171368-81-3

Basic information

• Product Name: Benzene, 1-bromo-2,5-bis(dodecyloxy)-4-nitro-
• CAS NO: 171368-81-3
• Molecular Formula: C30H52BrNO4
• Molecular Weight: 570.651
• Mol File: 171368-81-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1-bromo-2,5-bis(dodecyloxy)-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-bromo-2,5-bis(dodecyloxy)-4-nitro-(171368-81-3)
• EPA Substance Registry System: Benzene, 1-bromo-2,5-bis(dodecyloxy)-4-nitro-(171368-81-3)

Safety Data

• Hazardous Substances Data: 171368-81-3(Hazardous Substances Data)

Upstream product

• 171368-73-3 2,5-bis(dodecyloxy)bromobenzene 
• 123-31-9 hydroquinone 
• 3230-09-9 1,4-bis-dodecyloxy-benzene 
• 143-15-7 1-dodecylbromide 
• 583-69-7 2-bromobenzene-1,4-diol 

Downstream Products

• 523978-90-7 1,4-bis(dodecyloxy)-2-[(trimethylsilyl)ethynyl]-5-iodobenzene 
• 870080-50-5 4-[4-{[(2'-(2'',5''-bis(dodecyloxy)-4''-(2'-trimethylsilylethynyl)phenyl)]ethynyl}-2,5-bis(dodecyloxy)phenyl)ethynyl]benzaldehyde 
• 870080-47-0 4-{[2'-(2'',5''-bis(dodecyloxy)-4''-(2'-trimethylsilylethynyl)phenyl)]ethynyl}-2,5-bis(dodecyloxy)iodobenzene 
• 870080-48-1 4-{[2'-(2'',5''-bis(dodecyloxy)-4''-(2'-trimethylsilylethynyl)phenyl)]ethynyl}benzaldehyde 

Relevant articles and documents

Synthesis and Properties of Triphenodioxazine-Based Conjugated Polymers for Polymer Solar Cells

As a fused-ring conjugated unit, triphenodioxazine, has been applied in two series of thiophene-free conjugated polymers for polymer solar cells. The polymers were synthesized through a multi-step synthetic route, and the substituents had a great effect on the reactivity of the reactants. Relationships among the polymer structures as well as thermal, optical, and electrochemical properties were investigated in detail by experimental data analysis and theoretical simulation. The polymers possess highly planar backbones, broad Vis/NIR absorption bands, suitable frontier molecular orbital energies, and low band gaps ranging from 1.3 to 1.8 eV. The power conversion efficiencies of their photovoltaic devices are about 1 %. Introducing longer alkyl side chains into a polymer can bring about a better film-forming ability and improve the photovoltaic performance.

Distance-independent photoinduced energy transfer over 1.1 to 2.3 nm in ruthenium trisbipyridine-fullerene assemblies

Ruthenium trisbipyridine C60 dyads linked via para-phenyleneethynylene units have been prepared. They displayed a rapid energy transfer from Ru to C60 with a rate that was independent of distance, from 1.1 to 2.3 nm. The results are