Basic information Safety Supplier Related

4-Bromoisatoic anhydride

Basic information Safety Supplier Related

4-Bromoisatoic anhydride Basic information

Product Name:
4-Bromoisatoic anhydride
Synonyms:
  • 7-Bromo-1H-benzo[d][1,3]oxazine-2,4-dione
  • 7-Bromo-2H-3,1-benzoxazine-2,4(1H)-dione
  • 4-Bromo-isatoic anhydride
  • 4-Bromoisatoic anhydride 97%
  • 7-Bromo-2H-3,1-benzoxazine-2,4(1H)-dione, 7-Bromo-1H-benzo[d][1,3]oxazine-2,4-dione
  • 4-Bromoisatoicanhydride97%
  • Isatoic anhydride, 4-bromo-
  • 7-bromo-1H-3,1-benzoxazine-2,4-dione
CAS:
76561-16-5
MF:
C8H4BrNO3
MW:
242.03
Mol File:
76561-16-5.mol
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4-Bromoisatoic anhydride Chemical Properties

Density 
1.826
storage temp. 
2-8°C
form 
Pale cream, wooly, small crystalline flakes
pka
9.95±0.20(Predicted)
Appearance
Off-white to light yellow Solid
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Safety Information

HS Code 
2934999090
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4-Bromoisatoic anhydride Usage And Synthesis

Chemical Properties

White solid

Synthesis

32315-10-9

20776-50-5

76561-16-5

7.1: Synthesis of 7-bromo-1H-benzo[d][1,3]oxazine-2,4-dione In a 250 mL round bottom flask, 5.0 g (23.1 mmol) of 2-amino-4-bromobenzoic acid was dissolved in 50 mL of anhydrous dioxane under nitrogen protection. The reaction mixture was cooled to 0 °C via an ice bath. 2.3 g (7.6 mmol) of triphosgene was added slowly and dropwise. Subsequently, the ice bath was replaced with an oil bath and the reaction mixture was refluxed for 16 hours. After completion of the reaction, it was cooled to room temperature, 100 mL of water was added, and the resulting precipitate was collected by filtration. The precipitate was washed with ether (3 x 25 mL) and then dried in an oven to give 5.6 g (23.1 mmol) of the target product as a beige powder in 100% yield. 1H NMR (DMSO-d6, 300 MHz) δ: 7.29 (d, J = 1.8 Hz, 1H), 7.41 (dd, J = 8.4 Hz, J = 1.8 Hz, 1H), 7.82 (d, J = 8.4 Hz, 1H), 11.81 (bs, 1H).

References

[1] Patent: US2011/251194, 2011, A1. Location in patent: Page/Page column 17
[2] Patent: WO2013/147711, 2013, A1. Location in patent: Page/Page column 158
[3] Patent: US2014/371199, 2014, A1. Location in patent: Paragraph 0584
[4] Beilstein Journal of Organic Chemistry, 2018, vol. 14, p. 2529 - 2536
[5] Journal of Medicinal Chemistry, 2015, vol. 58, # 17, p. 6928 - 6937

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