Basic information Safety Supplier Related

5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE

Basic information Safety Supplier Related

5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Basic information

Product Name:
5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE
Synonyms:
  • 1-(5-BROMO-2-HYDROXY-3-NITROPHENYL)ETHANONE
  • 3-BROMO-6-HYDROXY-5-NITRO ACETOPHENONE
  • 5-BROMO-2-HYDROXY-3-NITROACETOPHENONE
  • JRH-01018, 1-(5-Bromo-2-hydroxy-3-nitrophenyl)ethanone, 97%
  • 5'-Bromo-2'-hydroxy-3'-nitroacetophenone >
  • Ethanone, 1-(5-bromo-2-hydroxy-3-nitrophenyl)-
  • 1-(5-Bromo-2-hydroxy-3-nitrophenyl)ethan-1-one
  • 5'-Bromo-2'-hydroxy-3'-nitroacetophenone
CAS:
70978-54-0
MF:
C8H6BrNO4
MW:
260.04
Product Categories:
  • Aromatic Acetophenones & Derivatives (substituted)
  • Building Blocks
  • C7 to C8
  • Carbonyl Compounds
  • Chemical Synthesis
  • Ketones
  • Organic Building Blocks
Mol File:
70978-54-0.mol
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5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Chemical Properties

Melting point:
129-132 °C(lit.)
Boiling point:
272.9℃
Density 
1.763
Flash point:
118.9℃
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
6.47±0.38(Predicted)
color 
Light yellow to Yellow to Orange
CAS DataBase Reference
70978-54-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29145090

MSDS

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5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Usage And Synthesis

Uses

5'-Bromo-2'-hydroxy-3'-nitroacetophenone is used as a chemical reagent in the synthesis of amides and benzoxazoles directly using a sulfate catalyst and microwaves. 1-(5-Bromo-2-hydroxy-3-nitrophen yl)ethanone is used in studies involving HIV-1 integrase inhibitors.

Preparation

Preparation by nitration of 5-bromo-2-hydroxyacetophenone in refluxing carbon tetrachloride (88%).

Synthesis

1450-75-5

70978-54-0

1. Synthesis of 5-bromo-2-hydroxy-3-nitroacetophenone To a solution of 5-bromo-2-hydroxyacetophenone (23.7 g, 0.110 mol) in carbon tetrachloride (90 mL) was slowly added concentrated nitric acid (17.2 mL). The reaction mixture was stirred at 75 °C for 50 min and subsequently cooled to room temperature. The precipitated solid was collected by filtration and washed with cold carbon tetrachloride. After vacuum drying, 20.9 g of the target product 5-bromo-2-hydroxy-3-nitroacetophenone was obtained as a light yellow solid in 73% yield. 1H NMR (300 MHz, CDCl3) δ: 2.73 (s, 3H), 8.14 (d, 1H), 8.31 (d, 1H), 12.92 (s, 1H).

References

[1] Patent: US5990142, 1999, A
[2] Patent: EP1391451, 2004, A1. Location in patent: Page 113
[3] Patent: WO2017/221002, 2017, A1. Location in patent: Page/Page column 92

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