59886-90-7 4-Chloro-2,3-dimethylpyridine 1-oxide
CAS:59886-90-7
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CAS:59886-90-7
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Products Intro: Product Name:4-Chloro-2,3-dimethylpyridine 1-oxide
CAS:59886-90-7
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4-Chloro-2,3-dimethylpyridine 1-oxide manufacturers

4-Chloro-2,3-dimethylpyridine 1-oxide Basic information
Product Name:4-Chloro-2,3-dimethylpyridine 1-oxide
Synonyms:4-Chloro-2,3-dimethylpyridine-N-oxide ,98%;4-Chloro-2,3-dimethy;3-DiMethyl-4-chloropyridine N-oxide;4-chloro-2,3-diMethyl-1$l^{5}-pyridin-1-one;2,3-DiMethyl-4-chloropyridne-n-oxide;4-Chloro-2,3-lutidine N-oxide, 4-Chloro-2,3-dimethylpyridinium-1-olate;nsc 275262;2,3-DIMETHYL-4-CHLOROPYRIDINE-N-OXIDE
CAS:59886-90-7
MF:C7H8ClNO
MW:157.6
EINECS:611-910-8
Product Categories:Nitric Oxide Reagents;Heterocycle-Pyridine series;Rabeprazole;PHARMACEUTICAL INTERMEDIATES;Pyridines;Intermediates of Rabeprazole;Heterocycles;bc0001
Mol File:59886-90-7.mol
4-Chloro-2,3-dimethylpyridine 1-oxide Structure
4-Chloro-2,3-dimethylpyridine 1-oxide Chemical Properties
Melting point 103-105°C
Boiling point 338.5°C
density 1.19
vapor pressure 0.346Pa at 25℃
Fp 158.5°C
storage temp. Room temperature.
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka1.28±0.10(Predicted)
color Pale Yellow to Light Beige
LogP0.4 at 25℃
CAS DataBase Reference59886-90-7(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
HS Code 29333990
MSDS Information
4-Chloro-2,3-dimethylpyridine 1-oxide Usage And Synthesis
Chemical PropertiesPale Yellow Solid
UsesAn intermediate in the synthesis of rabeprazole (R070500).
Synthesis83.0 g (0.49 mol) of 4-nitro-2,3-dimethylpyridine N-oxide and 90 g (1.54 mol) of NaCl were admixed with 1350 ml of CH3CN, 180 ml of aq. HCl (36%) and 16.6 g of benzyltributylammonium chloride, and the resulting suspension was boiled under reflux with stirring for 12 h. The resulting reaction mixture was adjusted to PH=9 using 350 ml of 20% NaOH, wherefor the existing precipitate largely dissolved. The organic phase was separated off, water was added to the aqueous phase until the precipitate had completely dissolved, and it was subsequently extracted using dichloromethane. The organic phases were combined and the solvent was removed under reduced pressure. 76.6 g (98.5%) of 4-Chloro-2,3-dimethylpyridine 1-oxide were obtained.
4-Chloro-2,3-dimethylpyridine 1-oxide
4-Chloro-2,3-dimethylpyridine 1-oxide Preparation Products And Raw materials
Raw materialsHydrochloric acid-->Ethyl acetate-->Sulfuric acid-->Dichloromethane-->Acetic acid-->Nitric acid-->Hydrogen peroxide-->2,3-Lutidine-->4-Nitro-2,3-lutidine-N-oxide-->2,3-Dimethylpyridine-N-oxide
Tag:4-Chloro-2,3-dimethylpyridine 1-oxide(59886-90-7) Related Product Information
ETHYLENE OXIDE Aluminum oxide Zinc oxide 4-Chloropyridinium chloride 2,6-Lutidine Chlorodimethylphenylsilane tert-Butyldimethylsilyl chloride Clopidol Iron oxide DIMETHYLTHEXYLSILYL CHLORIDE NITRIC OXIDE Pyridine-N-oxide CHLORODIMETHYLVINYLSILANE 2,3-Lutidine Sodium oxide (Diethoxymethyl)diphenylphosphine oxide 4-Chloropyridine N-oxide 2,3-Dimethylpyridine-N-oxide