4-BROMO-6-FLUOROINDAN-1-ONE

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Products Intro: Product Name:4-Bromo-6-fluoro-1-indanone
CAS:174603-56-6
Purity:99% Package:1KG,5KG,10KG
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Products Intro: Product Name:4-Bromo-6-fluoro-2,3-dihydro-1H-inden-1-one
CAS:174603-56-6
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CAS:174603-56-6
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Products Intro: Product Name:4-Bromo-6-fluoro-1-indanone
CAS:174603-56-6
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Products Intro: Product Name:4-Bromo-6-fluoro-2,3-dihydroinden-1-one
CAS:174603-56-6
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4-BROMO-6-FLUOROINDAN-1-ONE manufacturers

4-BROMO-6-FLUOROINDAN-1-ONE Basic information
Product Name:4-BROMO-6-FLUOROINDAN-1-ONE
Synonyms:4-BROMO-6-FLUOROINDAN-1-ONE;1H-Inden-1-one,4-broMo-6-fluoro-2,3-dihydro-;4-Bromo-6-fluoro-1-indanone;4-broMo-6-fluoro-2,3-dihydro-1H-inden-1-one;4-bromo-6-fluoro-2,3-dihydroinden-1-one
CAS:174603-56-6
MF:C9H6BrFO
MW:229.05
EINECS:
Product Categories:
Mol File:174603-56-6.mol
4-BROMO-6-FLUOROINDAN-1-ONE Structure
4-BROMO-6-FLUOROINDAN-1-ONE Chemical Properties
Boiling point 301.1±42.0 °C(Predicted)
density 1.691±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceWhite to light brown Solid
InChIInChI=1S/C9H6BrFO/c10-8-4-5(11)3-7-6(8)1-2-9(7)12/h3-4H,1-2H2
InChIKeyKBBCLUTZUIWTON-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C(Br)=CC(F)=C2)CC1
Safety Information
HS Code 2914790090
MSDS Information
4-BROMO-6-FLUOROINDAN-1-ONE Usage And Synthesis
Synthesis
3-(2-BROMO-4-FLUORO-PHENYL)-PROPIONIC ACID

174603-55-5

4-BROMO-6-FLUOROINDAN-1-ONE

174603-56-6

Under argon protection, 3-(2-bromo-4-fluorophenyl)propionic acid (1.2 g) was added to trifluoromethanesulfonic acid (15 mL) in batches and the reaction was carried out at room temperature. Subsequently, the reaction mixture was stirred at 60°C for 2 hours, then warmed to 80°C and continued stirring for 16 hours. After completion of the reaction, it was cooled to room temperature and the mixture was slowly poured into ice water. The aqueous phase was extracted twice with ethyl acetate. The organic phase was combined and washed sequentially with saturated aqueous Na2CO3 and brine. The organic phase was dried over anhydrous MgSO4 and concentrated under reduced pressure to remove the solvent. The resulting residue was stirred with dichloromethane (40 mL), filtered and washed with dichloromethane. The dichloromethane phase was combined and concentrated to give the target compound 4-bromo-6-fluoro-2,3-dihydro-1H-inden-1-one. Yield: 970 mg; liquid chromatography (Method 3): tR = 0.60 min; mass spectrometry (ESI+): m/z = 229 [M + H]+.

References[1] Journal of Medicinal Chemistry, 2003, vol. 46, # 3, p. 409 - 416
[2] Patent: WO2013/144098, 2013, A1. Location in patent: Page/Page column 114; 115
[3] Patent: WO2015/36759, 2015, A1
4-BROMO-6-FLUOROINDAN-1-ONE Preparation Products And Raw materials
Raw materials3-(2-BROMO-4-FLUORO-PHENYL)-PROPIONIC ACID-->2-Bromo-1-(bromomethyl)-4-fluorobenzene-->2-Bromo-4-fluorotoluene
Tag:4-BROMO-6-FLUOROINDAN-1-ONE(174603-56-6) Related Product Information
4-Bromo-1-indanone 4-BROMO-7-CHLORO-1-INDANONE 4-broMo-7-fluoro-2,3-dihydroinden-1-one 4-Bromo-7-methoxy-indan-1-one 4-Bromo-5-chloro-2,3-dihydro-1H-inden-1-one 4-Isopropylphenol 1H-Inden-1-one, 6-broMo-5-chloro-2,3-dihydro- 6-Chloro-5-fluoro-2,3-dihydro-1H-inden-1-one 4-BROMO-2,3-DIHYDRO-1H-INDEN-1-OL 4,6-dimethyl-1H-indene 6-Fluoro-1-indanone 4-BROMO-6-FLUORO-7-HYDROXY-3-METHYLINDAN-1-ONE 4-BROMO-6-FLUOROINDAN-1-ONE

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