9-Bromo-10-phenylanthracene

9-Bromo-10-phenylanthracene

9-Bromo-10-phenylanthracene

CAS: 23674-20-6

Molecular Formula: C20H13Br

9-Bromo-10-phenylanthracene - Names and Identifiers

Name	9-Bromo-10-phenylanthracene
Synonyms	9-Bromo-10-phenyl 9-Bromo-10-phenylant 9-bromo-10-phenylindole 10-broMo-9-phenylanthracene 10-phenyl-9-BroMoanthracene 10-phenyl-9-Bromoanthracene 9-Bromo-10-phenylanthracene 9-bromo-10-phenylanthrancene Anthracene, 9-Bromo-10-phenyl anthracene, 9-bromo-10-phenyl-
CAS	23674-20-6
EINECS	621-755-8
InChI	InChI=1/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

9-Bromo-10-phenylanthracene - Physico-chemical Properties

Molecular Formula	C20H13Br
Molar Mass	333.22
Density	1.393
Melting Point	154-155 °C
Boling Point	449.7±14.0 °C(Predicted)
Flash Point	221.3°C
Water Solubility	Insoluble in water. Soluble in hot toluene, dimethylformamide.
Solubility	Chloroform, Methanol (Slightly)
Vapor Presure	7.45E-08mmHg at 25°C
Appearance	Powder
Color	Pale yellow
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.717
MDL	MFCD00230983

9-Bromo-10-phenylanthracene - Risk and Safety

Safety Description	24/25 - Avoid contact with skin and eyes.
HS Code	29039990

9-Bromo-10-phenylanthracene - Reference Information

introduction	9-bromo-10-phenylanthracene, English name 9-Bromo-10-phenylanthracene, yellow-white solid powder under normal temperature and pressure, is a common organic synthesis intermediate.
solubility	9-bromo-10-phenylanthracene is insoluble in water, but soluble in dimethyl sulfoxide, N,N-dimethylformamide, etc. It is worth noting that due to the small polarity of the compound, according to the principle of similar phase solubility, the compound can be dissolved in a hot non-polar solvent, such as toluene.
Use	9-bromo-10-phenylanthracene, as an organic synthesis intermediate, due to its unique The structure of the polyaromatic ring makes it widely used in fluorescent molecular dyes and organic luminescent materials. Experimentalists often increase the conjugate system of the molecule by introducing the phenyl anthracene structure, which increases the delocalization range of electrons, giving the molecule unique optical and chemical properties. As an organic synthetic block, bromine atoms can be converted into boric acid, aryl, alkyl, etc. through functional group conversion.
synthesis method	9-bromo-10-phenylanthracene is 9,10-dibromo anthracene as the starting material, obtained by one Suzuki coupling with phenylboronic acid. However, the obvious disadvantage of this route is that the reaction may get the by-product of the coupling twice, and the by-product of the coupling twice and the unreacted raw material and the target product are similar in polarity, resulting in difficulty in separation. Therefore, when using this method, special attention should be paid to the equivalence ratio of the reaction and the monitoring of the reaction progress.
preservation method	9-bromo-10-phenylanthracene should be stored in a cool place, and the storage place must be kept away from oxidant. Current data show that the compound has stable chemical properties and is not easy to deteriorate, and there is no report on its special reactivity.

Last Update：2024-04-10 22:29:15

9-Bromo-10-phenylanthracene

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Shanghai Yuanye Bio-Technology Co., Ltd.

Product Name: 9-Bromo-10-phenyl-anthracene Visit Supplier Webpage Request for quotation
CAS: 23674-20-6
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409

Click to send a QQ message

Wechat: 18301782025

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9-Bromo-10-phenylanthracene

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