1123921-69-6

Basic information

• Product Name: 2-iodo-9,10-diphenylanthracene
• Synonyms: 2-iodo-9,10-diphenylanthracene
• CAS NO: 1123921-69-6
• Molecular Weight: 456.325
• Mol File: 1123921-69-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-iodo-9,10-diphenylanthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-iodo-9,10-diphenylanthracene(1123921-69-6)
• EPA Substance Registry System: 2-iodo-9,10-diphenylanthracene(1123921-69-6)

Safety Data

• Hazardous Substances Data: 1123921-69-6(Hazardous Substances Data)

Upstream product

• 117-79-3 2-aminoanthraquinone 
• 572-83-8 2-bromoanthracene-9,10-dione 
• 860530-98-9 2-bromo-9,10-diphenyl-9,10-dihydro-anthracene-9,10-diol 

Downstream Products

• 1123921-74-3 2-(3-bromophenyl)-9,10-diphenylanthracene 
• 1123921-68-5 2-(4-bromophenyl)-9,10-diphenylanthracene 
• 1307859-78-4 4-[3-(9,10-diphenyl-2-anthryl)phenyl]-2,8-diphenyldibenzofuran 
• 1365891-54-8 3-(dibenzothiophen-4-yl)-9-(9,10-diphenyl-2-anthryl)-9H-carbazole 
• 1123921-70-9 2-{4-[N-(4-diphenylaminophenyl)-N-phenylamino]phenyl}-9,10-diphenylanthracene 
• 1123921-71-0 2-[4-[N-phenyl-N-(9-phenylcarbazol-3-yl)amino]phenyl]-9,10-diphenylanthracene 
• 1136225-77-8 2-(4-{N-[4-(carbazol-9-yl)phenyl]-N-phenylamino}phenyl)-9,10-diphenylanthracene 
• 1123921-73-2 2-{3-[N-phenyl-N-(9-phenylcarbazol-3-yl)amino]phenyl}-9,10-diphenylanthracene 
• 1123921-75-4 2-(3-{N-[4-(carbazol-9-yl)phenyl]-N-phenylamino}phenyl)-9,10-diphenylanthracene 
• 1404222-73-6 N-[4-(9,10-diphenyl-2-anthryl)phenyl]-N,N',N'-triphenylbenzidine 
• 1404222-74-7 4-[4-(9H-carbazol-9-yl)phenyl]-4'-(9,10-diphenyl-2-anthryl)triphenylamine 

Relevant articles and documents

Synthesis of 9,10-Diarylanthracenes via Mg(TMP) 2 ·2LiCl-Mediated Benzyne Generation/[4+2] Cycloaddition and Deoxygenation of 9,10-Epoxyanthracene Intermediates

A new synthetic route to functionalized 9,10-diarylanthracenes has been developed. 9,10-Epoxyanthracene intermediates were prepared by [4+2] cycloaddition of 1,3-diarylisobenzofuran with a variety of functionalized benzyne intermediates, which were obtained by Mg(TMP) 2 ·2LiCl-mediated benzyne generation. For the cleavage of the resultant 9,10-epoxyanthracene intermediates, we developed mild deoxygenation conditions using a combination of trifluoroacetic acid and Et 3 SiH. The utility of this sequence was demonstrated by application to the synthesis of 5,7,12,14-tetraphenylpentacene.