Basic information Safety Supplier Related

10-Methoxycarbamazepine

Basic information Safety Supplier Related

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
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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)
pka
13.86±0.40(Predicted)
form 
Solid
color 
Off-White
CAS DataBase Reference
28721-09-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
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10-Methoxycarbamazepine Usage And Synthesis

Chemical Properties

Off-White Solid

Uses

Intermediate in the preparation of dibenzazepine derivatives.

Synthesis

4698-11-7

32315-10-9

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

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