50548-43-1

Basic information

• Product Name: 4-AMINODIBENZOFURAN
• Synonyms: 4-AMINODIBENZOFURAN;4-Dibenzofuranamine;Dibenzofuran-4-amine;dibenzo[b,d]furan-4-aMine;4-Dibenzofuranamine HCl;4-Dibenzofuranamine hydrochloride
• CAS NO: 50548-43-1
• Molecular Formula: C₁₂H₉NO
• Molecular Weight: 183.20596
• Mol File: 50548-43-1.mol
• Article Data: 12

Chemical Properties

• Melting Point: 113.5-114.5℃
• Boiling Point: 369.1 °C at 760 mmHg
• Flash Point: 177 °C
• Appearance: /
• Density: 1.283 g/cm³
• Vapor Pressure: 1.21E-05mmHg at 25°C
• Refractive Index: 1.755
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 3.51±0.30(Predicted)
• CAS DataBase Reference: 4-AMINODIBENZOFURAN(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINODIBENZOFURAN(50548-43-1)
• EPA Substance Registry System: 4-AMINODIBENZOFURAN(50548-43-1)

Safety Data

• Hazardous Substances Data: 50548-43-1(Hazardous Substances Data)

Usage

General Description

4-Aminodibenzofuran is a chemical compound with the molecular formula C14H11NO. It is a white solid substance that is used in organic synthesis and has potential applications in pharmaceutical and material science research. It has been identified as a mutagen and may be toxic if inhaled, ingested, or absorbed through the skin. It is important to handle this compound with care and follow appropriate safety precautions when working with it in a laboratory setting. Additionally, its potential impact on the environment and human health should be carefully considered when using or disposing of 4-Aminodibenzofuran.

InChI:InChI=1/C12H9NO/c13-10-6-3-5-9-8-4-1-2-7-11(8)14-12(9)10/h1-7H,13H2

Upstream product

• 132-64-9 dibenzofuran 
• 100124-06-9 4-dibenzofurylboronic acid 
• 1374116-16-1 4-nitrosodibenzo[b,d]furan 
• 89827-45-2 4-bromodibenzofuran 
• 1399050-09-9 4-azidodibenzo[b,d]furan 
• 50548-37-3 N-(4-dibenzofuranyl)acetamide 
• 667937-27-1 4,6-dinitro-dibenzofuran 
• 854395-98-5 6-nitro-dibenzofuran-4-ylamine 
• 19261-06-4 4-hydroxydibenzofuran 
• 137959-93-4 3,3'-Diiododiphenylene oxide 
• 86607-81-0 4-nitrodibenzo[b,d]furan 
• 873974-43-7 1-bromodibenzofuran-4-ol 
• 67-62-9 O-Methylhydroxylamin 

Downstream Products

• 574-83-4 dibenzofuran-4-yl-(3-trifluoromethyl-benzyliden)-amine 
• 50548-37-3 N-(4-dibenzofuranyl)acetamide 
• 174187-07-6 7-Amino-2,3-tetramethylenebenzofurane 
• 1332882-14-0 1-(1,3-diisopropyldibenzo[b,d]furan-4-yl)-2-phenyl-4,5-dihydro-1H-imidazole 
• 1332882-15-1 1-(1,3-diisopropyldibenzo[b,d]furan-4-yl)-2-phenyl-1H-imidazole 
• 1318338-47-4 N-([1,1‘-biphenyl]-4-yl)dibenzo[b,d]furan-4-amine 
• 111091-95-3 sulfanilic acid dibenzofuran-4-ylamide 
• 42747-98-8 4-nitro-5-trans-styryl-thiophene-2-carboxylic acid methyl ester 
• 50548-39-5 1-bromodibenzo[b,d]furan-1-amine 
• 54470-37-0 Dibenzofuran-1-carboxylic acid 
• 50548-45-3 1-bromodibenzo[b,d]furan 
• 50548-40-8 1-aminodibenzofuran 

Relevant articles and documents

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Synthesis method of 4-aminooxyfluorene

The present invention discloses a method of synthesis of 4- aminooxyfluorene, in a solvent, oxene reacts with an organic base, nitrite to form 4-nitrosooxyfluorene, and then in the presence of a reducing agent, the nitroso is reduced to amino, to obtain the target product 4-aminooxyfluorene. The present invention by a strong base (sodium or potassium alcohol), nitrites and reducing agents, after two steps of reaction to synthesize 4-aminooxyfluorene, the reaction conditions are mild, simple, raw materials are inexpensive and readily available, less reaction by-products, high product yield, is conducive to industrial production.

An electroluminescent compound and an electroluminescent device comprising the same

The present invention relates to organic light emitting compounds represented by chemical formula 1-1 to chemical formula 1-2. An organic electroluminescent device using the same has excellent light emitting efficiency and can be driven at low voltage, thereby having improved power efficiency and long life characteristics.COPYRIGHT KIPO 2015