Basic information Safety Supplier Related

6-BROMO-2-METHYL-3,4-DIHYDROQUINAZOLIN-4-ONE

Basic information Safety Supplier Related

6-BROMO-2-METHYL-3,4-DIHYDROQUINAZOLIN-4-ONE Basic information

Product Name:
6-BROMO-2-METHYL-3,4-DIHYDROQUINAZOLIN-4-ONE
Synonyms:
  • 6-BROMO-2-METHYL-3,4-DIHYDROQUINAZOLIN-4-ONE
  • 6-bromo-2-methyl-1H-quinazolin-4-one
  • 6-bromo-2-methylquinazolin-4(3H)-one(SALTDATA: FREE)
  • 6-broMo-2-Methylquinazolin-4-ol
  • 6-bromo-2-methylquinazolin-4(1H)-one
  • 6-bromo-2-methyl-4(3H)-Quinazolinone
  • 4(1H)-Quinazolinone, 6-bromo-2-methyl-
  • 4(3H)-Quinazolinone, 6-bromo-2-methyl-
CAS:
5426-59-5
MF:
C9H7BrN2O
MW:
239.07
Mol File:
5426-59-5.mol
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6-BROMO-2-METHYL-3,4-DIHYDROQUINAZOLIN-4-ONE Chemical Properties

Melting point:
298 °C
Boiling point:
372.6±44.0 °C(Predicted)
Density 
1.72±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
1.96±0.20(Predicted)
Appearance
Off-white to light brown Solid
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Safety Information

Risk Statements 
22
Safety Statements 
36/37
HS Code 
29339900
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6-BROMO-2-METHYL-3,4-DIHYDROQUINAZOLIN-4-ONE Usage And Synthesis

Chemical Properties

Light yellow solid

Synthesis

108-24-7

5794-88-7

5426-59-5

The general procedure for the synthesis of 6-bromo-2-methylquinazolin-4(3H)-one from ethanoic anhydride and 2-amino-5-bromobenzoic acid was as follows: first, 2-amino-5-bromobenzoic acid was refluxed for 1 h in liquid ammonia (10 mL/g). Subsequently, the reaction solution was concentrated to a smaller volume and the residue was mixed with acetic anhydride (2 mL/g) and refluxing was continued for 4 hours. Upon completion of the reaction, water was added to the mixture and boiled for 30 minutes, followed by dropwise addition of 20% sodium hydroxide solution until a clarified solution was formed. Next, ammonium carbonate was added to the hot solution until a precipitate was formed. The mixture was allowed to stand at 4°C for 16 hours, after which the precipitate was collected by filtration, washed with water and finally dried under vacuum to give the target product in about 60% yield.

References

[1] Patent: US2009/69320, 2009, A1. Location in patent: Page/Page column 76
[2] Journal of the American Chemical Society, 1906, vol. 28, p. 101

6-BROMO-2-METHYL-3,4-DIHYDROQUINAZOLIN-4-ONESupplier

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