ChemicalBook--->CAS DataBase List--->28342-75-8

28342-75-8

28342-75-8 Structure

28342-75-8 Structure
IdentificationBack Directory
[Name]

1,5-DIBROMO-2,4-DIFLUOROBENZENE
[CAS]

28342-75-8
[Synonyms]

28342-75-8
1.3-Dibrom-4.6-difluorben
1.3-Dibrom-4.6-difluorbenzol
1,5-DIBROMO-2,4-DIFLUOROBENZENE
1,3-DibroMo-4,6-difluorobenzene
2,4-Difluoro-1,5-dibromobenzene
Benzene, 1,5-dibromo-2,4-difluoro-
1,5-Dibromo-2,4-difluorobenzene 98%
[Molecular Formula]

C6H2Br2F2
[MDL Number]

MFCD08458122
[MOL File]

28342-75-8.mol
[Molecular Weight]

271.886
Chemical PropertiesBack Directory
[Melting point ]

29.0 to 33.0 °C
[Boiling point ]

100℃ (25 Torr)
[density ]

2.087±0.06 g/cm3(Predicted)
[storage temp. ]

Room temperature.
[form ]

powder to lump
[color ]

White to Almost white
[InChI]

InChI=1S/C6H2Br2F2/c7-3-1-4(8)6(10)2-5(3)9/h1-2H
[InChIKey]

PPUZKAPOPPRMFE-UHFFFAOYSA-N
[SMILES]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[HS Code ]

2903998090
Spectrum DetailBack Directory
[Spectrum Detail]

1,5-DIBROMO-2,4-DIFLUOROBENZENE(28342-75-8)1HNMR
1,5-DIBROMO-2,4-DIFLUOROBENZENE(28342-75-8)FT-IR
Hazard InformationBack Directory
[Synthesis]

1-Bromo-2,4-difluorobenzene

348-57-2

1,5-DIBROMO-2,4-DIFLUOROBENZENE

28342-75-8

General procedure for the synthesis of 1,5-dibromo-2,4-difluorobenzene from 2,4-difluorobromobenzene: Iron powder (3.15 g, 56 mmol) was added to a solution of 1-bromo-2,4-difluorobenzene (19.3 mL, 171 mmol) in dichloromethane (100 mL). A dichloromethane (25 mL) solution of bromine (11 mL, 214 mmol) was slowly added dropwise to the stirred suspension over 30 minutes. The reaction mixture was stirred overnight at room temperature. Subsequently, the reaction mixture was slowly poured into saturated aqueous sodium thiosulfate solution (200 mL) and stirring was continued for 30 minutes at room temperature. The reaction mixture was extracted with dichloromethane (3 x 80 mL). The organic phases were combined, washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 1,5-dibromo-2,4-difluorobenzene (40 g, 86% yield) as a brown oil.1H NMR (500 MHz, chloroform-d) δ 7.79 (t, J = 7.0 Hz, 1H), 7.00 (t, J = 8.2 Hz, 1H).

[References]

[1] Journal of Organic Chemistry, 2004, vol. 69, # 6, p. 1967 - 1971
[2] Patent: WO2012/162334, 2012, A1. Location in patent: Page/Page column 38
[3] Patent: WO2014/98831, 2014, A1. Location in patent: Page/Page column 26; 27
[4] Nucleosides, Nucleotides and Nucleic Acids, 2001, vol. 20, # 1-2, p. 11 - 40
[5] Patent: EP1961743, 2008, A1. Location in patent: Page/Page column 19
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