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

• 19261-06-4 4-hydroxydibenzofuran 
• 137959-93-4 3,3'-Diiododiphenylene oxide 
• 873974-43-7 1-bromodibenzofuran-4-ol 
• 86607-81-0 4-nitrodibenzo[b,d]furan 
• 100124-06-9 4-dibenzofurylboronic acid 
• 50548-37-3 N-(4-dibenzofuranyl)acetamide 
• 1374116-16-1 4-nitrosodibenzo[b,d]furan 
• 89827-45-2 4-bromodibenzofuran 
• 1399050-09-9 4-azidodibenzo[b,d]furan 
• 667937-27-1 4,6-dinitro-dibenzofuran 
• 854395-98-5 6-nitro-dibenzofuran-4-ylamine 
• 132-64-9 dibenzofuran 
• 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 
• 1381986-21-5 5,13-dihydro-5,5-dimethylbenzofuran[3,2-c]acridine 
• 1438401-13-8 N-(4-(tert-butyl)phenyl)dibenzo[b,d]furan-4-amine 

Relevant articles and documents

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Synthesis and Bond Activation Chemistry of Palladium(II) Pincer Complexes with a Weakly Coordinating Side Arm

A series of Pd(II) aryl complexes of a PNO-type pincer ligand bearing a weakly coordinated benzofuran side arm has been prepared. Crystallographic studies showed very long Pd-O distances of more than 2.3 ?, which is significantly longer than the Pd-O distances in structurally similar PNO-Pd complexes with an exocylic oxygen donor. Crystallographic and 19F NMR solution studies of complexes containing electron-donating (OMe) and electron-withdrawing (CF3) substituents in the position para to the benzofuran oxygen atom revealed the dependence of the Pd-O interactions on the nature of the aromatic group at the Pd center. The ability to influence these interactions by changing the electron density at the metal was demonstrated in the stoichiometric Sonogashira-type cross-coupling reactions between the Pd complexes and phenylacetylene, which proceed via a reversible aromatization/dearomatization of the pincer ligand. Complexes with the electron-poor CF3 group showed higher reactivity in comparison to their electron-neutral or -rich analogues. DFT studies of these systems provided further mechanistic insight into the origin of the observed reactivity patterns.

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