1383607-08-6

Basic information

• Product Name: 6-phenylbenzo[b]naphtho[1,2-d]furan
• Synonyms: 6-phenylbenzo[b]naphtho[1,2-d]furan
• CAS NO: 1383607-08-6
• Molecular Weight: 294.353
• Mol File: 1383607-08-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 6-phenylbenzo[b]naphtho[1,2-d]furan(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenylbenzo[b]naphtho[1,2-d]furan(1383607-08-6)
• EPA Substance Registry System: 6-phenylbenzo[b]naphtho[1,2-d]furan(1383607-08-6)

Safety Data

• Hazardous Substances Data: 1383607-08-6(Hazardous Substances Data)

Usage

General Description

6-phenylbenzo[b]naphtho[1,2-d]furan is a chemical compound that belongs to the class of polycyclic aromatic hydrocarbons (PAHs). It is a complex molecule consisting of multiple benzene rings fused together in a unique arrangement. 6-phenylbenzo[b]naphtho[1,2-d]furan is of interest to researchers due to its potential biological and environmental implications. PAHs are known to be ubiquitous in the environment, and some of them are considered to be carcinogenic. Therefore, understanding the properties and behavior of 6-phenylbenzo[b]naphtho[1,2-d]furan is important for assessing its potential impact on human health and the environment. Additionally, its unique structure and properties may have potential applications in various fields, such as materials science and pharmaceuticals.

Upstream product

• 24243-67-2 1,3-diphenyl-2-naphthol 
• 108-95-2 phenol 
• 452962-66-2 3-(2-iodophenyl)benzofuran 
• 452962-75-3 1-(2-iodophenyl)-2-phenoxyethanone 
• 98-80-6 phenylboronic acid 
• 1382763-56-5 1-(2-fluorophenyl)-2-methoxynaphthalene 
• 1264712-17-5 1-(2-fluorophenyl)naphthalen-2-ol 
• 205-39-0 benzo[b]naphtho[1,2-d]furan 
• 573-97-7 1-bromo-2-naphthol 
• 3401-47-6 1-bromo-2-methoxynaphthalene 
• 1993-03-9 o-fluorophenylboronic acid 
• 108-86-1 bromobenzene 
• 1382763-54-3 (benzo[b]naphtho[1,2-d]furan-6-yl)boronic acid 

Relevant articles and documents

Intramolecular Electrophilic Cyclization Approach to 6-Substituted Naphtho[2,1- b]benzofurans: Novel Dual-State Emissive Fluorophores with Blue Emission

A regiospecific synthesis of naphtho[2,1-b]benzofurans with a substituent at the C6 position was achieved via intramolecular 6-endo-dig electrophilic cyclization under acidic conditions to construct the central aromatic C ring. Screening of the synthesize

LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE, AND LIGHTING DEVICE

A novel light-emitting element is provided. A light-emitting element with a long lifetime is provided. A light-emitting element with high emission efficiency is provided. A novel organic compound is provided. A novel organic compound having a hole-transport property is provided. A novel hole-transport material is provided. A hole-transport material including an organic compound having a substituted or unsubstituted benzonaphthofuran skeleton and a substituted or unsubstituted amine skeleton is provided. A light-emitting element using the hole-transport material is provided. An organic compound in which an amine skeleton including two aromatic hydrocarbon groups having 6 to 60 carbon atoms is bonded to the 6- or 8-position of the benzonaphthofuran skeleton is provided.

HETEROCYCLIC COMPOUND, LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, ELECTRONIC DEVICE, AND LIGHTING DEVICE

A novel heterocyclic compound that can be used as a host material in which a light-emitting substance is dispersed. A light-emitting element having a long lifetime. A heterocyclic compound in which a substituted or unsubstituted dibenzo[f,h]quinoxalinyl group is bonded to a substituted or unsubstituted arylene group having 6 to 25 carbon atoms which is bonded to any one of the 8-11 positions of a substituted or unsubstituted benzo[b]naphtho[1,2-d]furan skeleton.