1365548-84-0

Basic information

• Product Name: 10-bromo-7-(4-phenylquinazolin-2-yl)-7H-benzo[c]carbazole
• Synonyms: 10-bromo-7-(4-phenylquinazolin-2-yl)-7H-benzo[c]carbazole
• CAS NO: 1365548-84-0
• Molecular Weight: 500.397
• Mol File: 1365548-84-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 10-bromo-7-(4-phenylquinazolin-2-yl)-7H-benzo[c]carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 10-bromo-7-(4-phenylquinazolin-2-yl)-7H-benzo[c]carbazole(1365548-84-0)
• EPA Substance Registry System: 10-bromo-7-(4-phenylquinazolin-2-yl)-7H-benzo[c]carbazole(1365548-84-0)

Safety Data

• Hazardous Substances Data: 1365548-84-0(Hazardous Substances Data)

Upstream product

• 1698-16-4 10-bromo-7H-benzo[c]carbazole 
• 29874-83-7 2-chloro-4-phenylquinazoline 
• 1365548-83-9 C₃₀H₁₉N₃ 
• 607-68-1 2,4-dichloroquinazoline 
• 98-80-6 phenylboronic acid 

Downstream Products

• 1365548-86-2 C₃₀H₂₀BN₃O₂ 
• 1365548-87-3 C₄₈H₃₀N₄ 

Relevant articles and documents

Organic compounds and application thereof

The invention belongs to the technical field of organic photoelectric materials, and particularly relates to organic compounds and an application thereof. The parent nucleus structure of fused carbazole can remarkably improve the hole injection and transmission capacity of the compounds, so the hole mobility is effectively improved; when the parent nucleus structure of the fused carbazole is connected with an electron-withdrawing fragment, so the obtained compounds are bipolar compounds, and can be used as a luminescen layer host material, so that the charge balance is facilitated, and the very high light-emitting efficiency is realized; and when the parent nucleus structure of the fused carbazole is connected with an aromatic ring fragment, the obtained compounds can be used as a hole type material to be matched with an electronic host material in a double-host luminescent material, so the compounds can realizes a high luminescent efficiency due to high self hole mobility, and have excellent performances. A preparation technology of the compounds has the advantages of simplicity, easiness in implementation, easily available raw materials, and suitableness for mass production and amplification.