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625446-22-2

625446-22-2 Structure

625446-22-2 Structure
IdentificationBack Directory
[Name]

4-BROMO-2-FLUOROACETOPHENONE
[CAS]

625446-22-2
[Synonyms]

4-BROMO-2-FLUOROACETOPHENONE
2-Fluoro-4-bromoacetophenone
4'-BROMO-2'-FLUOROACETOPHENONE
1-Acetyl-4-bromo-2-fluorobenzene
4'-Bromo-2'-fluoroacetophenone98%
4'-Bromo-2'-fluoroacetophenone 98%
4'-Bromo-2'-fluoroacetophenone,96%
1-(4-Bromo-2-fluorophenyl)ethan-1-one
1-(4-broMophenyl)-2-fluoroethan-1-one
Ethanone, 1-(4-broMo-2-fluorophenyl)-
4-Bromo-2-fluoroacetophenone/2-Fluoro-4-bromoacetophenone
[EINECS(EC#)]

205-516-1
[Molecular Formula]

C8H6BrFO
[MDL Number]

MFCD03411551
[MOL File]

625446-22-2.mol
[Molecular Weight]

217.04
Chemical PropertiesBack Directory
[Melting point ]

23 °C
[Boiling point ]

256.3±25.0 °C(Predicted)
[density ]

1.535±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Acetonitrile (Slightly), Chloroform (Slightly)
[form ]

Solid
[color ]

White to Off-White
[InChI]

InChI=1S/C8H6BrFO/c1-5(11)7-3-2-6(9)4-8(7)10/h2-4H,1H3
[InChIKey]

ASKFCSCYGAFWAB-UHFFFAOYSA-N
[SMILES]

C(=O)(C1=CC=C(Br)C=C1F)C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H319
[Precautionary statements ]

P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38-36
[Safety Statements ]

26-36/37/39
[WGK Germany ]

WGK 3
[Hazard Note ]

Irritant
[HS Code ]

2914790090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Spectrum DetailBack Directory
[Spectrum Detail]

4-BROMO-2-FLUOROACETOPHENONE(625446-22-2)1HNMR
4-BROMO-2-FLUOROACETOPHENONE(625446-22-2)FT-IR
Hazard InformationBack Directory
[Synthesis]

To a solution of 4-bromo-2-fluoro-N-methoxy-N-methylbenzamide (13 g, 46 mmol) in THF (4.0 mL) was added dropwise methylmagnesium bromide (3M ethyl ether solution, 30 mL, 91 mmol) at 0°C, and the mixture was stirred at room temperature for 3 hr. For the reaction mixture, saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The obtained extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give 4-Bromo-2-fluoroacetophenone as a pale yellow oil.
[References]

[1] Patent: US2008/45556, 2008, A1. Location in patent: Page/Page column 32
[2] Patent: US2011/118257, 2011, A1. Location in patent: Page/Page column 97-98
[3] Patent: US2011/281865, 2011, A1. Location in patent: Page/Page column 85-86
[4] Patent: WO2011/145035, 2011, A1. Location in patent: Page/Page column 114-115
[5] Journal of Medicinal Chemistry, 2008, vol. 51, # 2, p. 282 - 297
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