2,6-Dibromoanthraquinone CAS 633-70-5

Introduction:Basic information about 2,6-Dibromoanthraquinone CAS 633-70-5, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

2,6-Dibromoanthraquinone Basic information

Product Name:2,6-Dibromoanthraquinone
Synonyms:2,6-DIBROMOANTHRAQUINONE;9,10-Anthracenedione,2,6-dibroMo-;2,6-Dibromonathraquinone;2,6-Dibromoanthraqui;2,6-Dibromoanthracene-9,10-dione;2,6-dibroMo-9,10-dihydroanthracene-9,10-dione;9,10-Anthracenedione, 2,6-dibroMo-2,6-DibroMoanthracene-9,10-dione;2,6-Dibromoanthracene-9,1-dione
CAS:633-70-5
MF:C14H6Br2O2
MW:366
EINECS:1592732-453-0
Product Categories:Anthracene derivatives;Electronic Chemicals;Anthraquinones;Chloroanthraquine, etc.;Anthracene series
Mol File:633-70-5.mol

2,6-Dibromoanthraquinone Chemical Properties

Melting point 290 °C
Boiling point 491.8±45.0 °C(Predicted)
density 1.911±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
color Light yellow to Brown

Safety Information

HS Code 2914.69.9000

2,6-Dibromoanthraquinone Usage And Synthesis

Uses2,6-Dibromoanthraquinone is an organic raw material that can be widely used in the preparation of organic light-emitting materials.
Chemical PropertiesYellow crystalline powder
Synthesis

131-14-6

633-70-5

Synthesis Example 2: Synthesis of Compound 82-1) Synthesis of 2,6-dibromoanthraquinoneIn a 10L flask, 198.2 g (1.5 mol) of tert-butyl nitrite and 279.1 g (1.2 mol) of copper (II) bromide were dissolved in 6000 ml of acetonitrile. After raising the temperature of the reaction system to 65 °C, 119.1 g (0.5 mol) of 2,6-diaminoanthraquinone was slowly added and the addition process lasted for 5 min. After the nitrogen generation stopped, the reaction mixture was cooled to room temperature. Subsequently, 3.6 L of aqueous 2N hydrochloric acid was added to the reaction mixture and stirred until the solid precipitated. The solid product was collected by filtration, washed sequentially with excess water, methanol and acetone, and dried to give 2,6-dibromoanthraquinone (180 g, 98.4% yield).

References[1] Patent: EP2292604, 2011, A2. Location in patent: Page/Page column 23
[2] Angewandte Chemie - International Edition, 2018,
[3] Angew. Chem., 2018, vol. 130, # 48, p. 15907 - 15911,5
[4] Tetrahedron, 2014, vol. 70, # 2, p. 262 - 269
[5] Tetrahedron, 2017, vol. 73, # 40, p. 5892 - 5899

2,6-Dibromoanthraquinone Preparation Products And Raw materials

Raw materialsAnthracene, 2,6,9,10-tetrabromo--->Benzoic acid, 4-broMo-2-(4-broMobenzoyl)-4-BroMo-2-(p-broMobenzoyl)benzoic acid-->2,6-Diaminoanthraquinone-->Acetonitrile-->Cupric bromide-->Ethanol-->tert-Butyl nitrite-->Acetic acid
Preparation Products2,6-Dibromo-9,10-di(naphthalen-1-yl)anthracene-->2,6-DIBROMOANTHRACENE
2,6-DIBROMOANISOLE CAS 38603-09-7
2,6-DICHLORO-4-(TRIFLUOROMETHYL)PHENYLHYDRAZINE CAS 86398-94-9
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