1687-94-1

Basic information

• Product Name: 5,10-diphenylindeno[2,1-a]indene
• CAS NO: 1687-94-1
• Molecular Formula: C₂₈H₁₈
• Molecular Weight: 354.4425
• Mol File: 1687-94-1.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 531.2°C at 760 mmHg
• Flash Point: 272.7°C
• Density: 1.25g/cm³
• Vapor Pressure: 7.84E-11mmHg at 25°C
• Refractive Index: 1.744
• CAS DataBase Reference: 5,10-diphenylindeno[2,1-a]indene(CAS DataBase Reference)
• NIST Chemistry Reference: 5,10-diphenylindeno[2,1-a]indene(1687-94-1)
• EPA Substance Registry System: 5,10-diphenylindeno[2,1-a]indene(1687-94-1)

Safety Data

• Hazardous Substances Data: 1687-94-1(Hazardous Substances Data)

Upstream product

• 123765-11-7 5,10-diphenyl-4b,5,9b,10-tetrahydro-indeno[2,1-a]indene-5,10-diol 
• 108020-68-4 1.1-Dibrom-tetraphenyltellurophen 
• 23116-48-5 5-Chloro-10-phenylindeno<2,1-a>indene 
• 591-51-5 phenyllithium 
• 91861-63-1 5,6,11,12-Tetrabromdibenzocycloocten 
• 67761-47-1 (5Z,11Z)-5,11-diphenyldibenzo[a,e][8]annulene 
• 1608-10-2 1,2,3,4-tetraphenyl-1,3-butadiene 
• 50703-54-3 4b,9b-dihydro-indeno[2,1-a]indene-5,10-dione 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 13203-60-6 1,2-bis(2-phenylethynyl)benzene 
• 17261-24-4 5-phenylindeno<2,1-a>indene 
• 21375-88-2 1-bromo-2-(phenylethenyl)benzene 
• 1043009-23-9 bis[o-(phenylcarbonyl)phenyl]acetylene 
• 1123215-48-4 C₃₀H₄₄Sn 

Downstream Products

• 91861-68-6 5,10-diphenyl-5,10-dihydro-indeno[2,1-a]indene 
• 85-52-9 2-Benzoylbenzoic acid 
• 861305-11-5 2,2'-Dibenzoyl-benzil 

Relevant articles and documents

Facile synthesis of a pyrrole-fused dibenzo[a,e]pentalene and its application as a new extended, ladder-type fused aromatic system

A novel ladder-type pyrrole-fused dibenzo[a,e]pentalene, in which two benzo[a,e]pentalene units are held coplanar by a nitrogen bridge, is synthesized via double intermolecular Pd-catalyzed cascade crossover annulations. The introduction of a nitrogen bridge not only has a substantial influence on the optoelectronic properties but also improves the processability and stability. This journal is

Increased Antiaromaticity through Pentalene Connection in [ n]Cyclo-1,5-dibenzopentalenes

Conjugated nanohoops incorporating nonalternant hydrocarbons have altered optoelectronic properties compared to [n]cycloparaphenylenes or other purely aromatic hoops. We synthesized [n]cyclo-1,5-dibenzopentalenes (n = 4, 5), in which nonalternant dibenzo[a,e]pentalenes are connected through their pentalene units. This leads to an increase in antiaromatic character and low-lying LUMO energies. Calculations show puckered or entangled conformations of the precursor macrocyclic Pt-complexes. Our study proves dibenzopentalene as a versatile nonalternant building block for conjugated nanohoops with modifiable antiaromaticity and optoelectronic properties.

MULTICYCLIC AROMATIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME

The present specification describes a multicyclic aromatic ring compound having a novel structure and an organic light emitting device using the same.