ChemicalBook--->CAS DataBase List--->16372-96-6

16372-96-6

16372-96-6 Structure

16372-96-6 Structure
IdentificationBack Directory
[Name]

3,5-DibroMo-biphenyl
[CAS]

16372-96-6
[Synonyms]

PBB 14
3,5-DibroMo-biphenyl
3,5-DIBROMO-1-PHENYLBENZENE
1,1'-Biphenyl, 3,5-dibromo-
[Molecular Formula]

C12H8Br2
[MDL Number]

MFCD00143073
[MOL File]

16372-96-6.mol
[Molecular Weight]

312
Chemical PropertiesBack Directory
[Melting point ]

156-157℃
[Boiling point ]

208 °C(Press: 15 Torr)
[density ]

1.7197 g/cm3(Temp: 25 °C)
[refractive index ]

1.6541 (589.3 nm 25℃)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

crystalline solid
[color ]

White
[InChI]

InChI=1S/C12H8Br2/c13-11-6-10(7-12(14)8-11)9-4-2-1-3-5-9/h1-8H
[InChIKey]

HIHYAKDOWUFGBK-UHFFFAOYSA-N
[SMILES]

C1(C2=CC=CC=C2)=CC(Br)=CC(Br)=C1
[EPA Substance Registry System]

1,1'-Biphenyl, 3,5-dibromo- (16372-96-6)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P280-P302+P352-P362+P364
[HS Code ]

2903998090
Hazard InformationBack Directory
[Chemical Properties]

Colorless liquid
[Synthesis]

1,3,5-Tribromobenzene

626-39-1

Phenylboronic acid

98-80-6

3,5-DibroMo-biphenyl

16372-96-6

A suspension of EtOH-H2O (3 mL, v:v = 1:1) with 1,3,5-tribromobenzene (1.0 mmol), phenylboronic acid (1.2 mmol), potassium carbonate (276 mg, 2.0 mmol), and Pd/HCCP-DABP catalyst (20 mg, 0.3 mol%) was added to the Schlenk tube. The system was evacuated and backfilled three times with nitrogen. The reaction mixture was stirred at 50 °C for 2.5 hours. After completion of the reaction, it was cooled to room temperature and extracted with dichloromethane (CH2Cl2). The organic phases were combined, dried with anhydrous sodium sulfate, concentrated under reduced pressure and purified by silica gel column chromatography to give 1-phenyl-3,5-dibromobenzene. The aqueous phase was filtered through filter paper, the solid was washed with CH2Cl2, and the recovered catalyst could be used in subsequent reactions.

[References]

[1] Reactive and Functional Polymers, 2017, vol. 110, p. 38 - 46
[2] Patent: KR2016/69021, 2016, A. Location in patent: Paragraph 0155-0157
[3] Journal of the American Chemical Society, 1990, vol. 112, # 22, p. 8024 - 8034
[4] Patent: KR2015/53913, 2015, A. Location in patent: Paragraph 0533-0535
[5] Patent: KR2015/127023, 2015, A. Location in patent: Paragraph 0409; 0560; 0561; 0562; 0563; 0564
Spectrum DetailBack Directory
[Spectrum Detail]

3,5-DibroMo-biphenyl(16372-96-6)1HNMR
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