Basic information Safety Supplier Related

2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-

Basic information Safety Supplier Related

2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO- Basic information

Product Name:
2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-
Synonyms:
  • 2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO-
  • 5-Bromo-1,3-dihydro-2H-inden-2-one
  • 5-Bromoindan-2-one
  • 2-Indanone, 5-broMo-
  • 5-bromo-1,3-dihydroinden-2-one
  • 5-BROMO-1H-INDEN-2(3H)-ONE
  • 5-Bromo-2-indanone
  • 5-broMo-2,3-dihydro-1H-inden-2-one
CAS:
174349-93-0
MF:
C9H7BrO
MW:
211.06
Mol File:
174349-93-0.mol
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2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO- Chemical Properties

Boiling point:
299.5±40.0 °C(Predicted)
Density 
1.608±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to yellow Solid
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Safety Information

HS Code 
2914390090
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2H-INDEN-2-ONE, 5-BROMO-1,3-DIHYDRO- Usage And Synthesis

Synthesis

75476-78-7

174349-93-0

The general procedure for the synthesis of 5-bromo-2-indanone from 5-bromo-1H-indene was as follows: first, 1.5 L of 30% H2O2 and 300 mL of formic acid were added to a reaction flask, and the temperature of the reaction was controlled at 35 °C. Subsequently, 148 g of 5-bromo-1H-indene was added to the reaction mixture at 40 °C. The reaction mixture was stirred at room temperature for 12 hours. Upon completion of the reaction, a large amount of water was added to the reaction mass to precipitate a white solid, which was subsequently filtered. Next, 3 L of 5% aqueous sulfuric acid solution was added to the flask and heated to boiling. The white solid reactant was added to the flask and connected to a distillation unit to obtain a final 64 g of 5-bromo-2-indanone (white solid).

References

[1] Patent: JP2016/29040, 2016, A. Location in patent: Paragraph 0060

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