3-Bromo-7,12-diphenylbenzo[k]fluoranthene

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Company Name: Springchem New Material Technology Co.,Limited
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Products Intro: Product Name:3-Bromo-7,12-diphenylbenzo[k]fluoranthene
CAS:187086-32-4
Purity:0.99 Package:25kg;5KG;1KG Remarks:R
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Products Intro: Product Name:3-Bromo-7,12-diphenylbenzo[k]fluoranthene
CAS:187086-32-4
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Company Name: Beijing Green Guardee Technology Co., Ltd
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Products Intro: Product Name:3-Bromo-7,12-diphenylbenzo[k]fluoranthene
CAS:187086-32-4
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Products Intro: Product Name:3-Bromo-7,12-diphenylbenzo[k]fluoranthene
CAS:187086-32-4
Purity:99% Package:1KG;1USD
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CAS:187086-32-4
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3-Bromo-7,12-diphenylbenzo[k]fluoranthene manufacturers

3-Bromo-7,12-diphenylbenzo[k]fluoranthene Basic information
Product Name:3-Bromo-7,12-diphenylbenzo[k]fluoranthene
Synonyms:3-Bromo-7,12-diphenylbenzo[k]fluoranthene;Benzo[k]fluoranthene, 3-bromo-7,12-diphenyl;3-Bromo-7,12-diphenylbenzo[k]fluoranthrene
CAS:187086-32-4
MF:C32H19Br
MW:483.4
EINECS:
Product Categories:
Mol File:187086-32-4.mol
3-Bromo-7,12-diphenylbenzo[k]fluoranthene Structure
3-Bromo-7,12-diphenylbenzo[k]fluoranthene Chemical Properties
Boiling point 649.4±24.0 °C(Predicted)
density 1.409
storage temp. Sealed in dry,Room Temperature
form solid
InChI1S/C32H19Br/c33-27-19-18-26-30-24(27)16-9-17-25(30)31-28(20-10-3-1-4-11-20)22-14-7-8-15-23(22)29(32(26)31)21-12-5-2-6-13-21/h1-19H
InChIKeyMBWSEPXTVAGLJS-UHFFFAOYSA-N
SMILESBrC(C=C1)=C2C3=C1C4=C(C5=CC=CC=C5)C6=CC=CC=C6C(C7=CC=CC=C7)=C4C3=CC=C2
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
3-Bromo-7,12-diphenylbenzo[k]fluoranthene Usage And Synthesis
Synthesis
7,12-diphenylbenzo[k]fluoranthene

16391-62-1

3-Bromo-7,12-diphenylbenzo[k]fluoranthene

187086-32-4

Example 1. Synthesis of 3-bromo-7,12-diphenylbenzo[k]fluoranthene To a solvent mixture of 50 mL of N-methylpyrrolidone (NMP) and 500 mL of dichloromethane were added 10.0 g (25 mmol) of 7,12-diphenylbenzo[k]fluoranthene (see WO2010/031833 for preparation) and 6.45 g (36 mmol) of N-bromosuccinimide (NBS). The reaction mixture was stirred at room temperature for 20 hours. Upon completion of the reaction, the dichloromethane was evaporated under reduced pressure and the product was subsequently precipitated by addition of water. The precipitate was collected by filtration and dried to give 12.1 g (quantitative yield) of the title compound as a beige solid. Thin layer chromatography (TLC) analysis showed an Rf value of 0.9 (unfolding agent ratio petroleum ether:toluene = 2:1).

References[1] Patent: WO2012/123888, 2012, A1. Location in patent: Page/Page column 60-61
[2] Patent: US2016/284947, 2016, A1. Location in patent: Paragraph 0296; 0297; 0298
[3] Patent: CN107778199, 2018, A. Location in patent: Paragraph 0060; 0066; 0072
[4] Patent: EP2907803, 2015, A1. Location in patent: Page/Page column 137
[5] Patent: TWI558705, 2016, B. Location in patent: Paragraph 0140; 0147
3-Bromo-7,12-diphenylbenzo[k]fluoranthene Preparation Products And Raw materials
Raw materials5-Bromo Acenaphthylene-->7,12-diphenylbenzo[k]fluoranthene-->1,3-Diphenylisobenzofuran-->Dichloromethane-->N-Bromosuccinimide-->N-Methyl-2-pyrrolidone
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