1196107-73-9
1196107-73-9 Basic information
- Product Name:
- 1196107-73-9
- Synonyms:
-
- 2-Bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dione
- 2-BroMo-13,13-diMethyl-13H 22 -indeno[1,2-b]anthracene-6,1 1-dione
- 2-bromo-13,13-dimethyl- 6H-Indeno[1,2-b]anthracene-6,11(13H)-dio
- 2-Bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dione
- 2-bromo-13,13-dimethyl- 6H-Indeno[1,2-b]anthracene-6,1
- 2-Bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dione>
- 6H-Indeno[1,2-b]anthracene-6,11(13H)-dione, 2-bromo-13,13-dimethyl-
- 1196107-73-9 ISO 9001:2015 REACH
- CAS:
- 1196107-73-9
- MF:
- C23H15BrO2
- MW:
- 403.27
- Mol File:
- 1196107-73-9.mol
1196107-73-9 Chemical Properties
- Melting point:
- 264 °C
- Boiling point:
- 570.7±49.0 °C(Predicted)
- Density
- 1.479
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to crystal
- color
- Light yellow to Yellow to Orange
- CAS DataBase Reference
- 1196107-73-9
1196107-73-9 Usage And Synthesis
Chemical Properties
Yellow solid
Synthesis
1196107-72-8
1196107-73-9
General procedure: 2-Bromo-9,9-dimethyl-7-(2-carboxybenzoyl)fluorene (20 g, 0.047 mol, 1 eq.) was used as a raw material, which was placed in a reaction flask and polyphosphoric acid (50 ml) was added. The reaction mixture was heated to 140 °C for the reaction. After completion of the reaction, the resulting solid product was filtered, washed with a small amount of methanol and then dried to afford the target compound 2-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dione (16.6 g, 81% yield). The product was characterized by 1H-NMR: δ 8.29 (t, 2H), 8.09 (s, 2H), 7.85 (d, 2H), 7.72 (m, 3H), 1.67 (s, 6H).
References
[1] Patent: US2011/57182, 2011, A1
[2] Patent: US2012/161615, 2012, A1
[3] Patent: JP5781506, 2015, B2. Location in patent: Paragraph 0165-0167
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