151721-78-7

Basic information

• Product Name: Benzene, 1,3,5-tribromo-2,4,6-triiodo-
• CAS NO: 151721-78-7
• Molecular Formula: C6Br3I3
• Molecular Weight: 692.492
• Mol File: 151721-78-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, 1,3,5-tribromo-2,4,6-triiodo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,3,5-tribromo-2,4,6-triiodo-(151721-78-7)
• EPA Substance Registry System: Benzene, 1,3,5-tribromo-2,4,6-triiodo-(151721-78-7)

Safety Data

• Hazardous Substances Data: 151721-78-7(Hazardous Substances Data)

Upstream product

• 626-39-1 1,3,5-trisbromobenzene 
• 626-44-8 1,3,5-Triiodobenzene 

Downstream Products

• 298-12-4 Glyoxilic acid 
• 1206891-68-0 1,3,5-tribromo-2,4,6-tris[4-( p-dioctylaminostyryl)phenylethynyl]benzene 
• 1206891-69-1 1,3-dibromo-2,4,5,6-tetrakis[4-( p-dioctylaminostyryl)phenylethynyl]benzene 
• 1206891-70-4 1-bromo-2,3,4,5,6-pentakis[4-( p-dioctylaminostyryl)phenylethynyl]benzene 
• 684216-84-0 1,3,5-tris[p-(tert-butyldimethylsilyloxy)phenylethynyl]-2,4,6-tris[p-(ethoxycarbonyl)phenylethynyl]benzene 
• 684216-74-8 1,3,5-tribromo-2,4,6-tris[p-(N,N-di-n-octylamino)phenylethynyl]benzene 
• 684216-75-9 1,3-dibromo-2,4,5,6-tetrakis[p-(N,N-di-n-octylamino)phenylethynyl]benzene 
• 684216-71-5 1,3,5-tribromo-2,4,6-tris[p-(tert-butyldimethylsilyloxy)phenylethynyl]benzene 
• 684216-73-7 1-bromo-2,3,4,5,6-pentakis[p-(tert-butyldimethylsilyloxy)phenylethynyl]benzene 

Relevant articles and documents

Organic Thin-film Solar Cells Using Benzotrithiophene Derivatives Bearing Acceptor Units as Non-Fullerene Acceptors

New star-shaped non-fullerene acceptors (5Z,5′Z,5′′Z)-5,5′,5′′-((benzo[1,2-b : 3,4-b′ : 5,6-b′′]trithiophene-2,5,8-triyltris(4-octylthiophene-5,2-diyl))tris(methaneylylidene))tris(3-octyl-2-thioxothiazolidin-4-one) (1: BTT-OT-ORD) and 2,2′,2′′-((5Z,5′Z,5′′Z)-((benzo[1,2-b : 3,4-b′ : 5,6-b′′]trithiophene-2,5,8-triyltris(4-octylthiophene-5,2-diyl))tris(methaneylylidene))tris(3-octyl-4-oxothiazolidine-5,2-diylidene))trimalononitrile (2: BTT-OT-OTZDM) with a benzotrithiophene core, alkyl-thiophen units, and acceptor units were designed and synthesized. The HOMO-LUMO levels of 1 and 2 were determined by photoemission spectroscopy and UV-Vis absorption spectroscopy. Binary blend and ternary blend bulk heterojunction (BHJ) organic solar cells with non-fullerene acceptors 1 and 2 were fabricated with the inverted device structures of glass/ITO/ZnO/active_layer/MoO3/Ag. Both binary blend BHJ solar cells with 1 and 2 show lower JSC and larger VOC values than P3HT : PCBM solar cells. On the other hand, ternary blend BHJ organic solar cells, including 10 % of 1, exhibited a larger power conversion efficiency than P3HT : PCBM solar cells because the JSC value was largely improved.

Isostructurality, polymorphism and mechanical properties of some hexahalogenated benzenes: The nature of halogen...halogen interactions

The nature of intermolecular interactions between halogen atoms, X...X (X = Cl, Br, I), continues to be of topical interest because these interactions may be used as design elements in crystal engineering. Hexahalogenated benzenes (C6Cl6-n

Polyiodination on benzene at room temperature. A regioselective synthesis of derivatives

Reaction of IPy2BF4 with benzene and CF3SO3H in CH2Cl2 gives regioselectively polyiodinated compounds at room temperature, providing a definitely easy synthetic entry to those rarely accessible benzene derivatives.