848153-57-1

Basic information

• Product Name: Benzenamine, 4,4'-(1E)-1,2-ethenediylbis[N,N-bis(4-methoxyphenyl)-
• CAS NO: 848153-57-1
• Molecular Formula: C42H38N2O4
• Molecular Weight: 634.775
• Mol File: 848153-57-1.mol

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4,4'-(1E)-1,2-ethenediylbis[N,N-bis(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4,4'-(1E)-1,2-ethenediylbis[N,N-bis(4-methoxyphenyl)-(848153-57-1)
• EPA Substance Registry System: Benzenamine, 4,4'-(1E)-1,2-ethenediylbis[N,N-bis(4-methoxyphenyl)-(848153-57-1)

Safety Data

• Hazardous Substances Data: 848153-57-1(Hazardous Substances Data)

Upstream product

• 18869-30-2 (E)-4,4'-dibromostilbene 
• 101-70-2 bis(4-methoxyphenyl)amine 
• 89115-20-8 4-[bis(4-methoxyphenyl)amino]benzaldehyde 
• 104-94-9 4-methoxy-aniline 
• 2039-86-3 3-bromostyrene 
• 589-87-7 1,4-bromoiodobenzene 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 1122-91-4 4-bromo-benzaldehyde 
• 38186-51-5 diethyl (4-bromobenzyl)phosphonate 
• 106948-30-5 (E)-2-(3-bromophenyl)-1-(4-bromophenyl)ethene 

Relevant articles and documents

Efficient Hole Transporting Materials with Two or Four N,N-Di(4-methoxyphenyl)aminophenyl Arms on an Ethene Unit for Perovskite Solar Cells

Novel steric bulky hole transporting materials (HTMs) with two or four N,N-di(4-methoxyphenyl)aminophenyl units have been synthesized. When the EtheneTTPA was used as a hole transporting material in perovskite solar cell, the power conversion efficiency a

A mixed-valence bis(diarylamino)stilbene: Crystal structure and comparison of electronic coupling with biphenyl and tolane analogues

The E-4,4′-bis[di(p-anisyl)amino]stilbene cation is a class-III mixed-valence species with electronic coupling comparable to that in its biphenyl-bridged analogue, whereas its tolane-bridged analogue belongs to class II. The Royal Society of Chemistry 200

Intervalence transitions in the mixed-valence monocations of bis(triarylamines) linked with vinylene and phenylene-vinylene bridges

(E)-4,4′-Bis{bis(4-methoxyphenyl)amino}stilbene, 1, (E,E)-1,4-bis[4-{bis(4-methoxyphenyl)-amino}styryl]benzene, 2, and two longer homologues, (E,E,E)-4,4′-bis[4-{bis(4-methoxyphenyl)amino}-styryl] stilbene, 3, and (E,E,E,E)-1,4-bis(4-[4-{bis(4-methoxyphen

3,4'-Bis[bis(t-butyl- and methoxy-phenyl)amino]stilbene bis(cation radical)s and their electrochemical and magnetic properties

3,4'-Bis[bis(p-t-butylphenyl)amino]stilbene 1a and 3,4'-bis[bis(p- methoxyphenyl)amino]stilbene 1b were synthesized. The oxidation of 1 was analyzed by electrochemical measurements, which revealed the reversible formation of the bis(cation radical) 2 via a two-electron transfer reaction. The chemical oxidation of 1 with NOBF4 also gave the bis(cation radical) 2; UV/vis and ESR spectroscopies supported aminium radical formation without any side reaction. Magnetization, magnetic susceptibility, and the ESR ΔM(s) = ±2 signal of the biradicals indicated triplet ground states with a large triplet-singlet energy gap.