10-Methoxycarbamazepine

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Products Intro: CAS:28721-09-7
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CAS:28721-09-7
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Products Intro: Product Name:10-Methoxycarbamazepine
CAS:28721-09-7
Purity:0.99 Package:1kg,5kg,25kgs,200kgs;bulk

10-Methoxycarbamazepine manufacturers

10-Methoxycarbamazepine Basic information
Product Name:10-Methoxycarbamazepine
Synonyms:10-methoxy-5h-dibenz(b,f)azepine-5-carboxamide;10-METHOXY CARBAMAZEPINE;10-METHOXY-5H-DIBENZ[B,F]AZEPINE-5-CARBOXAMIDE 98.5%;10-Methoxy-5H-dibenzo[b,f]azepine-5-carboxaMide;Oxcarbazepine IMpurity C;Oxcarbazepine Impurity 6;Oxcarbazepine Impurity 2(Oxcarbazepine EP Impurity B);Oxcarbazepine-2
CAS:28721-09-7
MF:C16H14N2O2
MW:266.29
EINECS:249-189-3
Product Categories:Amines;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:28721-09-7.mol
10-Methoxycarbamazepine Structure
10-Methoxycarbamazepine Chemical Properties
Melting point 186-188°C
Boiling point 468.0±55.0 °C(Predicted)
density 1.31
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka13.86±0.40(Predicted)
form Solid
color Off-White
Major Applicationpharmaceutical small molecule
CAS DataBase Reference28721-09-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 22
MSDS Information
10-Methoxycarbamazepine Usage And Synthesis
Chemical PropertiesOff-White Solid
UsesIntermediate in the preparation of dibenzazepine derivatives.
Synthesis
10-Methoxyiminostilbene

4698-11-7

Triphosgene

32315-10-9

10-Methoxycarbamazepine

28721-09-7

1. 32.67 g (0.11 mol) of triphosgene dissolved in 300 mL of toluene was slowly added dropwise over a period of 6 hours to a mixture of 66.9 g (0.3 mol) of 10-methoxy-5H-dibenzo[b,f]azepine and 34.92 g (0.34 mol) of triethylamine in 800 mL of toluene at a temperature of 10-15 °C. 2. After completion of the reaction ( complete disappearance of 10-methoxy-5H-dibenz[b,f]azepine was confirmed by TLC monitoring), 200 mL of 30% ammonia was slowly added with vigorous stirring for several hours at room temperature.3. After the reaction mixture was layered, the organic phase was separated, the toluene phase was washed with water, and the reaction mixture was subsequently evaporated to dryness under reduced pressure.4. 69.0 g (85% of the theoretical yield) was obtained of a purity greater than 95% of 10-methoxy-5H-dibenz[b,f]azepine. Methoxy-5H-dibenz[b,f]azepine-5-carboxamide.

References[1] Patent: EP1600443, 2005, A1. Location in patent: Page/Page column 8
Tag:10-Methoxycarbamazepine(28721-09-7) Related Product Information
Benzamide Carbamazepine 2-Methoxyethanol Chlorantraniliprole 10-Methoxyiminostilbene Methoxy 10-Methoxycarbamazepine