7059-70-3

Basic information

• Product Name: 1,3,5-Tri(1-naphthyl)benzene
• Synonyms: 1,3,5-Tri(1-naphthyl)benzene;2-(3,5-dinaphthalen-2-ylphenyl)naphthalene
• CAS NO: 7059-70-3
• Molecular Formula: C36H24
• Molecular Weight: 456.57576
• EINECS: -0
• Mol File: 7059-70-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 184.0 to 188.0 °C
• Boiling Point: 626.6±50.0 °C(Predicted)
• Appearance: /
• Density: 1.177±0.06 g/cm3(Predicted)
• Storage Temp.: Room Temperature, under inert atmosphere
• Solubility: Chloroform (Sparingly), DMSO (Slightly)
• CAS DataBase Reference: 1,3,5-Tri(1-naphthyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Tri(1-naphthyl)benzene(7059-70-3)
• EPA Substance Registry System: 1,3,5-Tri(1-naphthyl)benzene(7059-70-3)

Safety Data

• Hazardous Substances Data: 7059-70-3(Hazardous Substances Data)

Usage

Chemical structure

1,3,5-Tri(1-naphthyl)benzene consists of three naphthyl groups attached to a benzene ring.

Usage

Mainly used as a building block in organic synthesis and as a precursor in the production of organic electronic materials.

Organic light-emitting diodes (OLEDs)

Used in the development of OLEDs due to its strong blue fluorescence.

Organic semiconductors

Used in the production of organic semiconductors.

Thermal stability

Known for its high thermal stability.

Fluorescence

Emits strong blue fluorescence, making it useful in the development of advanced optoelectronic devices.

Material science

Has potential applications in the field of material science, particularly in the development of high-performance organic materials for various technological applications.

Upstream product

• 66-77-3 1-naphthaldehyde 
• 37630-26-5 β-(1-naphthyl)nitroethylene 
• 626-39-1 1,3,5-trisbromobenzene 
• 13922-41-3 1-Naphthylboronic acid 
• 15727-65-8 1-ethynylnaphthalene 
• 941-98-0 1'-naphthacetophenone 
• 142-04-1 aniline hydrochloride 

Relevant articles and documents

Triple condensation of aryl methyl ketones catalyzed by amine and trifluoroacetic acid: Straightforward access to 1,3,5-triarylbenzenes under mild conditions

An efficient triple condensation reaction of aryl methyl ketones catalyzed by ethylenediamine and trifluoroacetic acid was reported. A broad scope of 1,3,5-triarylbenzenes was obtained in good to excellent yields. The reaction provides a novel and practical approach to access organic materials of polycyclic aromatic hydrocarbons under mild conditions.

Highly selective biaryl formation by the cyclooligomerization of arylethynes catalyzed by rhodium and ruthenium porphyrins

Rhodium and ruthenium porphyrins catalyze the one-pot formation of biaryl derivatives from arylethynes with high selectivity, giving interesting derivatives not easy to obtain using other different methods; the porphyrin catalysts can be recovered and reu