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ChemicalBook > CAS DataBase List > 2-Bromo-9,10-bis(2-naphthalenyl)anthracene

2-Bromo-9,10-bis(2-naphthalenyl)anthracene

Application
Product Name
2-Bromo-9,10-bis(2-naphthalenyl)anthracene
CAS No.
474688-76-1
Chemical Name
2-Bromo-9,10-bis(2-naphthalenyl)anthracene
Synonyms
BDNA;2-BR-ADN;2-Bromo-9,10-bis(2-;2-Bromo-9,10-bis(2-naphthalenyl);2-Bromo-9,10-di-2-phthalenylanthracene;2-Bromo-9,10-bis(2-naphthyl)anthracene;2-BroMo-9,10-di(2-naphthyl) anthracene;2-broMine-9,10-di-2'naphthylanthracene;2-broMo-9,10-di(phthalen-2-yl)anthracene;2-BroMo-9,10-bis(2-napthalenyl)anthracene
CBNumber
CB41512388
Molecular Formula
C34H21Br
Formula Weight
509.43
MOL File
474688-76-1.mol
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2-Bromo-9,10-bis(2-naphthalenyl)anthracene Property

Boiling point:
630.1±24.0 °C(Predicted)
Density 
1.367±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
color 
White to Yellow to Green
InChI
InChI=1S/C34H21Br/c35-28-17-18-31-32(21-28)34(27-16-14-23-8-2-4-10-25(23)20-27)30-12-6-5-11-29(30)33(31)26-15-13-22-7-1-3-9-24(22)19-26/h1-21H
InChIKey
NNVPXSAMRFIMLP-UHFFFAOYSA-N
SMILES
C1=C2C(C(C3=CC=C4C(=C3)C=CC=C4)=C3C(=C2C2=CC=C4C(=C2)C=CC=C4)C=CC=C3)=CC=C1Br
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Safety

HS Code 
2903.99.8001
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TCI Chemical
Product number
B4321
Product name
2-Bromo-9,10-di(2-naphthyl)anthracene
Purity
>98.0%(HPLC)
Packaging
1g
Price
$55
Updated
2024/03/01
TCI Chemical
Product number
B4321
Product name
2-Bromo-9,10-di(2-naphthyl)anthracene
Purity
>98.0%(HPLC)
Packaging
5g
Price
$166
Updated
2024/03/01
TRC
Product number
B695668
Product name
2-Bromo-9,10-bis(2-naphthalenyl)anthracene
Packaging
500mg
Price
$125
Updated
2021/12/16
AK Scientific
Product number
J97730
Product name
2-Bromo-9,10-bis(2-naphthalenyl)anthracene
Packaging
10g
Price
$155
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB29216
Product name
2-Bromo-9,10-bis(2-naphthalenyl)anthracene
Packaging
1g
Price
$160
Updated
2021/12/16
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2-Bromo-9,10-bis(2-naphthalenyl)anthracene Chemical Properties,Usage,Production

Application

2-Bromo-9,10-bis(2-naphthyl)anthracene is a fused-ring compound with a large conjugated system in its molecular structure, and it has wide applications in organic light-emitting materials and organic conductive materials.

Chemical Properties

Yellow green powder

Synthesis

474688-75-0

474688-76-1

The general procedure for the synthesis of 2-bromo-9,10-bis(2-naphthalenyl)anthracene from 2-bromo-9,10-bis(2-naphthalenyl)anthracene-9,10-diol was as follows: compound 109 (2-bromonaphthalene, 11.0 g, 53.1 mmol) was dissolved in anhydrous tetrahydrofuran (100 mL) under nitrogen protection. The solution was cooled to -78 °C in a cooling bath, followed by the slow addition of tert-butyl lithium (47.0 mL, 1.7 M pentane solution). The reaction mixture was stirred for about 1 hour while maintaining -78 °C, followed by the addition of compound 104 (6.31 g, 22.0 mmol). The cooling bath was removed and the reaction mixture was allowed to warm up to room temperature and stirring was continued for about 3 hours. Upon completion of the reaction, the reaction was quenched by addition of aqueous ammonium chloride to the mixture and extracted with dichloromethane. The organic phases were combined, dried with magnesium sulfate and concentrated under reduced pressure to give the crude product. The crude product was dissolved in ether, crystallization was induced by the addition of petroleum ether, and the solid was collected by filtration after stirring for several hours and dried under vacuum to give dinaphthalenyl glycol (11.2 g, 93% yield). Next, dinaphthyl glycol (11.2 g, 20.5 mmol) was suspended in acetic acid (600 mL) under nitrogen protection and potassium iodide (34.2 g, 206 mmol) and sodium hypophosphite hydrate (36.0 g, 340 mmol) were added sequentially. The reaction mixture was heated and stirred at reflux for about 3 hours. After completion of the reaction, it was cooled to room temperature, filtered, the solid was washed with water and methanol, and dried under vacuum to give the light yellow target compound 109 (2-bromo-9,10-bis(2-naphthyl)anthracene, 10.1 g, 96% yield).

References

[1] Patent: US7485733, 2009, B2. Location in patent: Page/Page column 76
[2] Patent: WO2003/95445, 2003, A1. Location in patent: Page/Page column 72
[3] Patent: EP1465874, 2004, A2. Location in patent: Paragraph 0051
[4] Patent: EP1465874, 2013, B1. Location in patent: Paragraph 0051
[5] Patent: US6998487, 2006, B2. Location in patent: Page/Page column 51

2-Bromo-9,10-bis(2-naphthalenyl)anthracene Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 2-Bromo-9,10-bis(2-naphthalenyl)anthracene manufacturers

Henan Aochuang Chemical Co.,Ltd.
Product
2-Bromo-9,10-bis(2-naphthalenyl)anthracene 474688-76-1
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1ton
Release date
2022-09-27
Shanghai Daken Advanced Materials Co.,Ltd
Product
2-Bromo-9,10-di-2-phthalenylanthracene 474688-76-1
Price
US $0.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
150KG /month
Release date
2021-11-19
Henan Fengda Chemical Co., Ltd
Product
2-Bromo-9,10-bis(2-naphthalenyl)anthracene 474688-76-1
Price
US $188.00-1.00/KG
Min. Order
1KG
Purity
99%, 99.5% Sublimated
Supply Ability
g-kg-tons, free sample is available
Release date
2024-01-05

474688-76-1, 2-Bromo-9,10-bis(2-naphthalenyl)anthraceneRelated Search:


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