324750-99-4

Basic information

• Product Name: 9,10-Bis(4-formylphenyl)anthracene
• Synonyms: 9,10-Bis(4-formylphenyl)anthracene
• CAS NO: 324750-99-4
• Molecular Formula: C₂₈H₁₈O₂
• Molecular Weight: 386.44
• Mol File: 324750-99-4.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 9,10-Bis(4-formylphenyl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9,10-Bis(4-formylphenyl)anthracene(324750-99-4)
• EPA Substance Registry System: 9,10-Bis(4-formylphenyl)anthracene(324750-99-4)

Safety Data

• Hazardous Substances Data: 324750-99-4(Hazardous Substances Data)

Usage

General Description

9,10-Bis(4-formylphenyl)anthracene is a chemical compound with the molecular formula C30H20O2. It is a derivative of anthracene, consisting of a central anthracene backbone with two formylphenyl groups attached at the 9 and 10 positions. 9,10-Bis(4-formylphenyl)anthracene is used in organic synthesis and materials science for its potential as a building block for the development of new organic materials and fluorescent compounds. It has been studied for its photophysical properties and potential applications in optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics. Additionally, it has been investigated for its potential use in generating singlet oxygen in photodynamic therapy for cancer treatment.

Upstream product

• 95952-57-1 9,10-bis-(4-chloro-phenyl)-anthracene 
• 68-12-2 N,N-dimethyl-formamide 
• 1679-18-1 4-Chlorophenylboronic acid 
• 523-27-3 9,10-Dibromoanthracene 
• 863992-56-7 9,10-bis(4,4,5,5,-tetramethyl[1.3.2]dioxaborolan-2-yl)anthracene 
• 1122-91-4 4-bromo-benzaldehyde 
• 87199-17-5 4-formylphenylboronic acid, 

Downstream Products

• 324751-03-3 9,10-bis[4-(4,4,5,5-tetramethyl-1,3-dihydroxyimidazolidin-2-yl)phenyl]anthracene 
• 1252813-34-5 9,10-bis(4-((3,5-dicyano-2,6-dipyrid-4-yl)dihydropyrid-4-yl)phenyl)anthracene 

Relevant articles and documents

Luminescence Ratiometric Nanothermometry Regulated by Tailoring Annihilators of Triplet–Triplet Annihilation Upconversion Nanomicelles

Triplet–triplet annihilation (TTA) upconversion is a special non-linear photophysical process that converts low-energy photons into high-energy photons based on sensitizer/annihilator pairs. Here, we constructed a novel luminescence ratiometric nanothermo

Efficient synthesis of organic semiconductors by Suzuki-Miyaura coupling in an aromatic micellar medium

Micellar catalysis enables carrying out Suzuki-Miyaura couplings in water under exceptionally mild conditions. Extension of such a protocol to the sustainable synthesis of highly conjugated, poorly soluble materials like [1]benzothieno[3,2-b][1]benzothiop

Organic light-emitting material with anthracene structure and organic light-emitting device with anthracene structure

The invention provides an organic light-emitting material with anthracene structure and an organic light-emitting device with anthracene structure and belongs to the technical field of organic photoelectric materials. The organic light-emitting material with anthracene structure comprises anthracene rings that are a blue light-emitting material parent nucleus structure having excellent performanceand having high triplet state energy level and wide energy gap; by connecting benzimidazole groups to molecules, the material is provided with improved electron transport capacity so that carrier transport is balanced. Compared with the prior art, the organic light-emitting material with anthracene structure applied to organic light-emitting devices, particularly as blue objective material in a light-emitting layer has higher luminous efficiency.