ChemicalBook--->CAS DataBase List--->125114-77-4

125114-77-4

125114-77-4 Structure

125114-77-4 Structure
IdentificationBack Directory
[Name]

7-Bromo-1-indanone
[CAS]

125114-77-4
[Synonyms]

-broMo-2,3-dihydroinden-1-one
7-bromo-2,3-dihydroinden-1-one
7-bromo-2,3-dihydro-1H-inden-1-one
1H-Inden-1-one,7-broMo-2,3-dihydro-
7-Bromo-2,3-dihydro-1H-inden-1-one, 7-Bromo-2,3-dihydro-1-oxo-1H-indene
[Molecular Formula]

C9H7BrO
[MDL Number]

MFCD06796574
[MOL File]

125114-77-4.mol
[Molecular Weight]

211.05
Chemical PropertiesBack Directory
[Melting point ]

114 °C
[Boiling point ]

306.5±31.0 °C(Predicted)
[density ]

1.608±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

solid
[color ]

Yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2914390090
Questions And AnswerBack Directory
[Application]

7-Bromo-1-indanones are an important class of compounds, frequently used as intermediates in pharmaceuticals and natural products. Indanone structures are widely found in many natural products of plant and marine origin and possess good biological activity, such as indanoxyacetic acid compounds with diuretic and salt-excreting effects. Indanones are also intermediates in the synthesis of many drugs, such as rasagiline hydrochloride, an anti-Parkinson's drug, and can serve as the backbone for antidepressants and tranquilizers.
Spectrum DetailBack Directory
[Spectrum Detail]

7-Bromo-1-indanone(125114-77-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

To a stirring solution of 7-Amino-2,3-dihydroinden-1-one (1.0 g, 6.8 mmol) in 48 % HBraq (2 mL) and EtOH (8 mL) was added NaNO2 (0.62 g, 8.6 mmol) dissolved in H20 (1 mL) at 0 °C and kept at 0 °C for 15 mm. Then a solution of CuBr (0.54 g, 3.6 mmol) in 48percent HBraq (8 mL) was added to the mixture at95 °C and kept at 95 °C for 15 mm. After consumption of the starting material (by TLC), the reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with saturated NaHCO3 aq. Combined organic extracts were dried over anhydrous Na2504 and concentrated under reduced pressure to obtain a crude product, which was purified by silica gel column chromatography eluting with 10 % EtOAc /PE to afford 7-Bromo-1-indanone (0.54 g, 37 %) as an off-white solid. LC-MS: m/z = 212.0 [M+H]
[References]

[1] Patent: JP2015/63515, 2015, A. Location in patent: Paragraph 0153
[2] Journal of Organic Chemistry, 2003, vol. 68, # 26, p. 10195 - 10198
[3] Patent: US2008/255230, 2008, A1. Location in patent: Page/Page column 20-21
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