26608-06-0

Basic information

• Product Name: 3-Bromodibenzofuran
• Synonyms: NSC 167387;3-Bromodibenzofura;Dibenzofuran, 3-bromo-
• CAS NO: 26608-06-0
• Molecular Formula: C₁₂H₇BrO
• Molecular Weight: 247
• Product Categories: OLED
• Mol File: 26608-06-0.mol
• Article Data: 20

Chemical Properties

• Melting Point: 232-233℃
• Boiling Point: 343.8°Cat760mmHg
• Flash Point: 161.7°C
• Appearance: /
• Density: 1.4587 (rough estimate)
• Vapor Pressure: 0.000136mmHg at 25°C
• Refractive Index: 1.5290 (estimate)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-Bromodibenzofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Bromodibenzofuran(26608-06-0)
• EPA Substance Registry System: 3-Bromodibenzofuran(26608-06-0)

Safety Data

• Hazardous Substances Data: 26608-06-0(Hazardous Substances Data)

Usage

Chemical Properties

3-Bromodibenzofuran is a white crystal-Powder at 20°C. 3-Bromodibenzofuran can be used to synthesize a phosphorescent iridium complex containing a 3-phenylpyridazine structure.

Uses

3-Bromodibenzo[b,d]furan is a useful research chemical.

InChI:InChI=1/C12H7BrO/c13-8-5-6-10-9-3-1-2-4-11(9)14-12(10)7-8/h1-7H

Upstream product

• 4106-66-5 3-aminodibenzofuran 
• 132-64-9 dibenzofuran 
• 120612-68-2 diazotiertes 2-Amino-diphenylenoxyd 
• 872287-84-8 4-bromo-2-hydroxy-benzenediazonium betaine 
• 38191-34-3 2-amino-5-bromophenol 
• 2688-84-8 2-phenoxyaniline 
• 108-95-2 phenol 
• 1493-27-2 ortho-nitrofluorobenzene 
• 2216-12-8 1-nitro-2-phenoxy-benzene 
• 861605-94-9 2-phenoxy-4-bromobenzoic acid 
• 21849-89-8 4′-bromo-[1,1′-biphenyl]-2-ol 
• 106-37-6 1.4-dibromobenzene 
• 89466-08-0 2-hydroxyphenyl boronic acid 
• 1285719-48-3 4-bromo-2-fluoro-2'-methoxybiphenyl 

Downstream Products

• 29021-91-8 dibenzo[b,d]furan-3-carboxylic acid 
• 2786-05-2 dibenzofuran-4-carboxylic acid 
• 20279-16-7 3-hydroxydibenzofuran 
• 67019-91-4 3,7-dibromodibenzo[b,d]furan 
• 65489-80-7 2,8-dibromodibenzofuran 
• 1267248-41-8 3-(4-chlorophenyl)dibenzo[b,d]furan 
• 1705595-86-3 N-(3-dibenzofuranyl)-3-dibenzofuranamine 
• 1381985-63-2 6,6-dimethyl-6,11-dihydro-13-oxa-11-aza-indole[1,2-b]anthracene 

Relevant articles and documents

A thermally stable anthracene derivative for application in organic thin film transistors

A novel multifunctional anthracene derivative 2,6-bis(dibenzo[b,d]furan-3-yl)anthracene) (BDBFAnt), by coupling anthracene moiety with dibenzo[b,d]furan units attached to its peripheral position, has been designed and synthesized for application in OTFT devices. Introduction of dibenzo[b,d]furan units in OTFTs is the first example and is highly innovative due to their suitable carrier transport ability, excellent thermal stability, fine film-forming property, rigid planarity and outstanding fluorescence. The fabricated OTFTs demonstrate a decent hole mobility (3.0?cm2/V s) and favorable green solid fluorescence with excellent thermal stability (up to 220?°C), which expound on the great potential of our material in organic electronics.

Ir(iii)-Catalyzed direct C-H functionalization of N -phenylacetamide with α-diazo quinones: A novel strategy for producing 2-hydroxy-2′-amino-1,2′-biaryl scaffolds

α-Diazo quinones were applied in an Ir(iii)-catalyzed direct C-H functionalization assisted by N-phenylacetamide for the construction of highly functionalized 2-hydroxy-2′-amino-1,1′-biaryl scaffolds in good to excellent yields. This strategy features ope

NOVEL TRIAZINE COMPOUND, AND ORGANIC ELECTRONIC ELEMENT AND PLANT-GROWING LIGHTING THAT USE THE SAME

PROBLEM TO BE SOLVED: To provide a triazine compound which has a high triplet energy level and excellent heat resistance, and can be used as an organic electronic element material realizing an element with high efficiency, low voltage and a long life. SOLUTION: In the triazine compound, as represented by the general formula [1] in the figure, a triazine backbone moiety is linked to a dibenzofuran or dibenzothiophene backbone moiety via a biphenyl backbone moiety, where X is an oxygen atom or sulfur atom. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPO&INPIT