ChemicalBook--->CAS DataBase List--->23674-20-6

23674-20-6

23674-20-6 Structure

23674-20-6 Structure
IdentificationBack Directory
[Name]

9-Bromo-10-phenylanthracene
[CAS]

23674-20-6
[Synonyms]

9-Bromo-10-phenyl
9-Bromo-10-phenylant
9-bromo-10-phenylindole
10-broMo-9-phenylanthracene
9-Bromo-10-phenylanthracene
10-phenyl-9-BroMoanthracene
9-bromo-10-phenylanthrancene
Anthracene, 9-Bromo-10-phenyl
9-Bromo-10-phenylanthracene >
9-Bromo-10-phenylanthracene,98%
9-Bromo-10-phenylanthracene ISO 9001:2015 REACH
[EINECS(EC#)]

621-755-8
[Molecular Formula]

C20H13Br
[MDL Number]

MFCD00230983
[MOL File]

23674-20-6.mol
[Molecular Weight]

333.22
Chemical PropertiesBack Directory
[Melting point ]

154-155 °C
[Boiling point ]

449.7±14.0 °C(Predicted)
[density ]

1.393
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform, Methanol (Slightly)
[form ]

Powder
[color ]

Pale yellow
[Water Solubility ]

Insoluble in water. Soluble in hot toluene, dimethylformamide.
[InChI]

InChI=1S/C20H13Br/c21-20-17-12-6-4-10-15(17)19(14-8-2-1-3-9-14)16-11-5-7-13-18(16)20/h1-13H
[InChIKey]

WHGGVVHVBFMGSG-UHFFFAOYSA-N
[SMILES]

C1=C2C(C(C3=CC=CC=C3)=C3C(=C2Br)C=CC=C3)=CC=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H317-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Safety Statements ]

24/25
[HS Code ]

29039990
Hazard InformationBack Directory
[Description]

9-Bromo-10-phenylanthracene is a yellow-white solid powder that is commonly used as an organic synthesis intermediate.It is not soluble in water but can dissolve in dimethyl sulfoxide, N,N-dimethylformamide, and other polar solvents. It is also soluble in hot non-polar solvents due to its low polarity.
[Chemical Properties]

Pale yellow powder
[Uses]

It is used as an OLED material.
Questions And Answer(Q&A)Back Directory
[Preparation]

9-Phenylanthracene (2.5g, 9.83mmol) and NBS (2.1g, 11.8mmol) were dissolved in 80mL CHCl3. Then the mixture was heated to 60°C for 2h under N2. After cooled to room temperature, 20 mL water was added. And the mixture was extracted with CH2Cl2. The organic extracts were dried over anhydrous MgSO4 and concentrated by rotary evaporation.The crude product was recrystallized from methanol to get a green-yellow powder (2g, 61.2%). 1H NMR (500 MHz, CDCl3) δ 8.67 – 8.61 (m, 2H), 7.71 – 7.65 (m, 2H), 7.64 – 7.56 (m, 5H), 7.45 – 7.37 (m, 4H). EI-MS (m/z): Calculated for C20H13Br: 333.22. Found [M+]: 332.30.
preparation of 9-bromo-10-phenylanthracene
Synthesis of 9-bromo-10-phenylanthracene
Spectrum DetailBack Directory
[Spectrum Detail]

9-Bromo-10-phenylanthracene(23674-20-6)1HNMR
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