ChemicalBook--->CAS DataBase List--->10495-73-5

10495-73-5

10495-73-5 Structure

10495-73-5 Structure
IdentificationBack Directory
[Name]

6-BROMO-2,2'-BIPYRIDINE
[CAS]

10495-73-5
[Synonyms]

6-BroMo-2,2'-bipyridyl
6-BROMO-2,2'-BIPYRIDINE
6-broMo-2,2'-bipyridine 97%
2-BROMO-6-(2-PYRIDYL)PYRIDINE
2-bromo-6-(pyridin-2-yl) pyridine
[Molecular Formula]

C10H7BrN2
[MDL Number]

MFCD01318953
[MOL File]

10495-73-5.mol
[Molecular Weight]

235.08
Chemical PropertiesBack Directory
[Melting point ]

72.0 to 76.0 °C
[Boiling point ]

133°C/2.2mmHg(lit.)
[density ]

1.493±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Chloroform, Methanol
[form ]

powder to crystal
[pka]

3.70±0.22(Predicted)
[color ]

White to Almost white
[BRN ]

130238
[InChI]

InChI=1S/C10H7BrN2/c11-10-6-3-5-9(13-10)8-4-1-2-7-12-8/h1-7H
[InChIKey]

NCRIDSGPLISUEU-UHFFFAOYSA-N
[SMILES]

C1(C2=NC=CC=C2)=NC(Br)=CC=C1
[CAS DataBase Reference]

10495-73-5
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22-36/37/38-22
[Safety Statements ]

26-36/37/39
[RIDADR ]

UN 2811
[WGK Germany ]

3
[HazardClass ]

6.1
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

6-Bromo-2,2’-bipyridine is a reagent used in the synthesis of electron transporting layers for OLEDs.
[Synthesis]

2,6-Dibromopyridine

626-05-1

2-(TRIBUTYLSTANNYL)PYRIDINE

17997-47-6

6-BROMO-2,2'-BIPYRIDINE

10495-73-5

General procedure for the synthesis of 6-bromo-2,2'-bipyridine from 2,6-dibromopyridine and 2-tributylmethylstannylpyridine: 1.5 g (6.33 mmol) of 2,6-dibromopyridine, 3.48 g (9.48 mmol) of 2-tributylmethylstannylpyridine and 0.15 g (0.06 mmol) of tetrakis(triphenylphosphine)palladium (Pd(PPh3)4) were were dissolved in 15 mL of toluene in a two-necked round bottom flask. The reaction mixture was stirred at 80°C for about 24 hours. Upon completion of the reaction, the solvent was removed by evaporation under reduced pressure. The resulting residue was dissolved in dichloromethane and subsequently extracted with 6M hydrochloric acid solution. The aqueous layer was separated and collected, the pH was adjusted by adding ammonia to the aqueous layer and extracted with dichloromethane. The organic layer was separated and dried with anhydrous magnesium sulfate (MgSO4) followed by evaporation under reduced pressure to remove the solvent. Purification by column chromatography (eluent: hexane/ethyl acetate=5:1, v/v) afforded 0.9 g of 6-bromo-2,2'-bipyridine as a white solid (yield: 61%).

[References]

[1] Organic Letters, 2008, vol. 10, # 6, p. 1091 - 1094
[2] Chemical Communications, 2007, # 42, p. 4401 - 4403
[3] Organometallics, 2017, vol. 36, # 9, p. 1727 - 1735
[4] Patent: KR2015/142709, 2015, A. Location in patent: Paragraph 0473-0475
[5] Inorganic Chemistry, 2013, vol. 52, # 9, p. 5570 - 5580
Spectrum DetailBack Directory
[Spectrum Detail]

6-BROMO-2,2'-BIPYRIDINE(10495-73-5)1HNMR
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